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Reinterpretation of evidence advanced for neo- oogenesis in mammals, in terms of a finite oocyte reserve
Journal of Ovarian Researchvolume 4, Article number: 1 (2011)
The central tenet of ovarian biology, that the oocyte reserve in adult female mammals is finite, has been challenged over recent years by proponents of neo-oogenesis, who claim that germline stem cells exist in the ovarian surface epithelium or the bone marrow. Currently opinion is divided over these claims, and further scrutiny of the evidence advanced in support of the neo- oogenesis hypothesis is warranted - especially in view of the enormous implications for female fertility and health. This article contributes arguments against the hypothesis, providing alternative explanations for key observations, based on published data. Specifically, DNA synthesis in germ cells in the postnatal mouse ovary is attributed to mitochondrial genome replication, and to DNA repair in oocytes lagging in meiotic progression. Lines purported to consist of germline stem cells are identified as ovarian epithelium or as oogonia, from which cultures have been derived previously. Effects of ovotoxic treatments are found to negate claims for the existence of germline stem cells. And arguments are presented for the misidentification of ovarian somatic cells as de novo oocytes. These clarifications, if correct, undermine the concept that germline stem cells supplement the oocyte quota in the postnatal ovary; and instead comply with the theory of a fixed, unregenerated reserve. It is proposed that acceptance of the neo- oogenesis hypothesis is erroneous, and may effectively impede research in areas of ovarian biology. To illustrate, a novel explanation that is consistent with orthodox theory is provided for the observed restoration of fertility in chemotherapy-treated female mice following bone marrow transplantation, otherwise interpreted by proponents of neo-oogenesis as involving stimulation of endogenous germline stem cells. Instead, it is proposed that the chemotherapeutic regimens induce autoimmunity to ovarian antigens, and that the haematopoietic chimaerism produced by bone marrow transplantation circumvents activation of an autoreactive response, thereby rescuing ovarian function. The suggested mechanism draws from animal models of autoimmune ovarian disease, which implicate dysregulation of T cell regulatory function; and from a surmised role for follicular apoptosis in the provision of ovarian autoantigens, to sustain self-tolerance during homeostasis. This interpretation has direct implications for fertility preservation in women undergoing chemotherapy.
Since the mid-twentieth century, the prevailing principle in mammalian oocyte biology has been that female reproductive capacity is defined absolutely by the number and quality of primordial follicles having developed in the ovary by the neonatal period . Acceptance of this principle was predicated on empirical evidence: that the mechanism of oocyte formation entails expansion from a relatively small population of primordial germ cells (PGC) in the foetal period, to provide a massive reserve of primordial follicles at birth [2, 3]; and that gradual depletion of that reserve in the adult by atresia and ovulation leads to reproductive senescence and cessation or, specifically in humans, the menopause . The predicted and observed consequence of this theory is that oocytes ovulated later in the reproductive period are of inherently poorer quality due to cellular defects, chromosomal abnormalities and functional deteriorations that accumulate with age [5, 6].
Recent years have seen repeated challenges to this orthodoxy, constituting a revival of the concept of de novo oogenesis in the adult ovary, or neo- oogenesis. The key studies and ensuing discourse are summarised as follows. Diverse groups have purported evidence for neo-oogenesis in mice, from germline stem cells existing specifically in the ovarian epithelium [7–11]. Moreover, claims were made that female germline stem cells originate at a site extraneous to the ovary, namely the bone marrow, and are transported to the ovary via the circulatory system [12, 13]: a scenario that would represent a radical transformation of the established theory of germline specification [2, 3]. The study of Eggan et al. , using parabiosis between female mice to demonstrate that ovulated oocytes are not derived from transfused precursors, is significant in countermanding claims for the provision of oocytes via the circulation . But this was in turn refuted by Tilly et al. , who deduced evidence for crossengraftment of oocytes supplied from a parabiont, in a robust defense of the neo- oogenesis concept. Abban and Johnson  find further support for neo- oogenesis in the derivation of so-called "female germline stem cell" (FGSC) lines by Zou et al. . Pacchiarotti et al.  also claim the establishment of ovarian germline stem cell lines, and endorse the neo-oogenesis hypothesis. Meanwhile, cogent arguments were made against the replenishment of oocytes, from statistical analysis of the follicle pool over the reproductive period in mice [17, 18]; and a recent study involving mathematical modelling of the ovarian reserve found no evidence to support the occurrence of neo-oogenesis in humans .
To date, a consensus has yet to emerge regarding the validity of neo-oogenesis in relation to adult female mammals, and forthright opinions have been expressed in favour of [13, 15, 16, 20] and against [14, 17, 21–24] the hypothesis. Furthermore, qualified support has been expressed for the occurrence of neo-oogenesis in mice, but not in humans . In another permutation of the hypothesis, germline stem cells exist in adult mouse ovaries but are quiescent under physiological conditions , functionally contributing to the oocyte reserve only in response to ovotoxic damage .
Thus, the debate continues and a consensus has yet to emerge. Further scrutiny of the evidence advanced in support of the neo- oogenesis hypothesis therefore is warranted - particularly in view of the enormous implications it holds for female fertility and health. Moreover, establishing the mechanism of oocyte allocation is fundamentally important to developmental, comparative and reproductive biology. This article contributes arguments against neo-oogenesis, revisiting underlying assumptions and providing alternative explanations (summarised in Table 1) for observations advanced - and maintained - as key by advocates of the hypothesis, adding to the considerable body of criticisms already levied. If the neo- oogenesis hypothesis is incorrect, an alternative explanation is required for a significant finding made by its proponents: the restoration of fertility by bone marrow transplantation (BMT) to chemotherapy (CT) treated mice.
2. Evidence advanced for neo- oogenesis
(i) BrdU-incorporation by germ cells located in the ovarian surface epithelium
A primary observation made in mice by proponents of neo- oogenesis has been the incorporation of the thymidine analogue, 5-bromo-2-deoxyuridine (BrdU), by germ cells located in the ovarian surface epithelium (OSE), as detected by immunocytochemistry using anti-BrdU monoclonal antibody: this was interpreted as evidence for mitotic germ cells [7, 10], with the OSE functioning as a classical, germinal epithelium [7–9, 11]. Johnson et al.  discounted the alternative possibilities that BrdU-incorporation arose from either mitochondrial (mt) DNA replication or DNA repair in oocytes, on the basis that "the degree of BrdU incorporation observed in cells due to either of these processes is several log orders less than that seen during replication of the nuclear genome during mitosis." This assumption is invalid because the immunocytochemical technique used is both likely and sensitive enough to detect (a) mtDNA synthesis and (b) DNA repair in meiotically arrested oocytes, as discussed below.
(a) Anti-BrdU antibody detection of mtDNA synthesis
In studies using anti-BrdU immunocytochemistry to observe cell proliferation, BrdU incorporation into mtDNA may be discounted where mtDNA constitutes a minor fraction of total cellular DNA (< 0.2% in the case of L cells, or 50 mtDNA molecules per cell ). Here, anti-BrdU antibody is saturated by binding to BrdU-substituted nuclear DNA (nDNA), and the relatively much lower incorporation of BrdU into mtDNA goes undetected . However, early studies established that mtDNA replication occurs autonomously to that of nDNA in cultured cells; and that in the absence of nDNA replication, mtDNA can be labelled with BrdU to a high specific activity [29, 30] that is detectable by anti-BrdU immunocytochemistry, with short incorporation periods (1-2 h) commensurate with mtDNA replication times . It is therefore argued that for mammalian oocytes in particular, mtDNA synthesis would be readily detectable: not only is nDNA replication absent, but also the number of mitochondria is considerable, increasing from <200 in PGC to ~6,000 in the resting oocyte of the primordial follicle . The mouse secondary oocyte contains ~92,000 mtDNA copies . Hence, it is feasible that the aforementioned studies of Johnson et al.  and Zou et al.  would have detected in situ mtDNA incorporation in prophase-arrested oocytes.
This deduction is supported in both studies [7, 10] by the apparent co-localisation of immunofluorescence for BrdU with mouse VASA-homologue (Mvh), the germ cell-specific protein that is cytoplasmic in location . For example, in the report of Johnson et al. , Figure two 'd' shows a clearly defined oocyte at the ovarian surface stained with anti-BrdU immunofluorescence (red signal) co-localised with anti-Mvh immunofluorescence (green signal) to give a strong, combined yellow signal dispersed throughout the cytoplasm. (In cultured cells  and oocytes , newly synthesised mtDNA is initially located at a perinuclear location, adjacent to the nuclear boundary, and becomes dispersed in the periphery of the cell with time.) If, as claimed by Johnson et al. , BrdU incorporation represented nDNA replication, this would require the cell to have attained prometaphase (at which stage the nuclear membrane breaks down) so that BrdU incorporation would be detectable in the cytoplasm. However, it is highly unlikely that during the 1 h labelling period the cell could have exited S-phase and transited G2 and prophase, and so nuclear DNA replication can be discounted. In the report of Zou et al. , Figure S1 shows nuclear staining for anti-BrdU immunofluorescence (green signal) in the nuclei of primary oocytes in 'a', but also co-localisation with anti-Mvh immunofluorescence (red signal) to give a yellow signal in 'a', 'b', 'd' and 'e'. Moreover in 'a', the yellow signal is closely juxtaposed to the nuclear boundary, in keeping with mtDNA synthesis at this location occurring simultaneously with nuclear incorporation. To summarise, it is inferred that the examples of BrdU-labelled germ cells presented by Johnson et al.  and Zou et al.  provide direct evidence for mtDNA synthesis occurring in oocytes located at the surface of the neonatal [7, 10] and adult  mouse ovaries.
(b) Anti-BrdU antibody detection of DNA recombination and repair
The condition allowing detection of mtDNA synthesis by in situ BrdU immunocytochemistry, namely an absence of nDNA replication , would also allow detection of nDNA synthesis arising from recombination and repair by the same technique. Accordingly, in situ BrdU immunocytochemistry has been used to reveal DNA repair in mammalian cells . And the detection of stretches of single-stranded BrdU-substituted DNA at sites of meiotic recombination in mouse spermatocytes illustrates the sensitivity of this method .
In mammals, the meiotically arrested oocyte contains the enzymatic capacity for DNA repair pathways , and circumstantial evidence for this activity was obtained by Oktay et al.  from expression of the DNA-repair associated protein, PCNA, in growing and atretic rat oocytes. Although the extent of DNA synthetic activity arising from DNA recombination and repair in oocytes at earlier stages is unclear, it may not be negligible. The meiotic process in the oocyte is highly error prone , which leads to high rates of elimination of immature oocytes, especially at diplotene in the neonatal period . Meiotic recombination occurs during the pachytene stage of prophase I, prior to diplotene arrest; and in the mouse this latter stage is reached by most oocytes by day 5 postnatal . As meiotic prophase I is asynchronous, the temporal window for meiotic recombination extends into the neonatal period: non-apoptotic, pre-diplotene (zygotene and pachytene) oocytes have been noted to persist for at least 2 d after birth, with 7.4% of oocytes in pachytene on day 2 postnatal . This is a most relevant finding, which was attributed by Ghafari and colleagues  to a prolongation of early stages of meiosis in a proportion of oocytes, necessitated by ongoing DNA recombination or repair. By inference, such a population of pre-diplotene stage oocytes engaged in recombination or repair activities would be readily detectable by in situ BrdU immunocytochemistry, in the neonatal mouse ovary. The distinct, nuclear staining for BrdU in the oocyte of Figure two 'e' of Johnson et al. , and in oocytes in Figure S1 ('a') of Zou et al. , could therefore be attributed to DNA recombination or repair.
In summary, the immunofluorescent detection of BrdU incorporation into oocytes of the neonatal mouse [7, 10] can be ascribed to mtDNA synthesis where BrdU incorporation is cytoplasmic, and to DNA recombination and repair where incorporation is nuclear, rather than to replicative nDNA synthesis alone. These alternative explanations may be relevant also to the detection of thymidine incorporation in diplotene and atretic oocytes in the ovaries of adult prosimian primates [42, 43]. Crone and Peters  previously documented the incorporation of tritiated thymidine into the nuclei of early diplotene oocytes of mice injected in the neonatal period. These labelled oocytes were in nascent follicles located centrally in the ovary, and were cleared within a few days. The authors considered the phenomenon most likely represented abnormal DNA synthesis and repair in degenerating oocytes, whose frequency may have been underestimated owing to the lack of sensitivity of their technique. These considerations provoke the question, what is the reason for the location of BrdU-labelled oocytes in OSE [7, 10]? Perhaps these studies present a snapshot in a poorly understood process contributing to oocyte attrition in both mouse and human - the extrusion of oocytes from the ovarian surface and into the peritoneal cavity [24, 45], which was postulated by Motta et al.  to occur beyond the neonatal period, to puberty. Could these surface oocytes be defective, as postulated by Crone and Peters ?
(ii) Cultured OSE gives rise to "oocyte-like" cells
Following the deduced existence of mitotic germ cells in the OSE (above), Bukovsky et al.  and Virant-Klun et al.  endeavoured to culture OSE derivatives, and subsequently reported the production of "oocyte-like" cells in vitro. Two major limitations are common to both studies.
(a) The criteria used to denote an "oocyte-like" phenotype [8, 9] are morphological, namely: cells with large and rounded morphology in which a large or no nucleus is visible, and which may be surrounded by a structure resembling a zona pellucida (ZP). However, the photomicrographs presented may instead depict those general features of cells undergoing apoptosis, necrosis or - especially - oncosis , namely: cell swelling, plasma membrane breakdown, and swollen or lysed nuclei. Structures described as "developing zona pellucida" [8, 9] may reflect cellular swelling, membrane rupture and lysis, and spillage of cytoplasm ; the "germinal vesicle" [8, 9], nuclear swelling ; and "germinal vesicle breakdown" [8, 9], karyolysis . These considerations underline the importance of validating putative oocytes by immunocytochemical and molecular techniques, rather than by morphological criteria. The attempt by Bukovsky et al.  to detect ZP-antigenicity in these cells by immunofluorescence is marred throughout by a high background of staining of the cytoskeleton, which is probably an artefact of desiccation arising from the unconventional step of air-drying cells overnight, prior to fixation. Desiccation and cell death occur extremely rapidly under these conditions [47, 48], with interim activation of survival and death pathways . Regarding the deduced ZP-antigenicity of OSE-derived "germ-like" cells as detected using PS1 antibody , it should be noted that Skinner and Dunbar  considered their antibody to be non-specific for ZP proteins as it recognises a carbohydrate moiety present on the apical surface of the OSE.
(b) It is immediately apparent that the culture systems of Bukovsky et al.  and Virant-Klun et al.  are relatively very simple, without addition of the growth factors, cytokines or feeder-cell support that usually are essential to the growth of pluripotent germline cells or ES cells. In fact, the growth of embryonic or germline stem cells under these conditions would be unprecedented. What cells, therefore, could constitute the proliferating populations in these studies?
As cultures were obtained by the conventional technique of scraping of the OSE, the heterogeneity of cells should be considered: an estimated 98% of cells obtained in this way are ovarian epithelial cells , and contaminants include extraovarian mesothelial cells, endothelial cells, ovarian somatic and mesenchymal cells, and immune cells . Moreover, cultured OSE demonstrates an epitheliomesenchymal phenotype with contractile functions, and the capacity to differentiate into stroma, granulosa cells or Müllerian epithelia, reflecting its role in vivo as a dynamic tissue involved in post-ovulatory tissue repair and remodelling . Granulosa cells express Oct4 and are multipotent, differentiating into neurons, chondrocytes and osteoblasts . Therefore, in the absence of data from clonal cell analysis, and of unambiguous validation by stem cell-specific markers (see below), the claims of Bukovsky et al.  and Virant-Klun et al.  for spontaneous in vitro differentiation of germline stem cells into cells of mixed phenotype should be regarded with caution.
The cell types cultured by Virant-Klun et al.  from OSE scrapings from postmenopausal women, termed "putative stem cells", "oocyte-like", or "embryonic", may be re-identified from information in the literature. "Putative stem cells" were identified morphologically as round cells, 2-4 μm in diameter, located below or above the OSE . However, the possibility arises that these are small immune cells, e.g. lymphocytes or plasma cells, which are seen located above and below the OSE in ovarian sections . After enrichment by differential centrifugation, these "putative stem cells" proliferated in culture . Plasma cells, also, can be cultured easily in simple media , but the presence of this cell type as a culture contaminant was not considered . Virant-Klun et al.  stated that the proliferating "putative stem cells" generated adherent oocyte-like cells, 20-95 μm in diameter, with ZP-like, germinal vesicle-like and polar body-like structures that were ascribed to an oocyte nature. However as stated above, these structures could arise from oncosis in any of the cell types being cultured, causing cell swelling, karyolysis and cytoplasmic leakage. In their cultures, Virant-Klun and colleagues  also describe the formation of "embryoid body-like" and "blastocyst-like" structures, interpreted as products of parthenogenetic activation of oocyte-like cells. However, they are far less convincing in appearance than the (parthenogenetic) embryos demonstrated by Hübner et al.  to arise from ES cell differentiation into oocytes. Could there be an alternative explanation for the structures produced by Virant-Klun et al. ? The aggregates of cells termed "embryoid-body like" could arise from any cell type, rather than being diagnostic of embryoid bodies proper with their complex internal differentiation. And the vesicles formed by these aggregates with continued culture could arise from a contaminating epithelial cell type, such as OSE , which has the capacity to polarise and form impermeable junctions. The propensity to form vesicles in culture is a common property of epithelial cells from epithelial linings ; and the increased tendency of OSE to line clefts and inclusion cysts in the ovary, with increasing age, may be relevant here . Further clues to the identity of the cells can be gleaned from patterns of transcription: "putative stem cells" expressed OCT4, SOX-2, NANOG and C-KIT, and "blastocyst-like" structures expressed OCT4, SOX-2 and NANOG, from which an embryonic nature of the putative stem cells was inferred by Virant-Klun et al . However, a recent study by Song et al.  first showed that the trio of stem cell regulatory genes, Oct4, Sox-2 and Nanog, constitute markers for epithelial stem cells, whose function is vital to regeneration and tissue homeostasis: they are expressed during the regeneration of rat tracheal epithelium in vitro, specifically by epithelial stem cells in the G0 phase. Expression of Oct4 is associated also with a variety of types of epithelial stem cells, but not their differentiated derivatives . Moreover, human epithelial ovarian cancer cell lines and the multilayered structures, or spheroids, they form in suspension culture are known to highly express stem cell-specific genes, including OCT4, NANOG and NESTIN [60, 61]. It is therefore inferred that the OSE-derivative cultures of Virant-Klun et al.  comprise epithelial stem cells, which are responsible normally for maintaining the integrity of the OSE - a property that may be especially important in ovaries of post-menopausal women , used here. This inherent regenerative potential may be manifest in culture. Another feature is consistent with the presence of OSE in these cultures - the expression of C-KIT . In fact, both C-KIT and KIT LIGAND are expressed by human, normal OSE .
The importance of critically evaluating claims for the validation of cell lines as female (or ovarian) germline stem cells is further illustrated by the recent study of Pacchiarotti et al. . These authors reported the isolation and characterisation of germline stem-cell lines from ovaries of neonatal mice of the TgOG2 strain. (These mice carry an Oct4-GFP transgene where GFP expression is controlled by an Oct4 promoter sequence. They are considered in more detail in section 2.(iv).) Their main conclusions are as follows:
(a) Germline stem cells were identified at the ovarian surface, on the basis of their small size (10-15 μm) and expression of Oct4-GFP, Mvh, c-kit and SSEA-1. These cells were purported to transition into germ cells of intermediate size (20-30 μm), and subsequently into growing oocytes.
(b) Cell populations containing the putative stem cells were isolated from disaggregated suspensions of whole ovaries by fluorescence-activated cell sorting for Oct4-GFP expression, and propagated using a feeder-based culture system. It was deduced that the derived lines consisted of ovarian germline stem cells from their expression of germ-cell and stem-cell markers (namely, Gcna1, c-kit, Oct4, Nanog and GFR-α1).
(c) Further evidence for the status of these cells as germline stem cells was presented from the formation of "embryoid bodies" containing differentiated derivatives of the three germ layers, mesoderm (denoted by expression of Bmp-4 and troponin), ectoderm (Sox-1, Ncam, nestin) and endoderm (FoxA2, Gata-4); and the production of early stage oocytes during culture.
However, many of these assumed marker specificities are incorrect and the above conclusions are therefore unwarranted, as discussed in detail below. Rather, it is proposed that the cultures consisted of monolayers of OSE, together with a proportion of early oocytes and/or oogonia. That is, a complex co-culture system is envisaged containing both somatic and germ-cell types. It is notable that the culture medium used by Pacchiarotti et al.  was optimised for spermatogonial stem cells (SSC) , as was that employed by Zou et al.  for FGSC. These media are considered further in section 2.(v), as potentially being mitogenic for growth-arrested oogonia.
(a) Rather than providing direct evidence for germline stem cells, the localisation of small cells (≤15 μm) expressing Oct4, Mvh and SSEA-1, and subtending the OSE, is compatible with residual oogonia [64–66]. In fact, the authors acknowledged the likely existence of oogonia in these neonatal ovaries.
(b) These putative germline stem cell lines show a striking resemblance in morphology and growth characteristics (with a low mitotic rate) to previously established mouse and human OSE cell lines [67–69], growing in monolayers as epithelial colonies with cobblestone appearance, with a tendency towards multilayering at the centre. (Compare, for example, the cellular morphology in Figure three 'N' of Pacchiarotti et al.  with that of mouse OSE in Figure two 'A' of Roby et al.  and in Figure four 'B' of Szotek et al. .) Like established lines of mouse OSE cells at low passage , these putative stem cells lacked tumorigenicity in mouse xenograft systems. Furthermore, markers reportedly expressed by these cultures are not germline specific: GFR-α1 is expressed by OSE ; and co-expression of c-kit, Oct4 and Nanog was discussed in section 2.(ii), in the context of the OSE as a regenerative epithelium.
(c) Concerning the structures described as "embryoid bodies", patterns of gene expression were entirely consistent with OSE, as a mesoderm-derived, multipotent epithelium with stromal characteristics. For example, nestin  and Gata-4  are markers for OSE stem cells. FoxA2 is known to be expressed in uterine glands , and expression in this culture system may therefore be indicative of OSE cells undergoing Müllerian-type differentiation towards endometrioid cells . In short, the structures described resemble those spheroids that are formed by both normal OSE [68, 73] and ovarian cancer-derived cell lines .
Detection of Gcna-1 in these cell lines requires further comment, as this antigen is considered specific to the nuclei of germ cells in the neonatal and foetal gonad, from zygotene through pachytene stages of meiotic prophase. It is relevant that Alton and Taketo  observed immunocytochemical staining for Gcna1 in a large number of cells either in, or protruding from, the OSE in foetal mouse ovaries at 18.5 d.p.c., which was attributed to oocytes in the process of exfoliation. However, that those cells did not express Mvh  is incompatible with their identification as oocytes. It is therefore suggested that Gcna-1 may be expressed by OSE, especially during the neonatal period or in culture. Another germ cell-specific gene, VASA, is expressed by ovarian epithelial cancers, which arise from transformation of the OSE . Now that candidate stem cells for OSE have been identified by Szotek et al. , it will be of interest to determine if genes involved in germ-cell specification also are involved in normal epithelial regeneration, or differentiation. As well as increasing understanding of the etiology of ovarian epithelial cancers, this information will help clarify the origin of cell lines claimed to represent ovarian germline stem cells [8, 9, 11] on the basis of expression of germ-cell markers.
(iii) Busulphan-induced depletion of the follicle reserve
Recently, Tilly et al.  cited their findings from busulphan (BU) treatment of female mice as key evidence for neo- oogenesis, based on their understanding that this chemotherapeutic, alkylating agent targets replicative - and not postmeiotic - germ cells in females, as well as males. By their reasoning, inhibition of de novo oocyte formation by BU treatment leads to exhaustion of the oocyte reserve by normal processes during oestrus cycling: "Young adult female mice treated with busulfan exhibit a gradual loss of the entire primordial follicle reserve over a 3-wk period without a corresponding cytotoxic effect on primordial follicles . Such an outcome would be expected if busulfan were, as past studies contend , selectively eliminating replicative germ cells that support primordial oocyte formation. The net result would be the normal rate of follicle loss via atresia no longer partially offset by de novo follicle formation, leading to accelerated depletion of the follicle reserve without the need for a corresponding increase in the rate of oocyte death." However the major premise here, that BU targets only replicative (and, by definition, premeiotic) germ cells in both females and males without causing atresia in postmeiotic cells (oocytes and spermatids), is seen to be incorrect from what is discussed below. Furthermore, it is deduced that the data of Johnson et al.  provide direct evidence against neo-oogenesis, and against precursors to oocytes being supplied from bone marrow precursors. To this end, it is necessary to consider the known effects of BU on female and male, murine reproductive function.
(a) BU causes atresia in oocytes and disrupts folliculogenesis
Although early studies in the rat established that BU-treatment during pregnancy induces lethality in the replicative oogonia of the foetus [77, 78], substantial evidence indicates that the effects of BU are not confined to this stage. Burkl and Schiechl  observed that in the adult rat, chronic BU treatment is disruptive to the whole process of folliculogenesis: antral and secondary oocytes show diminished growth, with rapid and extensive degeneration; and younger follicles show abnormal development into distinct follicular structures with enlarged oocytes having only a single-cell layer of granulosa, correlating with late secondary or antral stages. These aberrant follicles were inferred to arise from inhibition of mitosis in the somatic cells, including granulosa cells. And in some of these single-layered structures, follicular fluid was seen to accumulate in a fissure-shaped antrum between the ZP and the follicular epithelium. (Such a hallmark of BU-induced ovotoxicity may be exemplified by the abnormal follicle in Figure four 'c' of Johnson et al. , to the upper left of the photomicrograph.) The work of Generoso et al.  informs of the gross effects on oocytes of a single administration of BU (or Myleran) in juvenile female mice: there is a dose-dependent, detrimental effect on fertility (at doses of 10-60 mg/kg i.p.) due to a progressive depletion of oocytes at the advanced as well as the earliest stages of development. Fertility is extinguished irreversibly after injection with 40 or 60 mg/kg; and at 40 mg/kg the total oocyte count diminished precipitously 7-14 d posttreatment.
In other words, and contrary to the claim by Johnson et al.  and Tilly et al.  that oocytes are refractory to the effects of BU, previous studies show that in the adult murine, BU exerts an immediate and lethal effect on late stage oocytes [79, 80] that is accompanied by an aplasia resulting from active destruction of the primordial follicle pool .
(b) Predicted mechanism of BU cytotoxicity in folliculogenesis, via suppression of c-kit/SCF signaling
Further insight into the mechanism of action of BU can be gained from its effects on male germline stem cells (i.e. spermatogonial stem cells (SSC)) and on haematopoietic stem cells (HSC). Tilly et al.  stated that SSC are depleted by BU treatment. However, the work of Choi and colleagues [81, 82] shows that the converse is true: SSC survive BU treatment in mice, while differentiating spermatogonia, meiotic spermatocytes and postmeiotic spermatids are depleted via apoptosis. A mechanism of action was deduced whereby BU induces loss of c-kit expression in these susceptible populations, with concomitant downregulation of c-kit/SCF signaling, leading to a block in G1 due to inhibition of PCNA synthesis. Meanwhile, the quiescent SSC are unaffected by BU due to their lack of c-kit expression, and spermatogenesis is fully restored eventually by these testis-repopulating cells . In other words, abrogation of c-kit function is central to the mechanism of action of BU on spermatogenesis. By extension, we can infer significant consequences of BU-induced downregulation of c-kit/SCF signaling for folliculogenesis. Hutt et al.  review evidence from mouse models that the paracrine c-kit/SCF signaling pathway is crucial for activation of primordial follicles, oocyte survival and growth, and maintenance of meiotic arrest in small antral follicles. (This is in addition to roles in PGC colonisation of the ovary, proliferation of oogonia, proliferation of granulosa cells, and recruitment of thecal cells.) For humans also, there is evidence for paracrine and autocrine roles of this pathway in primordial follicle assembly and throughout folliculogenesis. Functional studies directly implicate c-kit in controlling folliculogenesis: antibody-induced blockade of c-kit causes attenuation of follicular development in neonatal and adult mice , and promotion of oocyte death in vitro . Kissel et al.  documented arrested development of follicles in juvenile c-kit mutant mice, with mainly single-layered follicles predominating (cf. abnormal follicles of Burkl & Schiechl , described above). Therefore, functional c-kit is prerequisite to the survival and development of preovulatory follicles, and to granulosa cell proliferation. The documented effects of BU on developing and antral follicles  are now interpretable in terms of downregulation of c-kit/SCF signaling. The deduction of Yoshida et al.  is relevant, that in haematopoiesis, hair follicle melanogenesis, and spermatogenesis, c-kit function is required for differentiation and survival of cells that have advanced from stem cell pools, but not for the maintenance of quiescent stem cells. This is fully substantiated for spermatogenesis by the studies of Choi et al. , described above.
(c) BU induces transient myelosuppression with irreversible sterility
Lastly, in view of the bone marrow-derived oocyte precursors proposed by Johnson et al. , the effect of BU as a chemotherapeutic agent on haematopoiesis should be considered. Would BU treatment impinge on a precursor population from that source? The dose of BU used by Johnson et al. , namely 2 injections at 20 mg/kg i.p., 10 days apart, is not myeloablative but would cause transient myelosuppression, which is resolved in the strain used (C57BL/6) by 4-5 weeks . (A myeloablative dose is 150 mg/kg .) For HSC, therefore, long-term repopulating stem cells would not be deleted by this BU dosage . If oocytes are BM-derived, resumption of haematopoiesis should lead to restoration of fertility in BU-treated mice. However, fertility was extinguished in the studies of Johnson et al. , as it was also in the study of Generoso et al.  with similar BU dosages (see (a), above). Therefore, the absence of restoration of fertility in BU-treated mice is taken as direct evidence against BM as a source of precursors for neo-oogenesis [7, 12].
In summary, the data of Johnson et al.  on BU treatment of female mice causing aplasia and ovarian failure are interpretable entirely by cytotoxicity to early and late stage oocytes, and disruption of folliculogenesis. Evidence from other systems (spermatogenesis, haematopoiesis) implicates BU-induced down regulation of c-kit/SCF signaling, the function of which pathway is critical to folliculogenesis.
(iv) Oocyte precursors from peripheral blood
Johnson et al.  modified their concept of neo- oogenesis to specify that oocyte progenitors are supplied to the ovary by the bone marrow via the circulatory system. This came from experiments on wild type (wt) and Atm-deficient (Atm-/-) mice in which sterile, depleted ovaries were reportedly repopulated with oocytes derived from EGFP-labelled progenitors, following peripheral blood cell transplantation (PBCT). Subsequently there have been other reports of successful engraftment of donor somatic cells as oocytes following CT and BMT , with the provisos that: only a low percentage of designated immature oocytes are donor-derived (around 0.1% of total oocytes in recipients) when bone marrow or peripheral-blood cells are transplanted; designated follicles are never observed beyond preantral stages (i.e. maturing antral or Graafian follicles); and donor cell-derived mouse offspring have never been produced. (Meanwhile, other attempts to reproduce these findings have proved entirely unsuccessful [14, 23].) The general consensus is that any de novo follicles do not undergo ovulation, although they may support the depleted ovary . What, therefore is the functional relevance of this proposed, renewing population of early-stage oocytes? Arguments leading to alternative identities for those cells designated as de novo, immature oocytes [12, 13] are given below.
(a) Identification of de novo oocytes relies on germ-cell specificity of Oct4 expression
Attention is drawn here to the hypothesis of Eggan et al.  that bone marrow-derived cells might co-express germ cell-specific markers, and that the cells designated as immature oocytes by Johnson et al.  could have been misidentified. This hypothesis subsequently was refuted by Lee et al.  on the basis that expression of the transgene, Oct4-EGFP, in the TgOG2 line of transgenic mice is restricted to the germ line; furthermore, peripheral blood cells expressing the panleukocyte marker, CD45, expressed neither EGFP nor germ cell markers. However, those cells designated as oocytes were not examined for haematopoietic markers in situ, which analysis would have been definitive. The hypothesis of Eggan et al.  is developed further here, by considering the possible involvement of one particular CD45+ and SSEA1+ cell type, the macrophage, which is a differentiated derivative of circulating monocytes. Inspection of photomicrographs presented by Tilly et al.  as depicting de novo oocytes in follicular nests reveals centrally within those nests large, non-spherical (and EGFP positive) cells with irregular nuclei, cytoplasmic inclusions and numerous, clear cytoplasmic vacuoles (see Figure one, right-hand panel, in Tilly et al. ): these features are highly reminiscent of macrophages rather than oocytes. Figure two ' B' in Lee et al.  shows a similar EGFP-positive cell within a follicle, dissimilar in morphology to an oocyte, with cytoplasmic inclusions resembling phagocytised granulosa cells (one of which appears to be membrane enclosed). Johnson et al.  contend that their female germline stem cells express SSEA1. However, in addition to its status as a classical, murine stem cell marker, SSEA-1 is a haematopoietic differentiation antigen expressed on most terminally differentiated myeloid cells.
Crucially, the identification of oocytes from co-expression of germ-cell markers with EGFP immunofluorescence in experiments using the TgOG2 mouse [12, 13] rests on the exclusivity of expression of Oct4-EGFP in the germline. However, Yoshimizu et al.  reported that in TgOG2 transgenic embryos, EGFP expression is not entirely germ-cell specific, with "faint but significant expression" throughout the epiblast. (This observation was analysed further and attributed to the presence of residual elements in the epiblast-specific enhancer .) Moreover, the original analysis of tissue-specific expression in adult TgOG2 mice  was not exhaustive. It is relevant that expression of Oct4 has been reported in adult stem cell populations and tumours [58, 92], human diseased arteries , and rabbit atherosclerotic plaques , by unknown regulatory mechanisms. The hypoxia-inducible factor, HIF-2α, has been shown to bind directly to the Oct4 promoter and enhancer regions, activating the gene and eliciting a tumorigenic activity . Therefore, can Oct4 transcription from the distal enhancer be considered as absolutely germ-cell specific? A factor present in Xenopus oocytes, tumour-associated factor or Tpt1, activates Oct4 transcription in mouse somatic-cell and ES-cell nuclei by binding to the Oct4 gene sequence directly - effectively bypassing the promoter and enhancer elements . Tpt1 is expressed by macrophages resident in the testes of neonatal and adult male rats, and in adult human testis . Therefore, it is suggested that macrophages have the inherent capacity, through expression of Tpt1, to transcribe embryonic forms of Oct4.
Lee et al.  derived mononuclear cells from peripheral blood of TgOG2 female mice, and were unable to detect EGFP+ cells in the CD45+ fraction. Therefore it is inferred here that Oct4-EGFP expression may occur in macrophages, but not the circulating monocytes from which the tissue macrophages derive. Expression of Oct4 by the macrophage has been reported, in atherosclerotic plaques of rabbits .
(b) Potential involvement of the macrophage
A further reason to implicate the macrophage in the structures identified as de novo oocytes [12, 13] arises from the various functions it performs in the ovary . The macrophage has been documented within atretic follicles , where it clears apoptotic granulosa cells. In the foetal pig ovary, macrophages have been observed to phagocytise degenerating oogonia and oocytes, the nuclei being clearly visible in the macrophage cytoplasm . Pepling and Spradling  have shown that apoptotic oogonia still demonstrate Mvh antigenicity. Therefore, could some designated oocytes (e.g. Figure seven 'M'-'O' in Johnson et al. ) that co-express oocyte markers and EGFP consist of macrophages performing phagocytosis of an oocyte? The phenomenon interpreted as de novo oocytes [12, 13, 15] therefore might be explained by macrophage clearance of degenerating and/or apoptotic oocytes following ovotoxic treatment, by phagocytosis and antigen processing. This hypothesis predicts that the structures in question would arise more rarely during homeostasis and parabiosis than following ovotoxic treatment; and that the timing of detection is crucial, the clearance of degenerating oocytes occurring over weeks. This may explain why EGFP-labelled structures can be detected within 30 h of transplantation , and yet show variable detection after 2 months (Eggan et al.  versus Lee et al. ). There emerges a need for in situ analysis using markers for immune cells, as advocated by Eggan et al. , in order to test these possibilities.
(c) De novo oocytes as potential artefacts
Johnson et al.  transplanted peripheral blood cells from Oct4-EGFP-carrying TgOG2 mice to CT-treated wt and Atm-/- female mice, to establish migration of blood-borne oocyte precursors to the depleted ovary. The authors presented photomicrographs (Figure seven, 'A'-'R') in which presumptive de novo oocytes in non-follicular structures stain positively by immunofluorescence for EGFP and germ-cell markers. However, the aspect of images 'A'-'L' and 'P'-'R' resembles autofluorescence - indeed, the artefact was indicated by the authors in neighbouring cells in Figure seven, 'P'-'R'. Autofluorescent cells include macrophages, dendritic cells, lymphocytes and granulocytes. The designated oocytes in Figure seven, 'A'-'L' and 'P'-'R', resemble dendritic cells, which are highly fluorescent and emit within the wavelength spectrum of the fluorochromes, fluorescein, isothiocyanate and phycoerythrin . Autofluorescence has been reported previously for luteal cells of the macaque , and stromal tissues of the rat ovary .
(d) Distinct temporal and spatial niches for germ cell and haematopoietic lineage specification
Finally, in considering a possible supply of extra-ovarian germ cell precursors, Johnson et al.  reasoned that the bone marrow would be a logical source, due to a stated similarity in location and timing of embryonic haematopoietic induction and PGC specification. As with the PGC, segregation of the haemangioblast, the precursor of haematopoietic and endothelial lineages, occurs in a temporally and spatially defined manner. It is a mesodermal derivative of transient existence, arising within the length of the posterior primitive streak during a 12-18 h window, from midgastrulation (E7) to head-fold stages. Haemangioblasts differentiate rapidly on emigration from this origin  towards two sites: the yolk sac, for the primitive erythroid lineage, and endothelial and vascular smooth muscle progenitors; and the para-aortic splanchnopleura, for lymphoid progenitors and HSC. Therefore, the PGC and haemangioblast differ in their site of emergence (base of the allantois, versus a more distal location in the posterior primitive streak, respectively), and in their immediate progenitors (proximal and posterior epiblast, versus mesoderm). The exact location of PGC and of haemangioblast derivatives within the extraembryonic tissues also differs (base of the within extraembryonic mesoderm, versus on the yolk sac surface facing the exocoelomic cavity, respectively, by E7.5). Furthermore, ectopic PGC have only been observed in the mesonephric tissue, where they undergo meiotic arrest . No PGC have ever been noted in the circulation of mammals . Moreover, the gene expression profile of germ cells from precursor stages to PGC specification is lineage specific, with sequential induction Blimp1 , Fragilis and Stella , and down regulation of somatically expressed genes. Therefore there is no evidence for a separate or branching germline during gastrulation.
It should also be emphasised that to date, no definitive evidence exists that those oocytes that are recruited for maturation and fertilisation in vivo originate from any other source than the classical germline. Furthermore, the ovary remains the exclusive site of regulation of meiosis and oocyte maturation.
(v) Functional, female germline stem cells
Another challenge to the concept of a fixed ovarian pool at birth was made by Zou et al. , who claimed to have isolated female germline stem cell (FGSC) lines from both neonatal and adult mice ovaries (the adult mice being of unspecified age), having first identified putative FGSC in the OSE of neonatal and adult mice by BrdU-incorporation (see section (i), above). Remarkably, FGSC lines were shown to be capable of reassembly into follicles on reintroduction into a sterile ovary, and produced viable offspring that transmitted a transgene through the germline. The authors take their considerable achievements as validating the existence of a germline stem cell population in the ovary, but do not consider the possibility that their lines arise from quiescent oogonia present in the postnatal ovary, which are induced to proliferate in culture under conditions devised originally to be highly mitogenic for SSC (Figure 1). Arguments leading to this conclusion are presented below. A starting premise is the existence of oogonia in the postnatal mouse ovary, as documented previously by Pepling and Spradling , and Greenbaum et al. : about 10% of germ cells persist within small germline cysts containing 2-4 cells at 26.5 d.p.c., or day 7 postnatal .
(a) Constituent phenotypes of explanted germ cells include oogonia
A relatively straightforward procedure was used by Zou et al.  to isolate FGSC lines: cell suspensions were prepared from whole ovaries, and a very few cells (approximately 10 per mouse) were isolated by immunomagnetic separation using anti-Mvh antibody. Although the location of Mvh is usually considered to be cytoplasmic in PGC, oogonia and oocytes , the stated rationale for this separation was based on the presence of purported trans-membrane sequences in the Mvh protein . The validity of these sequence assignations was questioned by Abban and Johnson , who emphasised the need for further analysis of FGSC surface immunogenicity. It may be relevant, in this connection, that specific Fc receptors, Fcγ RI, II, III, are present on oocytes [110–112], and an IgG-binding antigen has been demonstrated in SSC . Therefore the possibility arises that in the study of Zou et al. , cell isolation resulted from an artefact of the antibody coated microbeads binding via their Fc moieties to the Fc receptors  on the oolemma, if not also on the plasma membrane of the oogonia, the female counterparts of SSC (which theme is developed below). According to conventional theory , the purified, Mvh-expressing germ cells should consist entirely of (ZP-free) primary oocytes and oogonia, without contribution from any distinct population of germline stem cells.
(b) The morphology of FGSC lines resembles that of cultured oogonia
In the system of Zou et al. , cells proliferated in a feeder-based culture system formulated initially for SSC expansion, containing LIF, putrescine, EGF, GDNF, bFGF, insulin and transferrin. The proliferating cells that resulted were described as forming compact clusters and having blurred cell boundaries - these are characteristic features of oogonia proliferating in ovarian germline cysts , as well as proliferating SSC . The morphology of FGSC in culture also resembles that of cultured oogonia (which in some earlier publications are referred to as mitotic PGC having reached the non-motile phase) [115–119]: namely, rounded cells with large nuclei and without lamellipodia, with moderate alkaline phosphatase staining, and non-adherent to the substratum. In culture, the (earlier, migratory phase) PGC proper transform with time into cells having this morphology .
Previously the long-term culture of oogonia was problematical. The inability to extend the culture period substantially was attributed to the cell-autonomous behaviour of PGC and their derivatives, causing growth arrest as well as morphological changes. Kawase et al.  and Nakatsuji et al.  prolonged proliferation to a limited degree by specific culture conditions or suppression of apoptosis, respectively.
(e) Cultured oogonia undergo development and ovulation in vivo
Previous studies have demonstrated the ability of cultured oogonia to assemble into follicles when recombined with ovarian somatic cells [66, 119], and to produce live offspring on transplantation into partially ovariectomised mice .
(f) The gene expression profile of FGSC resembles that of growth-arrested oogonia
Zou et al.  noted that their FGSC lines are dissimilar to ES cells in their gene expression pattern: FGSC expressed Oct4, MVH, Dazl, Blimp-1, Fragilis, Stella and Rex-1; but not c-kit, Figla (a marker for primordial follicle formation), Sox-2, Nanog, Scp1-3 or ZP3. The combined expression of Oct4, Sox-2 and Nanog, the regulatory network of genes for maintaining multipotency, is considered prerequisite to a self-renewing stem cell population, not only in embryonic but also in adult systems  (see also section 2.(ii)). Therefore, the FGSC expression pattern is inconsistent with a stem-cell phenotype, specifically mouse EG cells and mouse PGC, which are Sox2+, Nanog+, c-kit+ . However, the gene expression profile of FGSC (Oct4+, MVH+, Dazl+, Blimp-1+, Fragilis+, Stella+ and Rex-1+; c-kit-, Figla-, Sox-2-, Nanog-, Scp1-3- and ZP3-) is more consistent with oogonia [3, 41, 64, 65, 120] except for one notable feature - a lack of c-kit expression. During development of male and female mouse germ cells, c-kit expression ceases coincident with entry into the non-proliferative phase, between 13.5 and 15.5 d.p.c. [121, 122]; and c-kit expression is absent from oogonia at 15.5 d.p.c. . Therefore the possibility arises that the founding population of cells giving rise to the FGSC lines of Zou et al.  are growth-arrested oogonia, proposed to reside within those residual, small cysts of the neonatal mouse ovary [33, 109]. Oogonia, like FGSC, are diploid and carry erased, gynogenetic imprints [3, 120].
(g) Functional parallels between FGSC and SSC
It is significant that the culture medium used to derive the FGSC lines was used initially for the derivation of SSC lines . In the adult mouse testis, c-kit is expressed by differentiating spermatogonia, but not by undifferentiated, testis repopulating SSC [63, 81]. C-kit expression was analysed in the first SSC lines to be isolated , and found to be absent from undifferentiated, proliferating SSC and confined to differentiating derivatives.
Therefore, the capacity of oogonia to proliferate (without resumption of c-kit expression) in medium optimised for SSC would provide an additional example of the sex-independent properties of male and female germ cells up to the stage of growth arrest [122, 124]. To paraphrase Baltus et al. , premeiotic DNA replication is a terminal differentiating event in the oogonium as a sexually undifferentiated precursor cell. By extrapolation of this insight, the premeiotic oogonia in the postnatal ovary have not yet undergone the differentiation process, and may be prone to resume mitosis provided that specific culture requirements are met. This hypothesis is developed in the legend to Figure 1.
(g) Implications of lack of c-kit expression by FGSC and oogonia
A predicted consequence of the lack of c-kit expression by FGSC of Zou et al.  is resistance to the effects of BU (as in SSC, see section (iii)). Therefore, BU administration should not eliminate this purported stem-cell population in vivo and oogenesis should resume with time, as is observed for spermatogenesis in the BU-treated male mouse . However as noted in section (iii), the converse is observed as BU treatment leads to extinction of female fertility [7, 80]. This provides circumstantial evidence against FGSC acting as facultative stem cells to support neo- oogenesis in vivo, either during homeostasis or following ovotoxic damage. By the same rationale, the lack of c-kit expression by growth-arrested oogonia [121–123] argues against their status as functional stem cell progenitors of ooyctes in vivo.
Nevertheless it is of interest to establish the size and cell cycle status of the oogonial population in the post-natal ovary. However, persistence of mitotic oogonia in the adult mouse is difficult to reconcile with the absence of detectable SSEA-1 in germ cells of the adult ovary , because oogonia proliferating in vivo are positive for this marker . In the human, clusters of residual oogonia have been noted in late foetal ovaries but never in adult ovaries; and were thought to arise from errors in follicular development, and to be destined for elimination . That the same fate (apoptosis, extrusion) applies ultimately to those residual, growth-arrested oogonia in the neonatal mouse ovary is favoured here.
3. Neo-oogenesis versus classical theory: accounting for fertility preservation, post CT-induced ovarian failure, by BMT
So far, alternative explanations have been presented for main observations advanced in support of neo- oogenesis, leading to the proposition that the hypothesis is erroneous and may lead to false directions for the preservation of female fertility. This is illustrated by a significant observation made by Johnson et al.  and Lee et al.  in adult female mice subjected to ovotoxic CT: BMT to these mice resulted in restoration of follicle production, compared with continued sterility in CT-treated mice not receiving BMT. Johnson et al.  and Lee et al.  regard this observation as validating their contention that a reservoir of germline stem cells exists in the bone marrow, so that BMT reinstates host neo- oogenesis by delivery of oocyte precursors. However, the observation of Johnson et al.  and Lee et al.  may be interpreted differently, in accordance with a fixed oocyte reserve . This alternative explanation draws on currently proposed mechanisms of autoimmune ovarian failure to suggest a protective effect of BMT on resident oocytes, which possibility previously was discounted .
A series of events is posited to occur during the experimental manipulations [12, 13], illustrated in Figure 2: (A) maintenance of self-tolerance to ovarian antigens during homeostasis; (B) after ovotoxic CT, induction of apoptosis in follicular cells leading to failure of tolerance, induction of autoimmunity against ovarian antigens, and subsequent destruction of surviving follicles; and (C) after BMT and establishment of haematopoietic chimaerism, restoration of tolerance and resumption of development of surviving follicles. Evidence for these events is now considered in detail.
(A) Self tolerance in the steady state ovary
It has been amply demonstrated in mouse models that during homeostasis there predominates self-tolerance to ovarian antigens, sustained by a mechanism dependent specifically on regulatory T cells (Treg). (Treg, either thymus derived or produced by activation of naïve T cells, function to suppress activation of T, B and NK cells.) In the steady-state ovary, atretic follicles contain degenerating ooyctes that are the targets of autoreactive CD4+ T cells . Concurrently, ovarian antigens continuously stimulate Treg in the regional lymph nodes to maintain self-tolerance [127, 128]. Autoimmune ovarian disease (AOD) results from loss of functional Treg, e.g. by thymectomy or iatrogenic effects, so that self-tolerance is converted into an active T cell response [128–130]. In their study of AOD in the thymectomised mouse model, Wheeler et al.  further demonstrated that ovarian antigen-specific Treg are capacitated by autoantigen exposure within regional, draining lymph nodes; and that AOD development can be abrogated in the thymectomised recipients by transfer of Treg from the lymph nodes of normal female donors. This Treg-based mechanism may be directly relevant to the studies under consideration here [12, 13].
(B) Effects of CT treatment - induction of autoimmunity
The CT combination of cyclophosphamide (CY) and BU causes catastrophic damage to oocytes and ovarian failure [12, 13], and is likely to increase apoptosis, which functions normally to promote oocyte clearance and tissue remodelling. According to current thinking, efficient apoptosis provides a safeguard against autoimmunity. But a high burden of apoptosis is strongly implicated in the development of the autoimmune state, by cellular spillage or increased exposure of the immune system to autoantigens . By this reasoning, CT would serve as a trigger for autoimmunity in the ovary, whereby the load of apoptotic cells may exceed the clearance capacity of macrophages and/or dendritic cells.
Cyclophosphamide (CY), the chemotherapeutic alkylating agent used in combination with BU as an ovotoxic agent [12, 13], constitutes possibly an additional trigger for autoimmunity. CY has established immune-enhancing effects, involving both the stimulatory and suppressive arms of adaptive immunity: CY treatment augments effector T-cell stimulation, while selectively depleting Treg numbers and function . These actions of CY are achieved by alteration of subsets of dendritic cells in lymphoid tissue, which normally maintain peripheral tolerance via Treg activation .
In a highly relevant study that used the non-obese diabetic (NOD) mouse model, Brode et al.  demonstrated the potential of Treg to abrogate organ-specific autoimmunity, and deduced the existence of a temporal window between disease induction and development of an autoreactive T cell response during which suppression would be effective. A single injection of CY induced onset of the autoimmune syndrome, type 1 diabetes (T1D), which was synchronous with selective reduction in Treg in lymph nodes through apoptosis, and with reduced suppressive capacity of Treg in vitro. Furthermore, the ensuing autoreactive T cell response could be suppressed, and development of T1D abrogated, by transfer of antigen-specific Treg from a non-diabetic, syngeneic donor to CY-treated, NOD recipients - provided that Treg were received between 1 and 8 d after CY treatment. Thereafter, the developing autoreactive T cell response predominated. A mechanism was proposed for the action of CY, whereby an imbalance created between CD4+CD25- T cells and Treg leads to priming of autoreactive T cells and development of autoimmunity. (Normally, interaction of Treg with dendritic cells within lymph nodes suppresses the priming of naïve autoreactive T cells.)
A mechanism is therefore proposed from (A) and (B) for the studies considered [12, 13], by which CT treatment induced ovarian failure and apoptosis, and caused depletion of ovarian antigen-specific Treg, thereby promoting activation of effector T cells and inducing autoimmunity to ovarian antigens. A proportion of oocytes may have survived, but a switch from self-tolerance to intolerance caused these to be eventually cleared. It is in keeping with this hypothesis that autoimmune premature ovarian failure in humans is characterised by inflammatory infiltration into developing follicles and the production of anti-ovarian autoantibodies, while primordial follicles are spared [134–136]. Also, immunosuppressive, corticosteroid therapy may lead to resumption of menses in women with autoimmune oophoritis with secondary amenorrhea .
(C) Restoration of tolerance
In mouse models, reconstitution of the immuno-haematopoietic system by BMT or transfer of HSC attenuates autoimmunity and may achieve disease remission (reviewed by Kaminitz et al. ). The mechanism of such modulation may involve resetting immune homeostasis [138–140] or reversal of spontaneous autoimmunity, for example by clonal deletion, anergy, or suppression [137, 141]. In the proposed scenario of the ovary with developing autoimmunity to ovarian antigens following CT (A, B), immuno-modulation would be restored by the haematopoietic chimaerism induced by syngeneic BMT, with resumption of self-tolerance. And it is suggested that the specific tolerogenic mechanism would involve restoration of suppressive Treg function by BMT, either from donor stem cells developing in the recipient's thymus, or from bone marrow acting as a natural reservoir for homeostatic trafficking of functional, activated Treg . The transient immunosuppressive and lymphopenic effect of CY , given in combination with BU as ovotoxic treatment, also would provide a niche for homeostatic expansion of Treg following BMT . Consequently, remaining primordial follicles would grow and reach ovulation, rather than be cleared as in control, CT-treated mice not receiving BMT.
Returning to the study of Lee et al. , several observations can now be reinterpreted:
(i) Beneficial effects on fertility are attenuated when BMT is postponed from 1 week to 2 months following CT. This can be explained by the priming of an autoreactive T cell response after 1 week, in accord with Brode et al.  (see (B), above). BMT at 2 months is ineffective, and there is progressive destruction of the surviving oocyte reserve by immune clearance.
(ii) Postponement of mating after CT and BMT by two months versus 1 week results in decreased fertility. This can be explained by exhaustion of the surviving oocyte reserve in the 2-month interim period by oestrus cycling (occurring every 3-5 days), compared with the suspension of oestrus cycling during consecutive pregnancies.
This line of reasoning also may account for the observations of Johnson et al.  with Atm-/- mice. Although ovaries of mutant females are described as devoid of oocytes and developing follicles , evidence exists for the persistence of residual germ cells: rare and abnormal oocytes were recorded in Atm-/- mice that were 20 days old , and between 17 and 29 days old . This accords with the observation of Johnson et al.  of low-level, germ cell-specific gene expression (Oct4, Mvh, Dazl and Stella) in ovaries from adult Atm-/- mice. Crucially, Johnson et al.  noted that, following ovotoxic CT and BMT, ovaries from Atm-/- mice contained a small number (maximum, 25) of follicles at 2 and 11.5 months after BMT, while non-transplanted mice did not. It is suggested here that ovarian failure caused by Atm-deficiency also may induce autoimmunity to ovarian antigens, resulting in clearance of those rare, residual oocytes. Thus, BMT to Atm-/- mice would restore tolerance, allowing those surviving oocytes to develop to antral stages .
This hypothesis of CT-induced autoimmunity and its suppression by immune-cell transfer gives a prediction for the system of Eggan et al. , where female mice were subjected to CT (with BU and CY) and 1 d later were connected parabiotically to untreated partners, to provide a shared circulatory system. In this case, the priming of an ovarian autoreactive T cell response in the CT-treated mouse would be suppressed by functional, ovarian antigen-specific Treg transfusing from the untreated partner, thereby imposing a state of dominant self-tolerance in both parabionts (Figure 2D). That Eggan et al.  found no evidence for restoration of fertility in the CT-treated mice by parabiosis, nor in CT-treated (non-parabiotic) mice by BMT, most likely reflects their use of superovulation as the measure of ovarian function. (The technique was used primarily to harvest large numbers of oocytes, to ascertain any contribution of blood-derived precursors to neo- oogenesis.) However, there is inherent variance in the superovulatory response in mice (which is apparent in the data presented), and a dependence of superovulation on the instantaneous number of hormonally responsive, antral follicles. Consequently, the superovulated yield would not reflect the size of the primordial and growing follicle pool - especially when these are close to exhaustion following CT. Therefore, superovulation would not provide an accurate indicator of long-term fertility. The measures taken by Johnson et al.  and Lee et al.  to assess fertility are more effective, analysing total numbers of non-atretic immature follicles per ovary, and recording live-birth pregnancies over time, respectively.
To paraphrase Oktay and Oktem , further investigation is needed into the mechanism of rescue of fertility in CT treated females by BMT. Establishing the validity or otherwise of the neo- oogenesis concept is crucial to understanding germinal function, and to preserving fertility. The proposed involvement of the immune system may, on the other hand, offer possibilities for preserving ovarian function in women undergoing CT, and for treatment of AOD and primary ovarian insufficiency, e.g. by Treg-based immunotherapy .
In summary, re-examination of experimental findings cited by proponents of neo- oogenesis in mammals as validating their hypothesis leads to alternative interpretations drawn from published literature, which are entirely consistent with the long-standing orthodoxy of a determinate oocyte reserve . By comparing those studies collectively advocating neo- oogenesis, recurrent themes emerge.
Firstly, several studies used as starting material ovaries from mice either termed 'juvenile'  or specified as day 5  or days 2-5 postnatal , to locate mitotic germline stem cells within the OSE. This may represent an injudicious choice as the neonatal period between birth and day 5 postnatal is one of flux for mouse ovarian germ cells: at this time, ovarian cyst breakdown occurs concomitantly with a high rate of oocyte attrition, while meiotic progression continues in other oocytes towards diplotene with formation of primordial follicles . That the majority of oocytes attain diplotene only by day 5 postnatal signifies that meiotic DNA recombination and repair may still be ongoing in tardy oocytes, which phenomenon is argued to underlie the observation of BrdU incorporation into germ cells, as well as apparent mtDNA synthesis (section 2.(i)). (Regarding BrdU incorporation by germ cells in adult ovaries , the precise extent of DNA recombination/repair in oocytes at later stages is unknown.) Added to this, oocytes that are defective or delayed may be actively extruded from the OSE  (and see section 2.(i)). In short, the aforementioned studies involving in situ anti-BrdU immunocytochemical analyses of germ cells at the surface of the neonatal ovary [7, 10, 11] may have captured these dynamic processes, rather than mitotic replication of germline stem cells. Crucially, in the neonatal ovary a significant proportion (~10%) of germ cells persist in germline cysts , which are posited here to provide the founding cell type for the FGSC lines of Zou et al. , and to be a likely component of the cultures produced by Pacchiarotti et al. . The potential involvement of oogonia in those cultures of putative germline stem cells is a second recurring theme.
A third theme is misidentification of somatic cell types as germ cells (section 2.(ii)). It is inferred that cultures of putative germline stem cells derived from mouse ovaries [8, 9, 11] were confounded by the presence of somatic cells, from cell morphology and gene expression patterns. In some cases cell lines were identifiable as regenerative ovarian epithelium [9, 11]. This cautions against reliance on presumed germ-cell specificity of markers for stem-cell validation, and emphasises the need for recognition of OSE as a complex and multipotent tissue . Concerns for cellular misidentification extend also to immune cells of the ovary, and specifically macrophages, which are suggested instead to constitute those structures described as de novo oocytes provided by blood-borne precursors [12, 13, 15].
A fourth emerging theme is that detailed consideration of the c-kit/SCF signaling pathway in germ cells, in the light of data presented [7, 10], countermands the existence of neo-oogenesis and female germline stem cells. Much has been made of the sterilising effects of BU treatment in female mice as proving the existence of germline stem cells in the ovary [7, 12, 15]; but section 2.(iii) provides arguments directly contradicting statements by Tilly et al.  that BU targets only replicative stem cells, and not primordial or later follicles. Data from spermatogenic and haematopoietic systems, where the respective stem cells are refractory to the effects of this agent, indicate that abrogation of c-kit function is central to its mechanism of toxicity . This both predicts and explains the observed, devastating effects of BU on folliculogenesis, from primordial to later stages, where both germ and somatic cells depend on functional c-kit/SCF signaling for survival. Observations that BU dosages causing transient myelosuppression  produce irreversible sterility in female mice [7, 80] are therefore consistent with a fixed oocyte reserve, without a stem cell compartment, and without replenishment from bone marrow-derived precursors. Furthermore, the proliferating FGSC of Zou et al.  lack c-kit expression, and therefore would be refractory to BU treatment in vivo. That fertility is not restored with time following BU treatment in female mice [7, 80], as it is in male mice [81, 82], argues against this population occupying a facultative stem cell niche in vivo, as was proposed previously [25, 26].
The FGSC lines of Zou et al.  were equated to cultures of oogonia, from cell morphology, patterns of gene expression, functionality as oocyte precursors following transplantation to ovaries, and by comparison with previous studies. This cell type may further reinforce the functional equivalence of premeiotic male and female germ cells [124, 147]; in this case with respect to growth requirements for proliferation in culture, as conditions for FGSC culture were optimised previously for SSC [10, 148]. Historically, efforts were directed towards isolation of EG cells from PGC, which transformation can be achieved in germ cells isolated up to day 12.5 p.c. . Therefore, the experimental utility of oogonia, so well exemplified by the work of Zou et al. , may have been overlooked in the pursuit of EG cells, until now.
Finally, an explanation was offered for the observed restoration of fertility in CT treated mice by BMT that is entirely in keeping with the orthodox theory of a fixed oocyte reserve , rather than neo-oogenesis: i.e., by regulation of autoimmunity, and not by the supply of blood-borne oocyte precursors. The clinical importance of conserving fertility in women undergoing CT gives urgency to the resolution of this ongoing controversy.
autoimmune ovarian disease
bone marrow transplantation
enhanced green fluorescent protein
embryonic germ (cell)
embryonic stem (cell)
female germline stem cells
haematopoietic stem cells
mouse VASA homologue
ovarian surface epithelium
peripheral blood cell transplantation
primordial germ cell
spermatogonial stem cells
type 1 diabetes
Zuckerman S: The number of oocytes in the mature ovary. Recent Prog Horm Res 1951, 6: 63–108.
McLaren A: Germ and somatic cell lineages in the developing gonad. Mol Cell Endocrinol 2000, 163: 3–9. 10.1016/S0303-7207(99)00234-8
McLaren A: Primordial germ cells in the mouse. Developmental Biology 2003, 262: 1–15. 10.1016/S0012-1606(03)00214-8
Cohen AA: Female post-reproductive lifespan: a general mammalian trait. Biol Rev 2004, 79: 733–750. 10.1017/S1464793103006432
Broekmans FJ, Soules MR, Fauser BC: Ovarian aging: mechanism and clinical consequences. Endocr Rev 2009, 30: 465–493. 10.1210/er.2009-0006
Miao Y-L, Kikuchi K, Sun Q-Y, Schatten H: Oocyte aging: cellular and molecular changes, developmental potential and reversal possibility. Hum Reprod Update 2009, 1: 1–13.
Johnson J, Canning J, Kaneko T, Pru JK, Tilly JL: Germline stem cells and follicular renewal in the postnatal mammalian ovary. Nature 2004, 428: 145–50. 10.1038/nature02316
Bukovsky A, Svetlikova M, Caudle MR: Oogenesis in cultures derived from adult human ovaries. Reprod Biol Endocrinol 3: 17. 10.1186/1477-7827-3-17
Virant-Klun I, Rožman P, Cvjeticanin B, Vracnik-Bokal E, Novakovic S, Rülicke T, Dovc P, Meden-Vrtovec H: Parthenogenetic embryo-like structures in the human ovarian surface epithelium cell culture in postmenopausal women with no naturally present follicles and oocytes. Stem Cells Dev 2009, 18: 137–149. 10.1089/scd.2007.0238
Zou K, Yuan Z, Yang Z, Luo H, Sun K, Zhou L, Xiang J, Shi L, Yu Q, Zhang Y, Hou R, Wu J: Production of offspring from a germline stem cell line derived from neonatal ovaries. Nature Cell Biol 2009, 11: 631–636. 10.1038/ncb1869
Pacchiarotti J, Maki C, Ramos T, Marh J, Howerton K, Wong J, Pham J, Anorve S, Chow Y-C, Izadyar F: Differentiation potential of germ line stem cells derived from the postnatal mouse ovary. Differentiation 2010, 79: 159–170. 10.1016/j.diff.2010.01.001
Johnson J, Bagley J, Skaznik-Wikiel M, Lee HJ, Admas GB, Niikura Y, Tschudy KS, Tilly JC, Cortes ML, Forkert R, Spitzer T, Iacomini J, Scadden DT, Tilly J: Oocyte generation in adult mammalian ovaries by putative germ cells derived from bone marrow and peripheral blood. Cell 2005, 122: 303–15. 10.1016/j.cell.2005.06.031
Lee HJ, Selesniemi K, Niikura Y, Klein R, Dombkowski DM, Tilly JL: Bone marrow transplantation generates immature oocytes and rescues longterm fertility in a preclinical mouse model of chemotherapy induced premature ovarian failure. J Clin Oncol 2007, 25: 3198–3204. 10.1200/JCO.2006.10.3028
Eggan K, Jurga S, Gosden R, Min IM, Wagers AJ: Ovulated oocytes in adult mice derive from non-circulating germ cells. Nature 2006, 441: 1109–1114. 10.1038/nature04929
Tilly JL, Niikura Y, Rueda BR: The current status of evidence for and against postnatal oogenesis in mammals: a case of ovarian optimism versus pessimism? Biol Reprod 2009, 80: 2–12. 10.1095/biolreprod.108.069088
Abban G, Johnson J: Stem cell support of oogenesis in the human. Human Reprod 2009, 24: 2974–2978. 10.1093/humrep/dep281
Bristol-Gould SK, Kreeger PK, Selkirk CG, Kilen SM, Mayo KE, Shea LD, Woodruff TK: Fate of the initial follicle pool: empirical and mathematical evidence supporting its sufficiency for adult fertility. Dev Biol 2006, 298: 149–154. 10.1016/j.ydbio.2006.06.023
Faddy M, Gosden R: Let's not ignore the statistics. Biol Reprod 2009, 81: 231–232. 10.1095/biolreprod.109.078287
Wallace WHB, Kelsey TW: Human ovarian reserve from conception to the menopause. PLoS One 2010, 5: e8772. 10.1371/journal.pone.0008772
Tilly JL, Johnson J: Recent arguments against germ cell renewal in the adult human ovary: Is an absence of marker gene expression really acceptable evidence of an absence of oogenesis? Cell Cycle 2007, 8: 879–883.
Byskov AG, Faddy MJ, Lemmen JG, Andersen CY: Eggs forever? Differentiation 2005, 73: 438–446. 10.1111/j.1432-0436.2005.00045.x
Telfer EE, Gosden RG, Byskov AG, Spears N, Albertini D, Anderson CY, Anderson R, Braw-Tal R, Clarke H, Gougeon A, McLaughlin E, McLaren A, McNatty K, Schatten G, Silber S, Tsafriri A: On regenerating the ovary and generating controversy. Cell 2005, 122: 821–822. 10.1016/j.cell.2005.09.004
Begum S, Papaioannou VE, Gosden RG: The oocyte population is not renewed in transplanted or irradiated adult ovaries. Human Reprod 2008, 23: 2326–2330. 10.1093/humrep/den249
Gosden R, Telfer E, Faddy M: Germ line stem cells and adult ovarian function. In Stem Cells and Human Reproduction. Edited by: Simon C, Pellicer A. London: Informa Healthcare; 2009:58–69.
Tilly JL, Telfer E: Purification of germline stem cells from adult mammalian ovaries: a step closer towards control of the female biological clock? Mol Hum Reprod 2009, 15: 393–398. 10.1093/molehr/gap036
De Felici M: Germ stem cells in the mammalian adult ovary: considerations by a fan of the primordial germ cells. Mol Hum Reprod 2010, 16: 632–636. 10.1093/molehr/gaq006
Bogenhagen D, Clayton DA: The number of mitochondrial deoxyribonucleic acid genomes in mouse L and human HeLa cells. J Biol Chem 1974, 249: 7991–7995.
Davis AF, Clayton DA: In situ localization of mtDNA replication in intact mammalian cells. J Cell Biol 1996, 135: 883–893. 10.1083/jcb.135.4.883
Attardi B, Attardi G: Persistence of thymidine kinase activity in mitochondria of a thymidine-kinase-deficient derivative of mouse L cells. P Natl Acad Sci USA 1972, 69: 2874–2878. 10.1073/pnas.69.10.2874
Berk A, Clayton DA: A genetically distinct thymidine kinase in mammalian mitochondria. J Biol Chem 1973, 248: 2722–2729.
Jansen RP, de Boer K: The bottleneck: mitochondrial imperatives in oogenesis and ovarian follicular fate. Mol Cell Endocrinol 1998, 145: 81–88. 10.1016/S0303-7207(98)00173-7
Piko L, Matsumoto L: Number of mitochondria and some properties of mitochondrial DNA in the mouse egg. Dev Biol 1976, 49: 1–10. 10.1016/0012-1606(76)90253-0
Pepling ME, Spradling AC: Mouse ovarian germ cell cysts undergo programmed breakdown to form primordial follicles. Dev Biol 2001, 234: 339–351. 10.1006/dbio.2001.0269
Tourte M, Mignotte F, Mounolou JC: Heterogeneous distribution and replication activity of mitochondria in Xenopus laevis oocytes. Eur J Cell Biol 1984, 34: 171–178.
Rubbi CP, Milner J: Analysis of nucleotide excision repair by detection of single-stranded DNA transients. Carcinogenesis 2001, 22: 1789–1796. 10.1093/carcin/22.11.1789
Smith A, Haaf T: DNA nicks and increased sensitivity of DNA to fluorescence in situ end labeling during functional spermiogenesis. BioTechniques 1998, 25: 496–502.
Menézo Y Jr, Russo G-L, Tosti E, El Mouatassim S, Benkhalifa M: Expression profile of genes coding for DNA repair in human oocytes using pangenomic microarrays, with a special focus on ROS linked decays. J Assist Reprod Gen 2007, 4: 513–520.
Oktay K, Schenken RS, Nelson JF: Proliferating cell nuclear antigen marks the initiation of follicular growth in the rat. Biol Reprod 1995, 53: 295–301. 10.1095/biolreprod53.2.295
Wang H, Höög C: Structural damage to meiotic chromosomes impairs DNA recombination and checkpoint control in mammalian oocytes. J Cell Biol 2007, 173: 485–495. 10.1083/jcb.200512077
Ghafari F, Gutierrez CG, Hartshorne G: Apoptosis in mouse fetal and neonatal mouse ovaries during meiotic prophase one. BioMed Central Dev Biol 2007, 7: 87.
Pepling ME: From primordial germ cell to primordial follicle: mammalian female germ cell development. Genesis 2006, 44: 622–632. 10.1002/dvg.20258
Butler H, Juma MB: Oogenesis in an adult prosimian. Nature 1970, 226: 552–553. 10.1038/226552a0
David GFX, Kumar TCA, Baker TG: Uptake of tritiated thymidine by primordial germinal cells in the ovaries of the adult slender loris. J Reprod Fert 1974, 41: 447–451. 10.1530/jrf.0.0410447
Crone M, Peters H: Unusual incorporation of tritiated thymidine into early diplotene oocytes of mice. Exp Cell Res 1968, 50: 664–668. 10.1016/0014-4827(68)90432-1
Motta PM, Makabem S, Nottola S: The ultrastructure of human reproduction. I. The natural history of the female germ cell: origin, migration and differentiation inside the developing ovary. Hum Reprod Update 1997, 3: 281–295. 10.1093/humupd/3.3.281
Fink SL, Cookson BT: Apoptosis, pyrosis and necrosis: mechanistic description of dead and dying eukaryotic cells. Infect Immun 2005, 73: 1907–1916. 10.1128/IAI.73.4.1907-1916.2005
Puhlev I, Guo N, Brown DR, Levine F: Desiccation tolerance in human cells. Cryobiology 2001, 42: 207–217. 10.1006/cryo.2001.2324
Garcia de Castro A, Tunnacliffe A: Intracellular trehalose improves osmotolerance but not desiccation in mammalian cells. FEBS Lett 2000, 487: 199–202. 10.1016/S0014-5793(00)02340-1
Huang Z, Tunnacliffe A: Gene induction by desiccation stress in human cell cultures. FEBS Lett 2005, 579: 4973–4977. 10.1016/j.febslet.2005.07.084
Skinner SM, Dunbar BS: Localization of a carbohydrate antigen associated with growing oocytes and ovarian surface epithelium. J Histochem Cytochem 1992, 40: 1030–1036.
Parrott JA, Mosher R, Kim G, Skinner MK: Autocrine interactions of keratinocyte growth factor, hepatocyte growth factor, and kit-ligand in the regulation of normal ovarian surface epithelial cells. Endocrinology 2000, 141: 2532–2539. 10.1210/en.141.7.2532
Auersperg N, Wong AST, Choi K-C, Kang SK, Leung PCK: Ovarian surface epithelium: biology, endocrinology and pathology. Endocr Rev 2001, 22: 255–288. 10.1210/er.22.2.255
Kossowska-Tomaszczuk K, De Geyter C, De Geyter M, Martin I, Holzgreve W, Scherberich A, Zhang H: The multipotency of leutinizing granulosa cells collected from mature ovarian follicles. Stem Cells 2009, 27: 210–219. 10.1634/stemcells.2008-0233
Motta PM, Heyn R, Makabe S: Three-dimensional microanatomical dynamics of the ovary in postreproductive aged women. Fertil Steril 2002, 78: 360–370. 10.1016/S0015-0282(02)03216-8
Burk K, Dewinko B, Trujillo JM, Ahearn MJ: Establishment of a human plasma cell line in vitro. Cancer Res 1978, 38: 2508–2513.
Hübner K, Fuhrmann G, Christenson LK, Kehler J, Reinbold R, De La Fuente R, Wood J, Strauss JF III, Boiani M, Schöler HR: Derivation of oocytes from mouse embryonic stem cells. Science 2003, 300: 1251–1256.
Boxberger H-J, Meyer T, Grausam M, Reich K, Becker H-D, Sessler MJ: Isolating and maintaining highly polarized epithelial cells from normal human duodenum for growth as spheroid-like vesicles. In Vitro Cell Dev-An 1997, 33: 536–545. 10.1007/s11626-997-0096-0
Song N, Jia X-S, Jia L-L, Ma X-B, Li F, Wang E-H, Li X: Expression and role of Oct3/4, Nanog and Sox2 in regeneration of rat tracheal epithelium. Cell Proliferat 2010, 43: 49–55. 10.1111/j.1365-2184.2009.00653.x
Tai M-H, Chang C-C, Olson LK, Trosko JE: Oct4 expression in adult human stem cells: evidence in support of the stem cell theory of carcinogenesis. Carcinogenesis 2005, 26: 495–502. 10.1093/carcin/bgh321
Zhang S, Balch C, Chan MW, Lai H-C, Matei D, Schilder J, Yan PS, Huang TH-M, Nephew KP: Identification and characterization of ovarian cancerinitiating cells from primary human tumours. Cancer Res 2008, 68: 4311–4320. 10.1158/0008-5472.CAN-08-0364
Bapat S: Human ovarian cancer stem cells. Reproduction 2010, 140: 33–41. 10.1530/REP-09-0389
Bowen NJ, Walker LD, Matyunina LV, Logani S, Totten KA, Benigno BB, McDonald JF: Gene expression profiling supports the hypothesis that human ovarian surface epithelia are multipotent and capable of serving as ovarian cancer initiating cells. BMC Medical Genomics 2009, 2: 71. 10.1186/1755-8794-2-71
Izadyar F, Pau F, Marh J, Slepko N, Wang T, Gonzalez R, Ramos T, Howerton K, Sayre C, Silva F: Generation of multipotent cell lines from a distinct population of male germ line stem cells. Reproduction 2008, 135: 771–784. 10.1530/REP-07-0479
Toyooka Y, Tsunekawa N, Takahashi Y, Matsui Y, Satoh M, Noce T: Expression and intracellular localization of mouse Vasa-homologue protein during germ cell development. Mech Develop 2000, 93: 139–149. 10.1016/S0925-4773(00)00283-5
Durcova-Hills G, Tang F, Doody G, Tooze R, Surani MA: Reprogramming primordial germ cells into pluripotent stem cells. PLoS ONE 2008, 3: e3531. 10.1371/journal.pone.0003531
Qing T, Liu H, Wei W, Ye X, Shen W, Zhang D, Song Z, Yang W, Ding M, Deng H: Mature oocytes derived from purified mouse fetal germ cells. Hum Reprod 2008, 23: 54–61. 10.1093/humrep/dem334
Roby KF, Taylor CC, Sweetwood JP, Cheng Y, Pace JL, Tawfik O, Persons DL, Smith PG, Terranova PF: Development of a syngeneic mouse model for events related to ovarian cancer. Carcinogenesis 2000, 21: 585–591. 10.1093/carcin/21.4.585
Shepherd TG, Thériault BL, Campbell EJ, Nachtigal MW: Primary culture of ovarian surface epithelial cells and ascites-derived ovarian cancer cells from patients. Nature Protocols 2006, 1: 2643–2649. 10.1038/nprot.2006.328
Szotek PP, Chang HL, Brennand K, Fujino A, Pieretti-Vanmarcke R, Lo Celso C, Dombkowsky D, Preffer F, Cohen K, Teixeira J, Donahoe P: Normal ovarian surface epithelial label-retinaing cells exhibit stem/progenitor cell characteristics. P Natl Acad Sci USA 2007, 105: 12469–12473. 10.1073/pnas.0805012105
Dole G, Nilsson EE, Skinner MK: Glial-derived neurotrophic factor promotes ovarian primordial follicle development and cell-cell interactions during folliculogenesis. Reproduction 2008, 135: 671–682. 10.1530/REP-07-0405
Besnard V, Wert S, Hull WM, Whitsett JA: Immunohistochemical localization of Foxa1 and Foxa2 in mouse embryos and adult tissues. Gene Expr Patterns 2004, 5: 193–208. 10.1016/j.modgep.2004.08.006
Su H-Y, Lai H-C, Lin Y-W, Chou Y-C, Liu C-Y, Yu M-H: An epigenetic marker panel for screening and prognostic prediction of ovarian cancer. Int J Cancer 2009, 124: 387–393. 10.1002/ijc.23957
Lawrenson K, Benjamin E, Turmaine M, Jacobs I, Gayther S, Dafou D: In vitro three-dimensional modeling of human ovarian surface epithelial cells. Cell Proliferation 2009, 42: 385–393. 10.1111/j.1365-2184.2009.00604.x
Alton M, Taketo T: Switch from BAX-dependent to BAX-independent germ cell loss during the development of fetal mouse ovaries. J Cell Sci 2007, 120: 417–424. 10.1242/jcs.03332
Hashimoto H, Sudo T, Mikami Y, Otani M, Takano M, Tsuda H, Itamochi H, Katauchi H, Ito M, Nishimura R: Germ cell specific protein VASA is overexpressed in epithelial ovarian cancer and disrupts DNA damage-induced G2 checkpoint. Gynecol Oncol 2008, 111: 312–319. 10.1016/j.ygyno.2008.08.014
Pelloux MC, Picon R, Gangerau MN, Darmoul D: Effects of busulphan on ovarian folliculogenesis, steroidogenesis and anti-Müllerian activity of rat neonates. Acta Endocrinol 1988, 118: 218–226.
Hemsworth BN, Jackson H: Effect of busulphan on the developing ovary in the rat. J Reprod Fert 1963, 6: 229–233. 10.1530/jrf.0.0060229
Hilscher W, Hilscher B: Comparative studies on oogenesis and prespermatogenesis in the Wistar rat under normal and pathological conditions. Ann Biol Anim Biochim Biophys 1973, 13: 127–136. 10.1051/rnd:19730511
Burkl W, Schiechl H: The growth of follicles in the rat ovary under the influence of busulphan and endoxan. Cell Tissue Res 1978, 186: 351–359. 10.1007/BF00225543
Generoso WM, Stout SK, Huff SW: Effects of alkylating chemicals on reproductive capacity of adult female mice. Mutat Res 1971, 13: 171–184.
Choi Y-J, Ok D-W, Kwon D-N, Chung J-I, Kim H-C, Yeo S-M, Kim T, Seo H-G, Kim J-H: Murine male germ cell apoptosis induced by busulfan treatment correlates with loss of c-kit-expression in a Fas/FasL- and p53-independent manner. FEBS Lett 2004, 575: 41–51. 10.1016/j.febslet.2004.08.034
Choi Y-J, Song H, Kwon D-N, Cho S-K, Kang S-J, Yoe S-M, Kim H-C, Lee H-T, Park C, Kim J-H: Significant IgG-immunoreativity of the spermatogonia of the germ cell-depleted testis after busulfan treatment. Anim Reprod Sci 2006, 91: 317–335. 10.1016/j.anireprosci.2005.04.002
Hutt KJ, McLaughlin EA, Holland MK: Kit ligand and c-Kit have diverse roles during mammalian oogenesis and folliculogenesis. Mol Hum Reprod 2006, 12: 61–69. 10.1093/molehr/gal010
Yoshida H, Takakura N, Kataoka H, Kunisada T, Okamura H, Nishikawa S-I: Stepwise requirement of c-kit tyrosine kinase in mouse ovarian follicle development. Dev Biol 1997, 184: 122–137. 10.1006/dbio.1997.8503
Reynaud K, Cortvrindt R, Smitz J, Driancourt M-A: Effects of kit ligand and anti-kit antibody on growth of cultured mouse preantral follicles. Mol Reprod Dev 2000, 56: 483–494. 10.1002/1098-2795(200008)56:4<483::AID-MRD6>3.0.CO;2-O
Kissel H, Timokhina I, Hardy MP, Rothschild G, Angeles G, Whitlow SR, Manova K, Besmer P: Point mutation in Kit receptor tyrosine kinase reveals essential roles for Kit signaling in spermatogenesis and oogenesis without affecting other Kit responses. EMBO J 2000, 19: 1312–1326. 10.1093/emboj/19.6.1312
Hsieh MM, Langemeijer S, Wynter A, Phang OA, Kang EM, Tisdale JF: Lowdose parenteral busulfan provides an extended window for the infusion of hematopoietic stem cells in murine hosts. Exp Hematol 2007, 39: 1414–1420.
Mauch P, Down JD, Warhol M, Hellman S: Recipient preparation for bone marrow transplantation. I. Efficacy of total-body irradiation and busulfan. Transplantation 1988, 46: 205–209. 10.1097/00007890-198808000-00004
Kuramoto K, Follman D, Hematti P, Sellers S, Laukkanen MO, Seggewiss R, Metzger ME, Krouse A, Donahue E, von Kalle C, Dunbar CE: The impact of low-dose busulfan on clonal dynamics in nonhuman primates. Blood 2004, 104: 1273–1280. 10.1182/blood-2003-08-2935
Yoshimizu T, Sugiyama N, De Felice M, Yeom YI, Ohbo K, Masuko M, Scholer HR, Matsui Y: Germline-specific expression of the oct-4/green fluorescent protein (GFP) transgene in mice. Dev Growth Differ 1999, 41: 675–684. 10.1046/j.1440-169x.1999.00474.x
Schöler HR, Hatzopoulos AK, Balling R, Suzuki N, Gruss P: A family of octamer-specific proteins present during mouse embryogenesis: evidence for germline-specific expression of an Oct factor. EMBO J 1989, 8: 2543–2550.
Atlasi Y, Mowla SJ, Ziaee SAM, Gokhale PJ, Andrews PW: Oct4 spliced variants are differentially expressed in human pluripotent and nonpluripotent cells. Stem Cells 2008, 26: 3068–3074. 10.1634/stemcells.2008-0530
Zulli A, Buxton BF, Merrilees M, Hare DL: Human diseased arteries contain cells expressing leukocytic and embryonic stem cell markers. Human Pathol 2008, 39: 657–665. 10.1016/j.humpath.2007.09.022
Zulli A, Rai S, Buxton BF, Burrell LM, Hare DH: Co-localization of angiotensin-converting enzyme 2-, octomer-4- and CD34-positive cells in rabbit atherosclerotic plaques. Exp Physiol 2008, 93: 564–569. 10.1113/expphysiol.2007.040204
Covello KL, Kehler J, Yu H, Gordan JD, Arsham AM, Hu CJ, Labosky PA, Simon MC, Keith B: HIF-2alpha regulates oct-4: effects of hypoxia on stem cell function, embryonic development, and tumor growth. Gene Dev 2006, 1: 557–570. 10.1101/gad.1399906
Koziol M, Garrett N, Gurdon J: Tpt1 activates transcription of oct4 and nanog in transplanted somatic nuclei. Curr Biol 2007, 17: 801–807. 10.1016/j.cub.2007.03.062
Guillaume E, Pineau C, Dupaix A, Moertz E, Sanchez JC, Hochstrasser DF, Jegou B: Cellular distribution of translationally controlled tumor protein in rat and human testis. Proteomics 2001, 1: 880–889. 10.1002/1615-9861(200107)1:7<880::AID-PROT880>3.0.CO;2-2
Wu R, Van der Hoek K, Ryan N, Norman RJ, Robker RL: Macrophage contributions to ovarian function. Hum Reprod Update 2004, 10: 119–133. 10.1093/humupd/dmh011
Gaytán F, Morales C, Bellido C, Aguilar E, Sánchez-Criado JE: Ovarian follicle macrophages: is follicular atresia in the immature rat a macrophage-mediated event? Biology Reprod 1998, 58: 52–59.
Bielanska-Osuchowska Z: Oogonia and oocytes degeneration and the nutritive macrophages in the process of the development of the ovary in embryos of the domestic pig (Sus scrofa dom. L.). Anat Embryol 1973, 142: 37–52. 10.1007/BF00519875
Ni K, O'Neill HC: Improves FACS analysis confirms generation of immature dendritic cells in long-term stromal-dependent spleen cultures. Immunol Cell Biol 2000, 78: 196–204. 10.1046/j.1440-1711.2000.00897.x
Hiyama S-I, Kamiya S, Yamazaki A, Daigo M, Nigi H: Lipofuscin in the corpus luteum of macaque ovaries. Primates 1992, 33: 133–137. 10.1007/BF02382770
Sainte-Marie G: The distribution of the autofluorescent cells and of the yellow autofluorescent granules in the rat tissues. Anat Rec 1965, 153: 71–83. 10.1002/ar.1091530109
Huber TL, Kouskoff V, Fehling HJ, Palis J, Keller G: Haemangioblast commitment is initiated in the primitive streak of the mouse embryo. Nature 2004, 432: 625–630. 10.1038/nature03122
McLaren A: Meiosis and differentiation of mouse germ cells. In Controlling Events in Meiosis, Thirty-eighth Symposium of the Society of Experimental Biology. Edited by: Evans CW, Dickinson HG. The Company of Biologists, Cambridge; 1984:7–23.
Hogan B: Primordial germ cells as stem cells. In Stem Cell Biology. Edited by: Marshak DR, Gardner RL, Gottlieb D. New York: Cold Spring Harbor Laboratory Press; 2001:189–204.
Ohinata Y, Payer B, O'Carroll D, Ancelin K, Ono Y, Sano M, Barton SC, Obukhanych T, Nussenzweig M, Tarakhovsky A, Saitou M, Surani MMA: Blimp1 is a critical determinant of the germ cell lineage in mice. Nature 2005, 436: 207–213. 10.1038/nature03813
Saitou M, Payer B, Lange UC, Erhardt S, Barton SC, Surani AM: Specification of germ cell fate in mice. Philos T Roy Soc B 2003, 358: 1363–1370. 10.1098/rstb.2003.1324
Greenbaum MP, Iwamori N, Agno J, Matzuk MM: Mouse TEX14 is required for embryonic germ cell intercellular bridges but not female fertility. Biol Reprod 2009, 80: 449–457. 10.1095/biolreprod.108.070649
Bronson RA, Fusi FM, Fleit HB: Identification of an oolemmal IgG Fc receptor: its role in promoting binding of antibody-labeled human sperm to zona-free hamster eggs. Am J Reprod Immunol 1990, 23: 876–892.
Bronson RA, Fusi FM, Fleit HB: Monoclonal antibodies identify Fc gamma receptors on unfertilized human oocytes but not spermatozoa. J Reprod Immunol 1992, 21: 293–307. 10.1016/0165-0378(92)90032-Y
Ravetch JV: Fc receptors: rubor redux. Cell 1994, 78: 553–560. 10.1016/0092-8674(94)90521-5
Daëron M: Fc receptor biology. Annu Rev Immunol 1997, 15: 203–234.
Kanatsu-Shinohara M, Ogonuki N, Inoue K, Miki H, Ogura A, Toyokuni S, Shinohara T: Long-term proliferation in culture and germline transmission of mouse male germline stem cells. Biol Reprod 2003, 69: 612–616. 10.1095/biolreprod.103.017012
Hashimoto K, Noguchi M, Nakatsuji N: Mouse offspring derived from fetal ovaries or reaggregates which were cultured and transplanted into adult females. Dev Growth Differ 1992, 43: 233–238. 10.1111/j.1440-169X.1992.tb00012.x
Kawase E, Shirayoshi Y, Hashimoto K, Nakatsuji N: A combination of Buffalo rat liver cell-conditioned medium, forskolin and membrane-bound stem cell factor stimulates rapid proliferation of mouse primordial germ cells in vitro similar to that in vivo. Dev Growth Differ 1996, 38: 315–322. 10.1046/j.1440-169X.1996.t01-2-00011.x
Ohkubo Y, Shirayoshi Y, Nakatsuji N: Autonomous regulation of proliferation and growth arrest in mouse primordial germ cells studies by mixed and clonal cultures. Exp Cell Res 1996, 222: 291–297. 10.1006/excr.1996.0037
Nakatsuji N, Chuma S: Differentiation of mouse primordial germ cells into female or male germ cells. Int J Dev Biol 2001, 45: 541–548.
Wang H, Xia G, Wang Q, Li M, Lu Z: Follicles were reconstituted from dissociated mouse fetal ovarian cells in vitro. Chinese Sci Bull 2001, 46: 672–674. 10.1007/BF03182833
Haston KM, Tung JY, Reijo Pera RA: Dazl functions in maintenance of pluripotency and genetic and epigenetic programs of differentiation in mouse primordial germ cells in vivo and in vitro. PLoS ONE 2009, 4: e5654. 10.1371/journal.pone.0005654
Manova K, Bacharova RF: Expression of c-kit encoded at the W locus of mice in developing embryonic germ cells and presumptive melanoblasts. Dev Biol 1991, 146: 312–324. 10.1016/0012-1606(91)90233-S
Resnick JL, Ortiz M, Keller JR, Donovan P: Role of fibroblast growth factors and their receptors in mouse primordial germ cell growth. Biol Reprod 1998, 59: 1224–1229. 10.1095/biolreprod59.5.1224
Driancourt M-A, Reynaud K, Cortvrindt R, Smitz J: Roles of KIT and KIT LIGAND in ovarian function. Rev Reprod 2000, 5: 143–152. 10.1530/ror.0.0050143
Baltus AE, Menke DB, Hu Y-C, Goodheart ML, Carpenter AE, de Rooij DG, Page DC: In germ cells of mouse embryonic ovaries, the decision to enter meiosis precedes premeiotic DNA replication. Nat Genet 2006, 38: 1430–1434. 10.1038/ng1919
Hoyer PE, Byskov AG, Mollgard K: Stem cell factor and c-kit in human primordial germ cells and fetal ovaries. Mol Cell Endocrinol 2005, 234: 1–10. 10.1016/j.mce.2004.09.012
Lou Y-H, Park K-K, Agersborg S, Alard P, Tung KSK: Retargeting T cellmediated inflammation: a new perspective on autoantibody action. J Immunol 2000, 164: 5252–5257.
Samy E, Parker LA, Sharp CP, Tung KSK: Continuous control of autoimmune disease by antigen-dependent polyclonal CD4+ CD25+ regulatory T cells in the regional lymph node. J Exp Med 2005, 202: 771–781. 10.1084/jem.20041033
Wheeler KM, Samy ET, Tung KSK: Normal regional lymph node enrichment of antigen-specific regulatory cells with autoimmune disease suppressive capacity. J Immunol 2009, 183: 7635–7638. 10.4049/jimmunol.0804251
Tung KSK, Lou YH, Farza KM, Teuscher C: Autoimmune ovarian disease: mechanism of disease induction and prevention. Curr Opin Immunol 1997, 9: 839–845. 10.1016/S0952-7915(97)80187-2
Masteller EL, Tang Q, Bluestone JA: Antigen-specific regulatory T cells - ex vivo expansion and therapeutic potential. Semin Immunol 2006, 18: 103–110. 10.1016/j.smim.2006.01.004
MacKay IR, Leskovsek NV, Rose NR: Cell damage and autoimmunity: a critical appraisal. J Autoimmun 2008, 30: 5–11. 10.1016/j.jaut.2007.11.009
Brode S, Raine T, Zaccone P, Cooke A: Cyclophosphamide-induced type-1 diabetes in the NOD mouse is associated with a reduction of CD4+ CD25+ Foxp3+ regulatory T cells. J Immunol 2006, 177: 6603–6612.
Nakahara T, Uchi H, Lesokhin AM, Avogadri F, Rizzuto GA, Hirschhorn-Cymerman D, Panageas KS, Merghoub T, Wolchok JD, Houghton AN: Cyclophosphamide enhances immunity by modulating the balance of dendritic cell subsets in lymphoid organs. Blood 2010, 115: 4384–4392. 10.1182/blood-2009-11-251231
Sedmak DD, Hart WR, Tubbs RR: Autoimmune oophoritis: a histopathologic study of involved ovaries with immunologic characterization of the mononuclear cell infiltrate. Int J Gynecol Pathol 1987, 6: 73–83. 10.1097/00004347-198703000-00009
Melner MH, Feltus FA: Autoimmune premature ovarian failure- endocrine aspects of T cell disease. Endocrinology 1999, 140: 3401–3403. 10.1210/en.140.8.3401
Lebovic DI: Premature ovarian failure: think "autoimmune disorder". Sex Reprod Menopause 2004, 2: 230–233. 10.1016/j.sram.2004.11.010
Kaminitz A, Mizrahi K, Yaniv I, Farkas DL, Stein J, Askenasy N: Low levels of allogeneic but not syngeneic hematopoietic chimerism reverse autoimmune insulitis in prediabetic NOD mice. J Autoimmun 2009, 33: 83–91. 10.1016/j.jaut.2009.07.001
Chan J, Ban EJ, Chun KH, Wang S, Bäckström BT, Bernard CCA, Toh BH, Alderuccio F: Transplantation of bone marrow transduced to express self antigen establishes deletional tolerance and permanently remits autoimmune disease. J Immunol 2008, 181: 7571–7580.
Alderuccio F, Chan J, Scott DW, Toh B-H: Gene therapy and bone marrow stem-cell transfer to treat autoimmune disease. Trends Mol Med 2009, 15: 344–351. 10.1016/j.molmed.2009.06.002
Yaniv I, Ash S, Farkas DL, Askenasy N, Stein J: Consideration of strategies for hematopoietic cell transplantation. J Autoimmun 2009,33(3–4):255–259.
Beilhack GF, Scheffold YC, Weissman IL, Taylor C, Jerabek L, Burge MJ, Masek MA, Shizuru JA: Purified allogeneic hematopoietic stem cell transplantation blocks diabetes pathogenesis in NOD mice. Diabetes 2003, 52: 59–68. 10.2337/diabetes.52.1.59
Zou L, Barnett B, Safah H, LaRussa VF, Evdemon-Hogan M, Mottram P, Wei S, David O, Curiel TJ, Zou W: Bone marrow is a reservoir for CD4+CD25+ regulatory T cells that traffic through CXCL12/CXCR4 signals. Cancer Res 2004, 64: 8451–8455. 10.1158/0008-5472.CAN-04-1987
Salem ML, AL-Khami AA, EL-Naggar SA, Chen Y, Cole DJ: Cyclophosphamide induces dynamic alteration in the host microenvironments resulting in a Flt3 ligand-dependent expansion of dendritic cells. J Immunol 2010, 184: 1737–1747. 10.4049/jimmunol.0902309
Di Giacomo M, Barchi M, Baudat F, Edelmann W, Keeney S, Jasin M: Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants. P Natl Acad Sci USA 2005, 102: 737–742. 10.1073/pnas.0406212102
Barchi M, Roig I, Di Giacomo M, de Rooij DG, Keeney S, Jasin M: ATM promotes the obligate XY crossover and both crossover control and chromosome axis integrity on autosomes. PLoS Genetics 2008, 4: e1000076. 10.1371/journal.pgen.1000076
Oktay K, Oktem O: Regeneration of oocytes after chemotherapy: connecting the evidence from mouse to human. J Clin Oncol 2007, 25: 3185–3187. 10.1200/JCO.2007.11.5097
McLaren A, Southee D: Entry of mouse embryonic germ cells into meiosis. Dev Biol 1997, 187: 107–113. 10.1006/dbio.1997.8584
Wu J, Zhang Y, Tian GG, Zou K, Lee CM, Yu Q, Yuan Z: Short-type PBcadherin promotes self-renewal of spermatogonial stem cells via multiple signaling pathways. Cell Signal 2008, 20: 1052–1060. 10.1016/j.cellsig.2008.01.011
Luciani JM, Devictor M, Stahl A: Preleptotene chromosome condensation in human foetal and neonatal testes. J Embryol Exp Morph 1977, 38: 175–186.
Wartenberg H, Hilscher B, Hilscher W: Germ cell kinetics during early ovarian differentiation: an analysis of the oogonial cell cycle and the subsequent changes in oocyte development during the onset of meiosis in the rat. Microsc Res Techniq 1998, 40: 377–397. 10.1002/(SICI)1097-0029(19980301)40:5<377::AID-JEMT5>3.0.CO;2-O
Yamada K: Conversion of mitotic to meiotic cells in Saccharomyces cerevisiae. II. Relation between premeiotic DNA replication and revertibility to mitosis. Plant Cell Physiol 1983, 24: 1017–1026.
The author is much indebted to Robert M. Moor for inspiring this article, and for his unstinting support and expert advice; and to Roger G. Gosden and Rus Hoelzel for their critical appraisal of the manuscript and most helpful suggestions. This article is dedicated to the memory of H. B. F. Dixon.
The author declares that she has no competing interests.