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Whether the adult mammalian ovary contains oogonial stem cells (OSCs) is controversial. They have been isolated by a live-cell sorting method using the germ cell marker DDX4, which has previously been assumed to be cytoplasmic, not surface-bound. Furthermore their stem cell and germ cell characteristics remain disputed. Here we show that although OSC-like cells can be isolated from the ovary using an antibody to DDX4, there is no good in silico modelling to support the existence of a surface-bound DDX4. Furthermore these cells when isolated were not expressing DDX4, and did not initially possess germline identity. Despite these unremarkable beginnings, they acquired some pre-meiotic markers in culture, including DDX4, but critically never expressed oocyte-specific markers, and furthermore were not immortal but died after a few months. Our results suggest that freshly isolated OSCs are not germ stem cells, and are not being isolated by their DDX4 expression. However it may be that culture induces some pre-meiotic markers. In summary the present study offers weight to the dogma that the adult ovary is populated by a fixed number of oocytes and that adult de novo production is a rare or insignificant event.
The prevailing dogma in the field of reproductive biology for over 60 years has been that the adult mammalian ovary lacks germ stem cells1. This has been used to explain why women undergo the menopause, and suffer from premature ovarian failure if the primordial follicle pool is depleted by chemotherapy2,3. However, such dogma was challenged by Tilly and coworkers, who following genotoxic drug treatment observed a re-establishment of the primordial follicle pool in mice4. Controversy over such a fundamental paradigm shift followed5,6, and included contrary observations as to whether germ cells were resident in the ovary or migrated from other tissues7,8, with some groups reporting no re-establishment of the follicle pool by adult germ cells in physiological and pathological conditions9,10.
Support for the existence of ovarian cells with germ stem cell identity, which have been named Oogonial Stem Cells (OSCs), came with their isolation from the ovary11,12. OSCs developed meiotic markers in culture and formed oocyte-like cells11,12,13; they could be transplanted into mouse ovaries where they assembled into follicles12, and they could go on to form live pups when fertilized11. However controversy continues as other studies using similar methods of isolation have failed to replicate any of these findings, and instead they culture cells that senesce and are non-germline in origin14,15,16.
OSCs have been sorted (FACS or MACS) from ovarian tissue in most studies with an antibody to DDX4 (DEAD (Asp-Glu-Ala-Asp) box polypeptide 4)11,12,13,14,17,18,19,20. DDX4 is a germline-specific RNA helicase, containing a DEADc ATP hydrolysis domain and a HELICc RNA-binding domain that are common to all members of the DEAD box protein family21,22. Adding to the continuing controvery over the existence of OSCs is that DDX4 as an RNA binding protein was hitherto believed to be cytoplasmic23,24, rather than membrane-bound, and as such it has been unclear how it can be effective in sorting live cells.
In this study we examine the specificity of the DDX4 antibody used to isolate OSCs. We find that it can be used to sort a small population of ovarian cells which appear to take on some characteristics of OSCs following culture. However these characteristics are found either not to be germ-cell-specific or are initially absent from freshly sorted cells. Importantly cultured cells senesce and fail to develop any characteristics of oocytes or possess oocyte-specific markers. Furthermore we demonstrate that their initial isolation is not due to any cell surface expression of DDX4.
An anti-DDX4 antibody raised against the C-terminal 25 residues of human DDX4 (here onwards defined as DDX4C25 antibody) has been used to isolate by MACS or FACS a small population of OSCs from adult ovary in mouse11,12,13,14,17,18,19,20,25. The C-terminus shares high sequence homology between human and mouse, making this possible (Fig. 1A).
As expected based on its known function as an RNA-binding protein22, immunohistochemical staining with the DDX4C25 antibody in permeabilized fully-grown oocytes from antral follicles, revealed a cytoplasmic distribution (Fig. 1B). This was absent in non-permeabilized oocytes, with no evidence of any surface staining (Fig. 1C). Similarly as expected of a germline-specific protein, DDX4 appeared absent from ovarian granulosa cells, independent of their permeabilization status (Fig. 1B,C).
The DDX4C25 antibody has been used by others11,12,13,14,17,18,19,20 to isolate OSCs by FACS. This assumes a membrane-bound form of DDX4 is being expressed in the female germ stem cells, and the C-terminal epitope is exposed to the extracellular milieu to allow affinity-antibody binding. This idea, although never reported in any detail, has often been quoted as being supported by transmembrane modelling11,26. While this membrane-bound form of DDX4 appears absent from fully-grown oocytes (Fig. 1B), this has been suggested to be due to a differentiation-dependent internalization of the protein12.
Here we report for the first time on a comprehensive in silico examination of the evidence for a transmembrane DDX4 protein. We ran a number of online transmembrane domain predictors on both the human and mouse DDX4 to determine how robust the existence of a C-terminal extracellular domain was. Eleven methods that combined different statistical models and discriminative analysis of protein topology were used (Supplementary Table S1). In human, three methods predicted a transmembrane domain, but all three placed the C-terminus in the cytoplasm, not on the cell surface (Supplementary Fig. S1, Supplementary Table S2). In mouse (Supplementary Table S3), four methods predicted a transmembrane domain, with three of these placing the C-terminus in the cytoplasm (Supplementary Fig. S1). TMpred was the method used previously to justify the cell surface location of the OSCs11,26, and is the sole model to predict an extracellular C-terminal domain but only in mouse, not human (Supplementary Table S3, Supplementary Fig. S1). We conclude therefore that the evidence of a transmembrane DDX4 that could be isolated by the DDX4C25 antibody is non-existent in humans, and weak in mouse.
The above modelling shows that the majority of programs predict no membrane-bound DDX4 with an extracellular C-terminus. However, given one model that does, albeit in mouse not human, we attempted to FACS-sort cell surface DDX4C25-positive cells from a total mouse ovarian cell suspension. To our surprise we were able to isolate a small population of DDX4C25-positive cells that were 2.5±0.6% (mean±s.e.m.) (range 0.1% to 6.6%) of the total number of viable cells sorted (n=10 independent FACS; Fig. 2A, Supplementary Fig. S2). These sorted cells, which ranged from 23 to 8,281 cells per experiment, were seeded for further analysis.
To characterise the DDX4C25-positive cells they were immunostained using a number of germline markers: DDX4 (using DDX4C25 antibody), PRDM1 (also known as BLIMP1; PR domain containing 1, with ZNF domain), DPPA3 (also known as STELLA; developmental pluripotency-associated 3), IFITM3 (also known as FRAGILIS; interferon induced transmembrane protein 3) and DAZL (deleted in azoospermia-like). These antibodies were all positive when tested on fixed and permeabilized fully grown oocytes (Fig. 1, Supplementary Fig. S2).
We analysed the primary cultures of DDX4C25-positive cells, which some groups are describing as OSCs11,12,14,17. In non-permeabilized putative OSCs there was cell surface immunostaining using the DDX4C25 antibody (n=3, Fig. 2B), a finding which confirms that the ovary does indeed contain cells with a DDX4C25 cell surface epitope. In the DDX4C25-positive cells we could not detect DPPA3 or DAZL (Fig. 2B). However, these cells did have immunostaining for PRDM1 and IFITM3, a finding which has been reported on previously11,12. Importantly, ovarian somatic cells that had been separated as DDX4C25-negative cells during FACS, also stained positively for PRDM1 and IFITM3 (Supplementary Fig. S2). As such we conclude that both PRDM1 and IFITM3 are not exclusive markers of the germline, as they appear to be present in many ovarian cells.
Although the primary cultures of putative OSCs had a cell surface DDX4C25 epitope, and were also immunopositive for PRDM1 and IFITM3 in their cytoplasm, they appeared to lack detectable levels of other germ cell markers such as DPPA3 and DAZL. Previous studies have not reached a consensus over whether freshly sorted putative OSCs already express these germline markers, with some studies demonstrating expression11,12,14,17,19,25 and others not15,16.
To determine if ex-vivo culture was important for the generation of germline markers, gene expression analysis was performed on freshly sorted and 2-month-old putative OSCs. Specifically we examined for germline markers (Prdm1, Dppa3, Ifitm3, Ddx4, Dazl), pluripotency markers (Pou5f1/Oct4; POU domain, class 5, transcription factor 1), meiosis markers (Stra8; stimulated by retinoic acid gene 8) and oocyte markers (Nobox, NOBOX oogenesis homeobox; Zp3, zona pellucida glycoprotein 3). To calibrate the sensitivity of our detection, RNA from total ovarian cell extracts was used at various concentrations (0.1–30ng). Testis was used as a positive control for all of the germline, pluripotency, and meiosis markers, and the ribosomal gene Rps29 (ribosomal protein S29) was used as a positive control for each cDNA preparation27.
The gene expression profile of germline, pluripotency and oocyte-specific markers in the ovary and testis were all as expected. Of all these markers only Stra8 was absent from the ovary. Stra8 is associated with entry into meiosis but not oocyte maturation, and as such would be predicted to be absent from the adult ovary, which already contains meiosis-committed immature oocytes28,29. The testis expressed all markers except the oocyte-specific Zp3 and Nobox (Fig. 2C)12,17. Zp3 is an oocyte-specific extracellular protein that forms part of the zona pellucida30, and as such would be absent from the testis, as would Nobox which is an oocyte-specific homeobox protein31.
Freshly sorted putative OSCs only expressed Ifitm3 (Fig. 2C), which confirms the immunostaining. However, although often used as a germline marker, is not exclusive to the germline32,33, and can be observed in explants of dermal mouse fibroblasts. Even though OSCs were isolated on the basis of their cell surface DDX4C25-positive antigen, they were negative for Ddx4. Furthermore these cells were negative for all the other germline, pluripotency and oocyte-specific markers. We conclude that freshly isolated putative OSCs that are categorised as DDX4-positive cells by possessing an externalised DDX4C25 epitope, do not express Ddx4 and furthermore show no characteristics that would appear to give them a hallmark of being germ stem cells.
Interestingly, after 2 months in culture the putative OSCs also started to express Prdm1, Ddx4 and Pou5f1 (Fig. 2C). It is difficult to conclude only on this expression profile that such cells are stem cells, given dermal fibroblasts were also positive for Prdm1. It may be what we take as markers of germline are more ubiquitous than previously thought. Furthermore there was no commitment to meiosis or oogenesis, judged by the lack of Stra8, Nobox, and Zp3 (n=7). We observed that approximately 2–3 months after isolation, all the OSCs cultures decreased their growth rate and died. Therefore, the sorted cells were not immortalised.
One study, using the DDX4C25 antibody, has reported on the existence of DDX4-positive cells in the oviductal epithelium34. We could also observe staining in the cytoplasm of permeabilized epithelial cells from oviductal sections (Fig. 3A and insert), but not in non-permeabilized, individual cells (Supplementary Fig. S3). Immunohistological staining of ovarian sections also revealed specific DDX4C25 immunoreactivity in oocytes from various stages of growth (Supplementary Fig. S3 and insert). Therefore the antibody used seems specific on sections, and indeed does detect DDX4C25-positive oviductal epithelium cells.
PRDM1 and IFITM3 staining were also observed in the oviductal epithelium (Fig. 3A). Whereas PRDM1 showed a homogeneous presence, IFITM3 was only in those cell surfaces in contact with the lumen (Fig. 3A and insert). PRDM1 staining was ubiquitously seen in oocytes, stromal and granulosa cells of the ovary, and in the tubules of the embryonic kidney (Supplementary Fig. S3 and inserts). IFITM3 staining was also observed in oocytes, stromal cells of the ovary, and in the cells next to the tubules in the embryonic kidney (Supplementary Fig. S3 and inserts). This localization in somatic tissues shows that IFITM3 and PRDM1 do not confer a germline identity. DPPA3 and DAZL were also present in oocytes (Supplementary Fig. S3), but were absent from the oviduct and the kidney (Fig. 3A; Supplementary Fig. S3).
The absence of DPPA3 and DAZL from oviductal epithelia suggested that this tissue was devoid of germ stem cells. However, DDX4 staining led us to think that either there were non-germline DDX4-expressing cells in the reproductive tract, or that the DDX4C25 antibody was not specific to DDX4 protein. The latter was our preferred hypothesis, given that the putative OSCs, isolated by FACS using DDX4C25 did not express DDX4 (Fig. 2C). To discriminate between these two possibilities, we performed gene expression analysis on oviduct, flushed extensively to remove any ovulated oocytes that may lead to misinterpretation of results. This was compared with ovary, testis, and cultured fibroblasts. Confirming the immunofluorescence, Prdm1 and Ifitm3 were present in the oviduct, resembling the profile from primary fibroblasts (Fig. 3B), and confirming that these often used germline markers are not germline-specific. The lack of Zp3 and Nobox in oviductal epithelium assured us that oocytes were indeed absent from this tissue preparation (Fig. 3B).
Importantly the absence of Ddx4 in oviductal tissue (Fig. 3B), where the DDX4C25 antibody had abundantly cross-reacted on tissue sections suggested that this antibody hitherto used for DDX4 may readily cross-react with other proteins.
In both the putative OSCs isolated by FACS of whole ovary, and in oviductal epithelial cells DDX4 immunostaining was achieved using a DDX4C25 antibody raised against its C-terminus. However, by PCR neither cell types expressed Ddx4. We speculated that the antibody may be cross-reacting against an unrelated protein epitope. To examine this possibility further we employed a second DDX4 antibody, which is raised against a much larger C-terminal peptide (defined as DDX4351; Supplementary Fig. S4).
DDX4351 antibody was used on both permeabilized oviduct sections and on permeabilized putative OSCs isolated by FACS using DDX4C25 antibody (Fig. 4A). Oocytes at all stages of growth showed high levels of cytoplasmic DDX4351 staining, however neither oviduct nor isolated OSCs were ever observed to be DDX4-positive (Fig. 4B).
This study has shown that the primary technique for isolating adult germline stem cells from the ovary is based on a false assumption: the existence of cell surface DDX4 allowing isolation by FACS. Here we demonstrate that although the antibody can be used to isolate a small population of ovarian cells, these cells are not expressing DDX4.
Given their functions in RNA metabolism, the DEAD-box RNA helicase family including DDX4, is generally cytoplasmic21,22 except for Lactobacillus aggH, which contains a cell surface domain for bacterial aggregation35, and for HEL-T in immature thymocytes, the only known example of development-dependent cell surface expression of a T cell-specific RNA/DNA helicase36. Our computational analysis of transmembrane domains of DDX4 supports such a cytoplasmic localization, and lends little evidence for a C-terminal domain that can be used for the FACS-sorting of OSCs. The TMpred model that has previously justified the OSC FACS technique11,26, reports the externalization of the C-terminus only in mouse, not human, DDX4, and brings into question its ability to sort human OSCs12,37. The mouse double-transmembrane conformation, which allows an external C-terminus should also be regarded as doubtful, because this also necessitates an external N-terminal domain that was previously thought to not exist12, leaving an alternative, weaker conformation to explain the mouse OSC sorting.
Only Prdm1 and Iftm3, often regarded as germline markers38, were present in freshly isolated ovarian cells following FACS with DDX4C25 antibody. Prdm1 is the key regulator of primordial germ cells (PGCs) in the embryo39 but it is also linked to stem cell pluripotency and maturation in non-germline cells40,41,42,43,44,45,46,47,48. Here it was not a specific marker of the germline as it could be detected in dermal fibroblasts. Although PRDM1 has previously often been described as nuclear, it can associate with Prmt5 and together translocate to the cytoplasm for epigenetic reprogramming of PGCs49. It may be that this mechanism, or an equivalent, is leading to the perinuclear distribution observed here. Ifitm3 is also involved in the differentiation of the first PGCs in the embryo50 but has been reported in somatic tissues also to mediate immune responses to viruses, either preventing the cytosolic entry33 or restricting the early replication of influenza A and flaviviruses32. On the contrary, Dppa3, Ddx4 and Dazl have no somatic expression, and they appear to refine the functionality of PGCs to produce oocytes: Dppa3 helps to maintain pluripotency51, whereas Ddx4 and Dazl maintain the proliferation of germ stem cells52,53 and cause entry into meiosis54,55,56. Therefore, expression of Prdm1 and Ifitm3 should not be correlated with an adult germ stem cell identity in the absence of corroborative markers such as Dppa3, Ddx4 and Dazl.
Interestingly, some groups have used IFITM3 to MACS-sort OSCs instead of DDX457,58,59,60. The ubiquitous expression that we have observed here in the ovary, oviduct and kidney suggests that this is not an ideal method, and may additionally isolate somatic cells.
Since some pre-meiotic markers, including Ddx4, were activated in cultured OSCs, but not in DDX4C25-negative cells cultured for the same period of time (data not shown), we speculate that culture may have some effect on the ability of the OSCs to self-reprogram, also proposed by Hernandez et al14.We conclude that OSCs isolated using DDX4C25 antibody are a subpopulation of somatic ovarian cells, containing a reactive uncharacterised epitope – this may be a member of the DDX family but is not DDX4. These cells can establish DDX4 expression in culture, but die without developing germline markers. It is possible that such expression is a product of continued culture, rather than an inherent property of the cells themselves, which turns on DDX4 expression. It is highly unlikely that these putative OSCs play any physiological role in maintaining any adult oocyte pool as first reported 4, and when isolated show no redeeming features to suggest they have stem cell capacity.
C57BL/6 three-to-four-weeks-old female mice, 12-to-20-weeks-old male mice and time-mated E16.5 embryos (Charles Rivers, UK) were used. All experimental protocols were approved by the University of Southampton Animal Ethics Committee and carried out in accordance with UK Home Office regulations and the UK Animals (Scientific Procedures) Act of 1986 (ASPA) under UK Home Office licences.
For each FACS, 12 ovaries were digested, blocked and incubated with 1:10 rabbit DDX4C25 antibody (ab13840; Abcam) adjusted to a concentration of 1mgmL−1, then washed and incubated with 1:250 Alexa Fluor 633 goat anti-rabbit IgG (A21070; Invitrogen, UK). Putative OSCs were sorted using a BD Biosciences FACSAria I (Beckton Dickinson, UK) cytometer, after gating the negative controls (Supplementary Fig. S2)58. Data were analysed using the FLOWJO software (FLOWJO LLC, USA).
FACS-sorted DDX4C25-positive cells were seeded onto MEF-free 24-well plates (Corning, UK) and cultured in OSC culture medium as described previously58.
Formaldehyde-fixed tissue sections, DDX4C25-positive cells and oocytes were incubated with antibodies for the detection of DAZL (ab34139; Abcam), DDX4 (DDX4C25 antibody, ab13840; Abcam and DDX4351 antibody, 17545-1-AP; ProteinTech, UK), DPPA3 (ab19878; Abcam), IFITM3 (ab15592; Abcam) and PRDM1 (PA5-20310; ThermoFisher, UK). All images were acquired using a Leica SP8 microscope with hybrid detectors and x63 oil immersion lens. Fluorochromes were imaged sequentially. Images were then analysed on ImageJ (NIH, USA).
Total RNA was isolated with TRIzol reagent (Life Technologies, UK) and reverse-transcribed with M-MLV Reverse Transcriptase (Promega, UK). Assessment of gene expression was performed by conventional polymerase chain reaction (PCR) using GoTaq DNA Polymerase (Promega, UK). Primer sequences and PCR conditions can be found in the SI Materials and Methods.
All experiments were independently replicated at least three times. Data from the FACS sorting replicates were expressed as the mean±s.e.m. and calculated on GraphPad Prism (GraphPad Software, Inc., USA).
How to cite this article: Zarate-Garcia, L. et al. FACS-sorted putative oogonial stem cells from the ovary are neither DDX4-positive nor germ cells. Sci. Rep. 6, 27991; doi: 10.1038/srep27991 (2016).
This study was supported by a grant to K.T.J. from the University of Southampton.
Author Contributions K.T.J., S.I.R.L., J.A.M. and L.Z.-G. designed research; L.Z.-G. performed research; J.A.M. and L.Z.G. contributed new reagents/analytic tools; K.T.J., S.I.R.L. and L.Z.-G. analysed data; K.T.J., S.I.R.L., J.A.M. and L.Z.-G. wrote the paper.