The role of stem cells in tissue maintenance is appreciated and hierarchical models of stem cell self-renewal and differentiation often proposed. Stem cell activity in the male germline is restricted to undifferentiated A-type spermatogonia (Aundiff); however, only a fraction of this population act as stem cells in undisturbed testis and Aundiff hierarchy remains contentious. Through newly developed compound reporter mice, here we define molecular signatures of self-renewing and differentiation-primed adult Aundiff fractions and dissect Aundiff heterogeneity by single-cell analysis. We uncover an unappreciated population within the self-renewing Aundiff fraction marked by expression of embryonic patterning genes and homeodomain transcription factor PDX1. Importantly, we find that PDX1 marks a population with potent stem cell capacity unique to mature, homeostatic testis and demonstrate dynamic interconversion between PDX1+ and PDX1− Aundiff states upon transplant and culture. We conclude that Aundiff exist in a series of dynamic cell states with distinct function and provide evidence that stability of such states is dictated by niche-derived cues.
Limited lifespan of differentiated cells in many tissues necessitates replacement to ensure tissue maintenance. Within such high turnover tissues, resident stem cells generate fresh cohorts of differentiating cells. Stem cell populations can be heterogeneous and composed of multiple pools with distinct functional characteristics and involvement in tissue maintenance and repair1. Stem cell activity can also be context dependent1. The ability to define different stem cell subsets within a tissue is dependent on availability of molecular markers that delineate populations.
Sustained spermatogenesis and recovery of fertility following germ cell depletion are dependent on stem cells within the testis seminiferous epithelium2. In adult mice, germline stem cell activity is contained within a population of undifferentiated Type A spermatogonia (Aundiff), which develop postnatally from foetal germ cells (gonocytes). Gonocytes migrate from the lumen of developing seminiferous tubules to the basement membrane and generate undifferentiated and differentiating spermatogonia. The adult Aundiff pool contains isolated single cells (A-single or As) plus chains of cells remaining interconnected by cytoplasmic bridges after cell division; 2-cell chains are A-paired (Apr) while chains of 4 or more A-aligned (Aal). Aundiff differentiation is marked by induction of c-KIT plus DNA methyltransferases 3A and 3B (DNMT3A/3B) and formation of A1 spermatogonia3. A1 cells undergo a series of mitotic divisions and via A2, A3, A4, Intermediate (In) and B spermatogonia generate meiotic spermatocytes. It is generally accepted that germline stem cell activity is contained within the Aundiff pool. However, Aundiff cells are heterogeneous and contrasting models of Aundiff hierarchy and stem cell identity are proposed4,5.
A founding model of spermatogonial hierarchy proposed that As act as stem cells while Apr and Aal, the bulk of Aundiff, are differentiation-committed progenitors2. Upon division, As generate two As for self-renewal or Apr that generate Aal and differentiate. This model has been challenged through transplantation and lineage tracing. Germline stem cells form long-lived spermatogenic colonies when injected into seminiferous tubules of germ cell-depleted recipients6. As each colony is normally derived from a single cell, stem cell numbers in the donor population can be estimated. While there are ~35,000 As in an adult testis, only ~3000 cells have transplant capability7, suggesting that not all As are stem cells. Recent studies concluded that transplant activity is almost exclusively contained within a fraction of As marked by Id4 expression, supporting a revised As model in which stem cell activity is limited to a subset of As while remaining As plus Apr and Aal are differentiation-committed or transiting into a committed state5,8. Given that dynamics of Id4 expression are poorly understood and relationship between transplantation capacity and in situ stem cell activity is contentious8,9, it remains to be determined whether ID4+ As solely possess stem cell potential. Studies on ID4+ spermatogonia have often focused on neonates rather than adults5,8.
An alternative stem cell model is proposed based on in situ lineage tracing and live-cell imaging4. Namely, that stem cell potential is a dynamic property shared by most Aundiff irrespective of morphology but that gene expression dictates fate propensity. Aundiff expressing Gfra1 (a co-receptor for glial cell line derived neurotrophic factor or GDNF) that are mostly As, Apr and some short Aal, form an equipotent stem cell pool and transition between single cells and syncytial states10. Aundiff expressing Neurogenin3 (Ngn3), primarily Aal plus few As and Apr, are differentiation-destined due to expression of RARγ and sensitivity to the differentiation stimulus retinoic acid (RA)4,11. GFRα1− progenitors are also marked by transcription factor SOX312. However, during testis regeneration or upon transplantation, NGN3+ cells contribute significantly to the stem cell pool9. NGN3+ Aal can fragment to shorter chains or As and revert to a GFRα1+ state, indicating that NGN3+ cells possess latent stem cell activity4. Further, subsets of NGN3+ cells marked by MIWI2 exhibit regenerative capacity but are dispensable for tissue homeostasis13. Whether stem cell potential is an inherent property of all Aundiff or restricted to a subset of cells remains to be confirmed. Regardless, stem cell activity in undisturbed tissue is primarily associated with the GFRα1+ pool while remaining Aundiff are differentiation-primed.
Niche-derived stimuli and intrinsically expressed factors regulate Aundiff self-renewal and differentiation. Supporting Sertoli cells produce GDNF, which is required for stem cell self-renewal14. Basic fibroblast growth factor (bFGF) is derived from a variety of cells and maintains Aundiff function in concert with GDNF6. Importantly, GDNF and bFGF support long-term culture of Aundiff6. These factors promote Aundiff self-renewal via induction of cell cycle genes plus transcription factors BCL6B, ETV5 and LHX115,16,17,18. Promyelocytic leukaemia zinc finger (PLZF or ZBTB16) promotes Aundiff self-renewal and is an Aundiff marker19,20,21. The transcription factor SALL4, a component of the pluripotency network of embryonic stem cells (ESCs) is expressed throughout the spermatogonial pool and essential for Aundiff differentiation and self-renewal22,23. Other pluripotency-associated factors such as Oct4 (Pou5f1) are expressed in Aundiff and have functional roles24. While multiple genes are involved in Aundiff self-renewal and differentiation, our understanding of mechanisms underlying functional heterogeneity of Aundiff is limited.
Germline stem cell identity remains contentious largely due to our inadequate understanding of Aundiff heterogeneity and limited markers to discriminate functionally distinct Aundiff fractions. To address this heterogeneity at the molecular and functional level and shed light on spermatogonial hierarchy, we generated compound reporter mice based on Plzf and Oct4 promoters that have distinct expression patterns within adult Aundiff. These allowed us to isolate and define gene expression signatures of Aundiff fractions enriched in self-renewing and differentiation-primed cells. Based on this data and single cell analysis, we characterize Aundiff heterogeneity and identify a population within the GFRα1+ self-renewing pool marked by transcription factor PDX1 plus embryonic patterning genes. We find that PDX1 selectively marks a mature Aundiff population with potent transplantation capabilities and demonstrate an instructive role for niche factors in regulating interconversion between PDX1+ and PDX1− Aundiff. Our studies indicate that Aundiff exist in a series of functionally distinct interconvertible states differentially stabilized through niche interactions.
Generation of a Plzf reporter marking Aundiff
Gene expression patterns characterizing Aundiff subsets remain poorly defined due to lack of markers allowing efficient Aundiff isolation. To develop a system for Aundiff purification, we generated transgenic mice expressing mCherry plus tamoxifen-regulated Cre from regulatory elements of Plzf (Plzf-mC/CreER) (Supplementary Fig. 1a)19,20,21. Immunofluorescence (IF) of testis sections demonstrated that PLZF+ spermatogonia were marked with mCherry in adults from two founders (Fig. 1a and Supplementary Fig. 1b). Similar to endogenous Plzf20, mCherry was prominent in Aundiff and differentiating type-A spermatogonia, identified according to expression of Plzf and Kit plus seminiferous epithelium cycle stage (Fig. 1a, b)22. mCherry was also detected in c-KIT+ spermatogonia at late differentiation stages (In/B) in which endogenous Plzf is downregulated (Fig. 1b). Increased stability of mCherry vs. PLZF or omission of regulatory elements in the transgene may account for this discrepancy. Analysis of fixed, permeabilized testis cells by flow cytometry demonstrated that ~90% of Aundiff (PLZF+ c-KIT−) and essentially all early differentiating cells (PLZF+ c-KIT+) expressed Plzf-mC/CreER (Fig. 1c and Supplementary Fig. 1c). Plzf-mC/CreER is an effective marker of undifferentiated and differentiating spermatogonia.
To confirm that Plzf-mC/CreER is expressed in stem cells, we crossed mice with a transgenic line expressing GFP upon Cre-mediated recombination (Z/EG)25. Tamoxifen (TAM) treatment of Plzf-mC/CreER; Z/EG adults induced GFP in mCherry+ spermatogonia within the epithelium basal layer by day 3 post-treatment (D3) (Fig. 1d, e). Some spermatocytes with low mCherry expression were also GFP+ . At later timepoints, GFP was expressed by mature spermatocytes then spermatids as progeny of transgene-expressing cells differentiated. The majority of tubule cross-sections contained GFP+ spermatogonia D90 after TAM (71.8% ± 1.06, n = 4 testes) (Fig. 1e). Given renewal of the seminiferous epithelium (one round of spermatogenesis takes ~35 days), retention of lineage-marked cells demonstrated that Plzf-mC/CreER was active in stem cells. Whole-mount IF demonstrated that GFP was induced and maintained in a substantial fraction of GFRα1+ As and Apr, consistent with stem cell expression (Fig. 1f)10. By flow cytometry ~50% of Aundiff (PLZF+ c-KIT−) were lineage-marked over the time course, indicating transgene activity in a stable self-renewing population (Fig. 1g and Supplementary Fig. 1d). Early differentiating cells (PLZF+ c-KIT+) labelled more efficiently than Aundiff at initial time points, reflecting prominent transgene expression in these cells (Fig. 1c), progression of marked cells to later differentiation stages and generation of new differentiating cohorts by labelled Aundiff.
To isolate Aundiff from germ cells marked by Plzf-mC/CreER, we stained cells for CD9 and c-KIT, markers of stem and differentiating spermatogonia, respectively3,26. CD9 is also expressed by somatic cells but selection according to CD9 and Plzf-mC/CreER was predicted to allow Aundiff isolation while excluding somatic contaminants. mCherry+ cells could be divided into three fractions: CD9+ c-KIT− (#1), CD9+ c-KIT+ (#2) and CD9low c-KIT− (#3) (Fig. 1h). Subset #1 expresses Aundiff markers (Plzf, Sall4) and markers of stem (Gfra1) and progenitor (Ngn3, Sox3, Lin28a) cells and corresponds to the Aundiff population (Fig. 1i). Subset #2 expresses Kit and Stra8, suggesting it contains differentiating spermatogonia and early spermatocytes3,27. Cells in fraction #3 were presumably mature spermatocytes that contained low mCherry levels (Fig. 1a, b). Selection of cells with high mCherry excluded population #3 while #1 and #2 contained cells with a range of mCherry expression (Supplementary Fig. 1e). Aundiff could not be isolated using CD9 and c-KIT alone due to contamination with Plzf-mC/CreER− somatic cells (Supplementary Fig. 1f).
To confirm identity and purity of this putative Aundiff fraction, we analysed gene expression of population #1 at a single cell level by qRT-PCR (Fig. 1j). 150 out of 152 cells were positive for expression of Plzf and germ cell marker Vasa, indicating somatic cell exclusion and Aundiff enrichment. These cells homogenously expressed Sall4 while Kit expression was limited to few cells. Stem cell-associated genes Gfra1, Etv5, Bcl6b and Id4 exhibited bimodal expression, consistent with heterogeneous expression in Aundiff. Progenitor-associated genes Sox3 and Rarg also displayed bimodal expression patterns. The ability to generate stable clusters of cells in vitro was essentially limited to fraction #1 and cultured cells expressed PLZF, GFRα1 and mCherry, resembling Aundiff (Fig. 1k and Supplementary Fig. 1g)20. Cultured cells upregulated c-KIT plus STRA8 and downregulated Aundiff markers in response to RA, confirming differentiation competence (Fig. 1k and Supplementary Fig. 1g)24. Cultures generated colonies upon transplantation, confirming stem cell activity (Fig. 1l). Through development of a Plzf reporter, we therefore established a system for Aundiff isolation.
Pluripotency reporters exhibit distinct expression in adult Aundiff
To isolate functionally distinct Aundiff and characterize heterogeneity, we developed compound reporter mice with Plzf-mC/CreER, which is expressed throughout the Aundiff pool, and GFP-based reporters marking discrete subsets. Pluripotency gene reporters are associated with stem cell activity and potentially exhibit heterogeneous expression within Aundiff28,29. Sox2GFP marks transplantable testis cells and lineage-marked cells of Sox2CreER adults generate long-lived clones, demonstrating stem cell expression28. Restriction of Sox2GFP expression to isolated spermatogonia in sections suggested that Sox2GFP marks As and short Aundiff28. However, whole-mount IF demonstrated that Plzf-mC/CreER and Sox2GFP were co-expressed throughout the Aundiff pool and in c-KIT+ differentiating spermatogonia (Fig. 2a). Oct4 reporters mark transplantable cells in neonatal testis, suggesting expression in stem cells30,31. The transgene here is based on a 18 kb Oct4 gene fragment lacking proximal enhancer sequences and displays heterogeneous expression in cultured Aundiff29,32. Whole-mount IF of adult Plzf-mC/CreER; Oct4-GFP tubules indicated that Oct4-GFP expression was limited to a subset of Plzf-mC/CreER+ spermatogonia (Fig. 2b). Surprisingly, while Oct4-GFP was expressed in A-type differentiating spermatogonia and Aal, it was generally absent from Plzf-mC/CreER+ As and Apr (Fig. 2b). Analysis of Aundiff by intracellular staining and flow cytometry confirmed heterogeneous Oct4-GFP expression (Fig. 2c). ~40% of PLZF+ c-KIT− Aundiff and ~90% of PLZF+ c-KIT+ were Oct4-GFP+ (Fig. 2d), revealing a correlation between Oct4-GFP and differentiation.
In agreement with these results, GFRα1+ As and Apr (steady-state stem cells10) were generally Oct4-GFP− (Fig. 2e, f). In contrast, most SOX3+ progenitors (including Aal and A1/A2) were Oct4-GFP+ (Fig. 2e, f). We confirmed that Oct4-GFP was preferentially expressed in SOX3+ progenitors vs. GFRα1+ Aundiff at all stages of the epithelium cycle (Supplementary Fig. 2a,b). Oct4-GFP expression positively correlated with spermatogonial chain length in both populations (Supplementary Fig. 2c). By comparison to markers of progenitors (RARγ, LIN28A) and differentiating cells (DNMT3A, CCND1)3,20, we confirmed that Oct4-GFP was expressed in Aal and differentiating A-type cells and downregulated at later differentiation stages (Fig. 2f, g).
Gonocytes of postnatal day 2 (PND2) testes were Oct4-GFP+ as anticipated, confirming transgene integrity (Supplementary Fig. 2d)32. By PND5 Oct4-GFP was heterogeneously expressed in PLZF+ spermatogonia and GFRα1+ cells had lower Oct4-GFP expression than GFRα1− cells suggesting that Oct4-GFP expression is suppressed as gonocytes migrate into the niche. OCT4 protein was restricted to Oct4-GFP+ cells in the neonate (Supplementary Fig. 2d), indicating that Oct4-GFP recapitulates aspects of endogenous Oct4 expression.
To test function of Oct4-GFP+ and Oct4-GFP− Aundiff, cells from Oct4-GFP; Plzf-mC/CreER adults were transplanted and mCherry+ colonies scored after 8 weeks (Fig. 2h). While stem cell activity was significantly enriched within the Oct4-GFP− Aundiff fraction as expected, the Oct4-GFP+ population also contained transplantation activity (Fig. 2i). Oct4-GFP therefore delineates Aundiff populations with distinct characteristics and stem cell activity but transplantation capability is not restricted to the Oct4-GFP− population9,13.
Gene expression signatures of stem and progenitor Aundiff
To gain insight into Aundiff heterogeneity we performed gene expression profiling of Oct4-GFP− and GFP+ Aundiff (Fig. 3a and Supplementary Data 1). From a panel of differentially expressed genes selected according to potential relevance for stem cell function, we confirmed gene expression signatures of Oct4-GFP− and GFP+ Aundiff by qRT-PCR (Fig. 3b). Oct4-GFP+ Aundiff expressed progenitor markers (Ngn3, Rarg, Nanos3, Sohlh1, Lin28a, Stra8, Sox3) at a higher level than Oct4-GFP− Aundiff. Genes downstream GDNF and/or linked with stem cell function (Lhx1, T, Egr2, Etv5, Nanos2, Gfra1, Ret) were enriched in Oct4-GFP− cells16,33. Expression of stem cell marker Id4 was modestly although not significantly enriched in GFP− Aundiff (not shown). Control genes Plzf and Vasa were comparably expressed (Fig. 3b). These data support the observed expression pattern of Oct4-GFP in Aundiff and reveal gene signatures associated with stem and differentiation-primed (progenitor) fractions. Genes associated with pluripotency and embryonic germ cells were co-enriched with Oct4 in the GFP+ progenitor fraction (Dppa2, Dppa3, Gdf3, Lin28a, Prdm14, Tdh, Utf1) (Fig. 3b and Supplementary Data 1). Expression of multiple developmental and cell regulators (Eomes, Lhx1, Pdx1, Smad6, T, Tcl1) were enriched within the GFP− fraction.
To confirm heterogeneous expression of genes from our screen, we analysed candidates plus known Aundiff and germ cell markers by single cell qRT-PCR of Aundiff from Plzf-mC/CreER adults. Data were processed with viSNE, which plots cells in a two-dimensional map where proximity of cell points indicates gene expression similarity34. Projection of expression of a gene of interest in colour allows visualization of cell subsets marked by that gene (Fig. 3c and Supplementary Fig. 2e). Spermatogonia with highest expression of stem cell-associated genes including Gfra1 grouped top right of the viSNE map while cells with highest expression of progenitor-associated genes including Rarg and Sox3 clustered at the opposing end. Cells in between these two groups co-expressed select stem and progenitor genes suggesting they represented transitional states. Expression of genes broadly active in Aundiff (Plzf, Sall4, Vasa) was found throughout the plot (Fig. 3d). While expression of stem cell genes Bcl6b and Id4 was most evident within the stem cell fraction, they were detected in progenitors (Fig. 3d). Pax7 was expressed sporadically (Fig. 3d)35. Expression of differentiation markers Kit and Stra8 was detected, particularly in transitional cells (Fig. 3d).
Heterogeneity was apparent within the Gfra1+ stem cell population; expression of Etv5 and Lhx2 overlapped extensively with Gfra1, while some appeared restricted to a subset. Developmental regulators Eomes, Pdx1, T and Lhx1 marked a subset of Gfra1-expressing cells at one extremity of the viSNE map furthest from progenitors, indicating that gene expression was distinct (Fig. 3c).
Unexpectedly, Oct4 expression was present throughout the viSNE plot, contrasting with restricted expression of Oct4-GFP in progenitors (Supplementary Fig. 2e). The Oct4-GFP reporter marks Oct4 expression in the embryonic germline but lacks specific enhancer elements and is randomly integrated32. Effects of integration site on transgene activity or regulatory roles of omitted enhancers might underlie differences in Oct4-GFP and Oct4 expression. However, expression of Oct4 and other pluripotency genes were similarly enriched in Oct4-GFP+ Aundiff, supporting reporter validity (Fig. 3b). Differences in analysis methods, reporter mouse backgrounds or expression of Oct4 elements retained in the Oct4-GFP reporter may underlie these discrepancies32.
To confirm expression of genes of interest including Oct4 at a single cell level, we isolated Aundiff from Plzf-mC/CreER; Oct4-GFP mice for single-cell RNA-Seq. Data were processed using Monocle to organize cells in a predicted developmental trajectory (pseudotime) according to transcriptional similarities36. After quality controls we identified ~3500 germ cells. Trajectory calculations were performed in semi-supervised mode using expression of genes associated with stem (Gfra1, Etv5) and progenitor (Sox3, Upp1) populations (Fig. 3c) to identify the developmental pathway. A trajectory was obtained from cells only expressing one or both stem markers to those only expressing one or both progenitor markers (Fig. 3e). Transitional cells were defined as expressing combinations of stem and progenitor markers and were distributed along the trajectory with tendency to concentrate mid-trajectory (Fig. 3e). A minor population not identified as stem or progenitor cells according to these markers were “undefined undifferentiated”. Expression of progenitor genes Ngn3 and Rarg increased as cells progressed along the trajectory, indicating that it recapitulated stem to progenitor transition (Fig. 3f). Oct4 expression increased at late pseudotime in agreement with Oct4-GFP expression in progenitors (Fig. 3f). Stra8 expression increased mid-pseudotime, confirming transient induction upon stem cell commitment (Fig. 3d, f). Expression of developmental regulators Eomes, Lhx1 and Pdx1 was limited to initial trajectory stages, consistent with stem cell expression (Fig. 3c, g). T expression was below the set detection level. Id4 was expressed throughout the trajectory but with increased levels at early points indicating preferential but not exclusive stem cell expression (Fig. 3d, g). Other stem cell-associated genes expressed in early trajectory were confirmed, e.g., Nefm, Smad6 and Tcl1 (Fig. 3h). Examination of differentially expressed genes along the trajectory revealed three clusters corresponding to genes downregulated (stem cell-associated), upregulated (progenitor-related) or transiently upregulated across pseudotime (Supplementary Fig. 3). This latter cluster included cell cycle-related genes potentially involved in stem-progenitor transition. We therefore define gene expression signatures of distinct Aundiff populations and dynamics of gene expression during stem-to-progenitor conversion.
Identification of a unique Aundiff population
Single cell analysis revealed a subset of Aundiff within the GFRα1+ self-renewing pool that co-expressed Pdx1, Eomes, T and Lhx1. To confirm existence of this population, we assessed Pdx1 expression in adults by whole-mount IF (Fig. 4a). Pdx1 encodes a homeodomain transcription factor with roles in pancreas development37. Nuclear PDX1 was observed in SALL4+ DNMT3A− isolated spermatogonia and two cell-chains, indicating expression in As and Apr. Flow cytometry of fixed and permeabilized testis cells demonstrated that PDX1+ cells represent a minor fraction (~15%) of PLZF+ spermatogonia and are c-KIT−, confirming Aundiff identity (Supplementary Fig. 4a, b). PDX1+ cells were present at all stages of the seminiferous epithelium and a proportion was KI67+ suggesting that PDX1 does not mark Aundiff with unique mitotic status (Fig. 4a and Supplementary Fig. 4c)2. Consistent with single cell data, PDX1 was restricted to a subset of GFRα1+ Aundiff (Fig. 4a). ~30-40% of GFRα1+ As and Apr were PDX1+ while GFRα1+ Aal were typically PDX1− (Fig. 4b). PDX1+ cells were Oct4-GFP− (Fig. 4a). In testis from Pdx1GFP adults38, GFP was detected in PDX1+ As and Apr, demonstrating antibody specificity (Fig. 4a and Supplementary Fig. 4d). Importantly, the Plzf-mC/CreER reporter was active in PDX1+ cells in a lineage-tracing setting (Fig. 4c).
We next sought to confirm additional markers of PDX1+ Aundiff. While LHX1 and T antibodies performed inadequately, we detected the T-box transcription factor EOMES in ~50% of GFRα1+ spermatogonia in adult testis sections (Fig. 4d and Supplementary Fig. 4e). By flow cytometry, EOMES+ cells were within the PLZF+ c-KIT− Aundiff fraction and comprised ~15% of PLZF+ spermatogonia (Supplementary Fig. 4f, g). EOMES+ cells were Oct4-GFP− and lineage-marked in Plzf-mC/CreER; Z/EG mice upon TAM (Fig. 4e and Supplementary Fig. 4h). Flow cytometry confirmed that PDX1+ and EOMES+ cells were only present within the Oct4-GFP− fraction of the PLZF+ population (Fig. 4f). While PDX1+ spermatogonia were frequently EOMES+, Pdx1 and Eomes expression did not overlap completely; ~60-65% of PDX1+ cells were EOMES+ and vice versa (Fig. 4g, h). That PDX1 and EOMES delineated overlapping but distinct populations was evident from mitotic status. While percentage of PDX1+ cells positive for proliferation marker KI67 was similar to the bulk Aundiff pool, a higher proportion of EOMES+ cells were KI67+ (Fig. 4i, j). Both cell types were present throughout the seminiferous epithelium cycle but found more frequently at early stages (Supplementary Fig. 4i). Moreover, both populations localised preferentially to tubule regions adjacent to the interstitium (Fig. 4k, l)39.
To confirm the immature nature of PDX1+ and EOMES+ Aundiff we assessed expression of stem cell marker Id4 in this population using Id4IRES-GFP mice5,40. Id4 reporter expression in adults was prominent in spermatocytes plus spermatids and marked occasional spermatogonia (Fig. 4m and Supplementary Fig. 4j). While most GFP+ cells were PLZF− c-KIT− by flow cytometry (spermatocytes and spermatids) a subset were PLZF+ c-KIT− (Aundiff) (Supplementary Fig. 4k). Approximately 30% of PLZF+ spermatogonia expressed Id4IRES-GFP (Supplementary Fig. 4l, m). Spermatogonia co-expressing Pdx1, Eomes and Id4 were observed in sections but not all ID4+ spermatogonia were PDX1+ or EOMES+ (Fig. 4m and Supplementary Fig. 4j). By flow cytometry, essentially all PDX1+ and EOMES+ cells were ID4+ but only ~45% of ID4+ spermatogonia were PDX1+ or EOMES+ (Fig. 4n, o), confirming more widespread expression of Id4 than reported5. Combined, we identify Id4-expressing Aundiff marked by PDX1 and EOMES within the GFRα1+ stem cell pool.
Functional and molecular features of PDX1+ spermatogonia
Pdx1 expression is detected in GFRα1+ As and Apr, suggesting it marks stem cells. To test function of PDX1+ cells, GFP+ and GFP− Aundiff from Pdx1GFP; Plzf-mC/CreER mice were transplanted and mCherry+ colonies scored 8 weeks later. A small subset of mCherry+ CD9+ c-KIT− Aundiff was GFP+ (Fig. 5a). While both GFP+ and GFP− fractions generated colonies, PDX1+ cells exhibited significantly higher colony-forming activity than PDX1− Aundiff (Fig. 5b, c). Stem cell potential is therefore substantially enriched in but not exclusive to the PDX1+ population. Colony size from PDX1+ and PDX1− fractions was comparable (Fig. 5d), indicating that PDX1+ and PDX1− stem cells are equipotent. Equivalent GFP+ populations were found in colonies from both fractions, demonstrating that PDX1− Aundiff generate PDX1+ cells upon transplantation and vice versa (Fig. 5b, e).
To define molecular features of PDX1+ cells, we isolated GFP+ and GFP− Aundiff from Pdx1GFP; Plzf-mC/CreER adults for RNA-Seq. Expression of stem cell-associated genes identified from previous analysis (Fig. 3b), including Egr2, Eomes, Etv5, Gfra1, Lhx1, Lhx2, Pdx1, Smad6, T and Tcl1 were enriched in the PDX1+ population (Fig. 5f). Genes associated with progenitors including Dppa3, Esr1, Lin28a, Ngn3, Rarg, Sohlh1, Sox3, Sox10 and Upp1 were expressed at higher levels in PDX1− cells (Fig. 5f). Control genes Plzf, Sall4, and Vasa were comparably expressed while Id4 was expressed at a higher level in PDX1+ cells. Wnt pathway inhibitor Shisa6 was enriched in the PDX1+ fraction41. Oct4 was not differentially expressed between PDX1+ and PDX1− fractions, consistent with discrepancies between endogenous Oct4 and Oct4-GFP expression.
KEGG pathway analysis was performed on genes differentially expressed between PDX1+ and PDX1− Aundiff (Supplementary Data 2). Significant pathways included protein synthesis (ribosome, ribosome biogenesis), metabolism (OXPHOS) and cellular signalling (MAPK and NOTCH pathways) (Supplementary Fig. 5a). PDX1+ cells expressed lower levels of ribosome subunits than PDX1− Aundiff (Supplementary Fig. 5b), consistent with a need to limit protein synthesis rates42. MAPK pathway components (Map2k2/Mek2, Map3k3/Mekk3, Mapk9/Jnk2 and Mapk11/p38b) plus MAPK regulators (Hras, Nf1, Dusp2, Dusp4, Dusp5, Dusp6 and Dusp7) were differentially expressed in PDX1+ and PDX1− Aundiff (Fig. 5g), suggesting a central role for this pathway in Aundiff regulation15,43.
The Pdx1GFP reporter disrupts Pdx1 expression due to GFP insertion38. Pdx1 loss is fatal due to defective pancreas development, so the reporter was maintained in heterozygosity44. Given reported haploinsufficiency of Pdx145 and reduced Pdx1 expression in Pdx1GFP/+ Aundiff (Fig. 5h and Supplementary Fig. 5c, d), we assessed whether germline maintenance was disrupted in Pdx1GFP/+ adults. No disruptions to PLZF+ and differentiating c-KIT+ populations were evident in aged Pdx1GFP/+ mice (Fig. 5i and Supplementary Fig. 5e). Expression of stem cell-associated genes Eomes and Gfra1 in Aundiff from Pdx1GFP/+ adults was not perturbed (Fig. 5h). PDX1 therefore marks Aundiff with unique molecular features and potent stem cell capabilities but reduction in Pdx1 expression does not compromise stem cell function.
Niche factors control transitions between Aundiff states
To examine hierarchy of Aundiff fractions and mechanisms controlling fate, we used our compound reporter models and culture system. When stem and progenitor-enriched Aundiff fractions were isolated from Plzf-mC/CreER; Oct4-GFP adults according to GFP and placed in culture, comparable numbers of cell clusters were formed (Fig. 6a, b). Cultures derived from Oct4-GFP− and GFP+ Aundiff had similar growth rates (Fig. 6c). Established lines were positive for Aundiff markers (PLZF, SALL4, GFRα1) plus mCherry and expressed Oct4-GFP heterogeneously (Fig. 6a). Our data suggested that cultures can be initiated from self-renewing and differentiation-primed Aundiff and cells readily interconvert between stem and progenitor states in vitro (Fig. 2i). Cultures from both sources generated colonies upon transplantation, confirming stem cell capacity (Fig. 6d and Supplementary Fig. 6a).
To confirm dynamics of Aundiff interconversion, sorted Oct4-GFP− and GFP+ cells from established lines were plated at defined density and GFP expression monitored (Fig. 6e). The majority of Oct4-GFP+ cells transitioned into a GFP− state within 1 week but GFP+ cells accumulated at later points. Oct4-GFP− cells generated GFP+ populations over a 2-week period. Adoption of a GFP+ state correlated with increasing culture density (Supplementary Fig. 6b).
Gene expression signatures of freshly isolated Oct4-GFP− and GFP+ Aundiff were mostly retained in fractions from cultures, indicating that Oct4-GFP marks similar populations in vitro and in vivo (Fig. 6f). Importantly, expression of stem cell-associated markers Egr2, Eomes, Etv5, Lhx2, Pdx1 and T were enriched in Oct4-GFP− cells in vitro. However, Lhx1 became evenly expressed between Oct4-GFP− and GFP+ fractions in culture (Fig. 6f). To confirm abundance of Aundiff fractions during culture, we compared Pdx1 and Oct4-GFP expression upon passaging (Fig. 6g). Cell clusters formed from both stem and progenitor-enriched Aundiff fractions contained PDX1+ and Oct4-GFP+ cells. Pdx1 and Oct4-GFP expression were mutually exclusive and Eomes expression mirrored that of Pdx1 (Supplementary Fig. 6c). Oct4-GFP+ cells dominated upon passaging while PDX1+ and EOMES+ cells became relatively rare (Fig. 6g and Supplementary Fig. 6c).
As cultures are founded at clonal density then passaged at higher densities, we hypothesized that declining abundance of PDX1+ and EOMES+ cells upon passaging was due to high-density culture. When plated at low density, established cultures contained prominent PDX1+ and EOMES+ populations and reduced numbers of Oct4-GFP+ cells while increasing density caused accumulation of Oct4-GFP+ cells and reduced PDX1+ and EOMES+ populations (Fig. 6h and Supplementary Fig. 6d). Importantly, GDNF was more rapidly exhausted from media of cells cultured at high vs. low density and increasing GDNF and bFGF levels reduced abundance of Oct4-GFP+ cells and c-KIT+ differentiating populations (Fig. 6i, j and Supplementary Fig. 6e).
These data suggested an instructive role for niche factors in promoting stem vs. progenitor cell states. As GDNF and bFGF regulate self-renewal via distinct pathways46, we assessed importance of each factor in maintenance of the stem cell state. From sorted Oct4-GFP+ cells of established cultures, GDNF promoted adoption of an Oct4-GFP− state while bFGF did not (Fig. 6k). Conversely, the Oct4-GFP− state of sorted cells was lost when bFGF alone was present but maintained with GDNF (Fig. 6k). Cell growth under single factor conditions was more limited than with both factors (Supplementary Fig. 6f). When maintained with bFGF alone, cultures contained more c-KIT+ cells, consistent with switch to a differentiation-primed state (Supplementary Fig. 6g). GDNF thus plays a dominant role in supporting the stem cell fraction. Cell clusters formed with GDNF alone contained more PDX1+ cells than those in media containing bFGF alone (Fig. 6l). When in an appropriate environment, Aundiff therefore reversibly transition between progenitor and stem cell states. Interconversion between discrete states is regulated by niche factors.
Consistent with the role of ERK MAPK downstream GDNF in vivo43, treatment with a MAPK pathway inhibitor depleted PDX1+ and EOMES+ populations in low-density cultures and increased Oct4-GFP expression (Fig. 6m and Supplementary Fig. 6h, i). Inhibitors to PI3Kinase and mTOR, both linked to Aundiff differentiation43,47,48, promoted generation of EOMES+ cells and suppressed proliferation as indicated by KI67 (Fig. 6m and Supplementary Fig. 6i). Effects of PI3Kinase and mTOR inhibitors on PDX1+ populations were less pronounced (Fig. 6m and Supplementary Fig. 6i), suggesting that regulatory inputs to these genes are distinct.
PDX1 and EOMES define distinct stem cell states
The nascent stem cell population is formed during the first postnatal week of testis development and expands dramatically until steady-state spermatogenesis is established49,50. PDX1+ cells were not found in neonatal testis (PND5) and were most evident in adults (Fig. 7a). Occasional PDX1+ cells were observed at PND10 but significant populations not present until PND20. In contrast, EOMES was detectable in subsets of GFRα1+ spermatogonia at PND10 and PND20 (Fig. 7b and Supplementary Fig. 7a). At PND10, EOMES+ cells were generally PDX1− although some were PDX1low. EOMES+ PDX1+ cells became evident by PND20 (Fig. 7b). Distinct developmental timelines for PDX1+ and EOMES+ Aundiff were confirmed by flow cytometry (Fig. 7c, d and Supplementary Fig. 7b, c).
Pdx1 induction coincides with transition from growing to steady-state tissue, indicating that PDX1 marks mature stem cells. Consistent with distinct regulatory inputs, EOMES marks stem cells of developing and mature testis although the proportion of EOMES+ Aundiff increased modestly during development (Fig. 7d). The proportion of Aundiff and EOMES+ cells that were KI67+ declined from PND10 to PND20 and adults consistent with declining mitotic status of stem cells (Supplementary Fig. 7d-f)51. Pdx1 expression did not correlate with Aundiff quiescence (Fig. 4i, j), suggesting that PDX1 is not responsible for lower proliferative rates of mature stem cells.
Male germline cells are depleted by the alkylating agent busulfan. Regeneration of the seminiferous epithelium is reliant on “repopulating stem cells” resistant to genotoxic stress but whether these cells represent a specific Aundiff subset remains unclear52. To test whether PDX1 marks repopulating stem cells, WT mice were treated with a low busulfan dose that depletes differentiating spermatogonia and a substantial Aundiff fraction (Supplementary Fig. 7g-i)4,22. Few spermatogonia one-week after treatment expressed Pdx1, suggesting that PDX1 does not mark busulfan-resistant Aundiff (Supplementary Fig. 7j). By 2 weeks, remaining Aundiff have initiated a regenerative response characterized by long GFRα1+ Aal rarely observed in undisturbed testis (Fig. 7e)4. These Aal were mitotically active as indicated by KI67 but were PDX1−. PDX1+ cells were evident in areas containing GFRα1+ As and Apr but few Aal, which did not appear actively regenerating (Fig. 7e). At 4 weeks, tubule regions contained dense populations of Aundiff and differentiating spermatogonia, indicating successful regeneration (Fig. 7f). PDX1+ populations were found within these areas, consistent with PDX1 marking steady-state stem cells.
Analysis of Aundiff 2 weeks post busulfan by flow cytometry revealed that coincident with increased mitotic activity indicated by KI67, a greater proportion were EOMES+ (Fig. 7g, h). Eomes expression was still restricted to GFRα1+ cells during regeneration (Supplementary Fig. 7k). While most EOMES+ Aundiff express Pdx1 in steady-state testis (Fig. 4h), PDX1 levels in EOMES+ cells under regenerative conditions were reduced (Fig. 7i, j). Accordingly, the proportion of Aundiff expressing Pdx1 was lower than in controls (Fig. 7e, h). Our data suggest that stem cells upregulate Eomes and downregulate Pdx1 under regenerative conditions. Alternatively, EOMES+ Aundiff might be busulfan-resistant and downregulate Pdx1 during regeneration.
To confirm changes in gene expression during development and regeneration, we isolated Aundiff from Plzf-mC/CreER mice at different postnatal ages and 10 days after busulfan for qRT-PCR (Fig. 7k and Supplementary Fig. 7l, m). Across postnatal ages (PND10, 20, adult), expression of stem markers Gfra1 and Id4 were essentially constant while Gfra1 modestly increased after busulfan (Fig. 7k). Pdx1 expression was increased in Aundiff from PND20 and adults compared to PND10 while expression was modestly although not significantly downregulated after busulfan, reflecting persistence of PDX1+ cells in some tubules (Fig. 7e). As anticipated, Eomes expression increased marginally during development but was strongly upregulated after busulfan (Fig. 7k). Other genes marking PDX1/EOMES+ adult Aundiff exhibited distinct dynamics. Lhx1 expression was constant during development but strikingly (~10 fold) increased following busulfan. T expression increased during development but was less responsive to busulfan. Control genes Plzf and Oct4/Pou5f1 were downregulated in adult vs. PND20 Aundiff and reduced following busulfan, suggesting prominent roles in developing rather than steady state or regenerative Aundiff. Changes in Plzf expression were reflected in altered activity of the Plzf-mC/CreER reporter (Supplementary Fig. 7n). Distinct combinations of Eomes, Lhx1, Pdx1 and T expression therefore mark stem cells of developing, homeostatic and regenerating testis.
Aundiff heterogeneity is poorly characterized and cellular hierarchy debated. Taking advantage of compound reporter mice and single cell analysis, we defined gene expression signatures associated with distinct Aundiff populations. We confirmed that Aundiff are broadly divided into GFRα1+ (stem) and RARγ+ (differentiation-primed) fractions10,11. However, gene expression was not homogenous within these populations and we identify a subset of GFRα1+ cells marked by co-expression of Pdx1, Eomes, Lhx1 and T. Heterogeneous T expression within GFRα1+ spermatogonia is reported but functional relevance incompletely understood41. We demonstrated by transplantation that PDX1+ cells have significantly enhanced stem cell activity compared to remaining Aundiff but that stem cells are not exclusive to this fraction. Moreover, in vivo and in vitro evidence indicates that Aundiff reversibly transition between these discrete populations and implicate niche factors in regulation of such transitions. Pdx1 induction within Aundiff coincided with testis maturity while other genes marking adult PDX1+ cells, e.g., Eomes, were expressed during testis development. Further, Pdx1, Lhx1 and Eomes displayed distinct expression dynamics during regeneration. We therefore propose a revised model of Aundiff hierarchy, whereby adult Aundiff exist in a series of dynamic interconvertible states that variably express Pdx1, Eomes, Lhx1, Gfra1 and Oct4-GFP and have distinct functional characteristics (Fig. 7l). Aundiff states are stabilized through interactions with a cognate niche, the property of which varies during development, regeneration and upon tissue homeostasis. Niche status dictates whether specific states, e.g., PDX1+, are sustained. Assignment of Aundiff to these distinct states would affect the balance between self-renewal and differentiation plus functional activity of the Aundiff compartment. Replenishment of cells in the differentiation-primed state and restoration of self-renewing fractions after genotoxic damage is possible via dynamic interconversion of Aundiff states.
Our data argue against strict hierarchical organization of Aundiff fractions akin to that for ID4+ and ID4− Aundiff53. Id4 also appears more broadly expressed in Aundiff than proposed5, complicating interpretation of this model. Oct4-GFP+ PDX1− EOMES− progenitor fractions readily generate Oct4-GFP− PDX1+ EOMES+ cells upon culture and Oct4-GFP+ Aundiff transplant and generate GFP− Aundiff despite minimal Oct4-GFP expression within the GFRα1+ self-renewing pool. Similarly, PDX1− Aundiff generate transplantation colonies containing PDX1+ cells. Our data is consistent with a dynamic stem cell compartment in which Aundiff exhibit context-dependent stem cell activity4. The frequency of cellular transitions under physiological conditions needs to be considered. Oct4-GFP marks GFRα1− SOX3+ RARγ+ Aal, cells that co-express Ngn3 and are differentiation-destined in undisturbed testis19,21. This fate is dictated by RA sensitivity and periodic RA pulses11. Differentiation commitment is also associated with Aundiff eviction from the niche39. Placing differentiation-primed Aundiff in an in vitro environment lacking exogenous RA and containing supraphysiological levels of niche factors can be predicted to restore a self-renewing state. Endogenous stem cell depletion in transplantation recipients permits access of differentiation-primed cells to the niche and an environment promoting self-renewal. Such settings are however unable to rescue self-renewal capacity once Aundiff differentiate54. Our observations highlight a limitation of the transplant assay; Aundiff destined to differentiate in undisturbed tissue still generate colonies in a transplant setting9,13. Lineage tracing provides better insight into cell fate in vivo but also suffers limitations55.
Interconversion of distinct states within the GFRα1+ pool evidently occurs in vivo. Formation of PDX1+ Aundiff, presumably from GFRα1+ PDX1− cells, is observed during postnatal development. Transplanted PDX1− Aundiff generate PDX1+ cells, mimicking this developmental transition. Upon germline recovery following busulfan, the PDX1+ population is restored, potentially from GFRα1+ EOMES+ cells. GFRα1+ cells may routinely transit through distinct states even in steady state while Oct4-GFP+ progenitors must be removed from their physiological context to revert efficiently to a self-renewing state. Lineage tracing studies, e.g., of the GFRα1+ PDX1− population, will be needed to confirm cellular transitions in situ.
Comparison of the male germline with other high-turnover tissues, e.g., haematopoietic, can provide insight into stem cell characteristics in developing and homeostatic settings. Haematopoietic stem cells (HSCs) of the foetal mouse are more mitotically active than adult counterparts and have higher self-renewal capacity56. A switch in murine HSC activity occurs 3–4 weeks postnatally, accompanied by changes in gene expression and differentiation potential57. Self-renewal mechanisms of foetal and adult HSCs are distinct and postnatal transition in HSC properties regulated through intrinsic cues58,59. While transplantable stem cells are present in early postnatal testis onwards, age-dependent changes in Aundiff properties and self-renewal mechanisms are poorly appreciated. Our data indicate that common to HSCs, Aundiff are more mitotically active in neonates than adults. Transplantation studies demonstrated that stem cells from pups have altered proliferative capacities and differentiation tendencies than those of adults51. Pdx1 is induced in a population of As and Apr in young adults that possess potent transplantation capabilities, suggesting that PDX1 marks the onset of a mature stem cell phenotype. After germ cell depletion by busulfan, Pdx1 is downregulated in regenerating Aundiff and PDX1+ populations only recover upon epithelium renewal. Similar demands are likely placed on stem cells in developing and regenerating tissues, i.e., founder/remaining stem cells expand rapidly to establish/restore the stem cell compartment then generate differentiating cells. Loss of PDX1+ Aundiff during regeneration is consistent with development of this population in homeostatic testis. It will be of great interest to characterize phenotypic and functional differences between Aundiff under homeostatic vs. developmental or regenerative conditions and factors responsible for divergent properties.
Given that PDX1+ Aundiff development coincides with maturation of supporting Sertoli cells and GDNF promotes adoption of a PDX1+ cell state in vitro60, extrinsic cues can drive formation of this population. Genes sharing similarly restricted expression as Pdx1 in adult Aundiff (Lhx1, Eomes, T) are positively regulated by GDNF in cultured Aundiff, supportive of a role for this niche factor16,33. However, GDNF levels peak in early postnatal testis and are induced following busulfan-mediated germ cell depletion14,61, conditions in which PDX1+ cells are not found. The presence of high bFGF levels in addition to GDNF may promote Aundiff expansion under these conditions but prevent adoption of the PDX1+ state62. EOMES+ Aundiff are present during postnatal development and enriched in regenerative testis, consistent with GDNF-dependent regulation. Whether conserved signals regulate Pdx1 expression in foregut tissues and postnatal testis remains to be determined. Selective induction of genes such as Pdx1 in adult stem cells indicates that besides neonatal gonocyte-to-spermatogonia transition, stem cell formation involves an additional developmental step occurring upon exposure of nascent Aundiff to a mature testis environment.
Mouse generation and manipulation
The Plzf-mC/CreER transgenic reporter line was generated at the Monash Gene Targeting Facility through standard pro-nuclear injection techniques. Recombineering was used to construct the transgene from a BAC template. The mCherry-T2A-CreERT2 cassette replaces the second exon after the translation initiation site and is followed by a poly(A) sequence. The transgene incorporates 20 kb upstream Plzf, the first untranslated exon and first intron plus 1 kb of the second intron. Two independent founder lines were established and mice from the first line were used for the majority of experiments. Z/EG, Sox2GFP, Oct4-GFP, Pdx1GFP and Id4IRES-GFP lines have been described elsewhere25,28,32,38,40. Hemizygous or heterozygous reporter mice were generally maintained on a mixed C57BL6/CBA background except Oct4-GFP (C57BL6/CBA/129T2svJ) and Id4IRES-GFP (FVBN/CBA) lines. For lineage tracing, Plzf-mC/CreER; Z/EG mice (4–6 weeks old) were injected intraperitoneally daily with 2 mg tamoxifen (Sigma-Aldrich) in sesame oil for 5 consecutive days22. Wild-type mice for analysis of testis development and regeneration were C57BL6. Adult mice were generally harvested at 8–10 weeks of age. Busulfan (Cayman Chemical) was prepared for intraperitoneal injection as described22. Spermatogonial transplantation was performed using busulfan-conditioned C57BL6/CBA F1 recipients20. A volume of 10–15 μl of donor cell suspension was microinjected via the testis efferent ducts. Recipients of cells from Oct4-GFP mice were treated with neutralising antibody to CD4 to promote immune tolerance35,63. All animal experiments were subject to approval by the Monash University Animal Ethics Committee.
For frozen sections, testes were harvested and fixed in 4% paraformaldehyde (PFA) overnight at 4 °C then washed in phosphate-buffered saline (PBS) prior to cryoprotection with 30% sucrose in PBS and embedding in OCT. Sections (8 μm) were processed as previously detailed20 and blocked with 10% foetal bovine serum (FBS) or donkey serum with 2% bovine serum albumin (BSA) in PBS. Whole-mount immunostaining of seminiferous tubules is described elsewhere48. For immunostaining of cultured Aundiff, cells were plated onto Lab-Tek II chamber slides (Thermo Fisher Scientific) coated with Geltrex (Thermo Fisher Scientific) and allowed to form colonies. Cells were fixed in 4% PFA for 10 min at room temperature and washed in PBS prior to permeabilization for 10–15 min in methanol at −20 °C. Slides were blocked and stained as for sections above. Primary antibodies were as follows: Goat anti-GFRα1 (AF560, 1:250), anti-c-KIT (AF1356, 1:250), anti-mouse/rat PDX1 (AF2517, 1:250), anti-PLZF (AF2944, 1:500), anti-LIN28A (AF3757, 1:500) and anti-SOX3 (AF2569, 1:250) (R&D Systems), rabbit anti-mCherry (ab167453, 1:2000), anti-OCT4 (ab19857, 1:500), anti-SALL4 (ab29112, 1:2000) (Abcam), chicken anti-GFP (ab13970, 1:5000) and rat anti-germ cell-specific antigen (TRA98, 1:500) (Abcam), rat monoclonal anti-mCherry clone 16D7 (Thermo Fisher Scientific, 1:2000), rabbit monoclonal anti-Cyclin D1 clone SP4 (1:250) and mouse monoclonal anti-DNMT3A clone 64B1446 (1:200) (Novus Biologicals), rat anti-KI67 clone SolA15 (eBioscience, 1:250), rabbit monoclonal anti-c-KIT clone D13A2 (1:400) and anti-RARγ clone D3A4 (1:500) (Cell Signaling Technology) and rabbit monoclonal anti-mouse EOMES clone 1219A (R&D Systems, 1:1000). Primary antibodies were detected with appropriate Alexa Fluor-conjugated secondary antibodies (Thermo Fisher Scientific and Jackson ImmunoResearch, 1:500) and samples counterstained with DAPI prior to mounting with Vectashield mounting medium (Vector Labs). Samples were analysed on a Zeiss LSM 780 confocal microscope (Monash Micro Imaging).
To generate single-cell suspensions from adult testis, dissected seminiferous tubules were coarsely minced and washed with PBS then digested with 1 mg/ml collagenase Type IV (Sigma-Aldrich) in unsupplemented DMEM medium and 50 μg/ml DNase I. Tubule fragments were washed in PBS to deplete interstitial cells and peritubular myoid cells then dissociated with 0.25% trypsin in the presence of DNase I and passed through a 70 μm cell strainer. For live analysis and sorting, cells were stained with FITC (1:250) or biotin-conjugated (1:500) anti-CD9 clones KMC8 or MZ3 (eBioscience and Biolegend) and allophycocyanin (APC)-conjugated anti-c-KIT clone 2B8 (eBioscience, 1:500). Biotinylated antibody was detected with streptavidin conjugated to APC-eFluor 780 (eBioscience, 1:2000) and DAPI used for live/dead discrimination. Spermatogonia-enriched fractions for sorting were prepared by CD9 selection using an EasySep biotin selection kit (Stem Cell Technologies) and biotinylated CD9 antibody (Biolegend clone MZ3, 1:500) according to manufacturers instructions. For intracellular staining, testis cell suspensions were fixed in PFA then permeabilized in methanol on ice for 30 min or overnight at −20 °C. Fixed and permeabilized cells were washed in PBS with 2% FBS then stained with the following antibodies: chicken anti-GFP (Abcam ab13970, 1:5000), eFluor 450-conjugated anti-Ki67 clone SolA15 (1:500) and phycoerythrin (PE)-conjugated anti-c-KIT clone 2B8 (1:250) (eBioscience), rabbit polyclonal anti-mCherry (Abcam ab167453, 1:1000), goat anti-mouse/rat PDX1 (R&D Systems, AF2517, 1:300), rabbit anti-mouse EOMES clone 1219A (R&D Systems, 1:1000) and Alexa 647-conjugated anti-PLZF clone 9E12 (1:2000)20. Antibodies to EOMES, GFP, mCherry and PDX1 were detected with Alexa 488 and 568 conjugated secondary antibodies (Thermo Fisher Scientific and Jackson ImmunoResearch, 1:500). Cells were analysed on an LSR Fortessa and sorted with a BD Influx Cell Sorter (BD Biosciences). Data were processed with FlowJo software.
Aundiff cultures were established and maintained on mitomycin-inactivated mouse embryonic fibroblast (MEF) feeders in StemPro-34 media (Thermo Fisher Scientific) supplemented with 10 ng/ml GDNF, 10 ng/ml bFGF, 20 ng/ml EGF, 25 μg/ml insulin and other additives as described20,64. Cultures between passages (P) 3 and 8 were used unless indicated otherwise and harvested using Trypsin/EDTA. For analysis of cell growth and GFP expression by flow cytometry, cells were plated onto 24-well plates at indicated densities and followed over time. When analysed by flow cytometry, Aundiff were distinguished from contaminating feeders by mCherry expression. For IF, cells were plated onto four-well chamber slides coated with Geltrex (Thermo) as detailed22. GDNF levels in conditioned media from cells cultured on 12-well plates were measured with a DuoSet ELISA system (R&D Systems). To induce differentiation, cells were treated with 1 μm retinoic acid in DMSO (Sigma-Aldrich) for 48 h. For transplantation, cells were dissociated with Trypsin/EDTA and resuspended at 5 × 106 cells/ml in germ cell media supplemented with 50 μg/ml DNase I and 10% Trypan blue (Sigma-Aldrich). Inhibitors to MAPK (PD0325901; 5 μm), PI3Kα (BYL719; 1 μm) and mTOR (Torin; 0.5 μm) (Selleckchem) were dissolved in DMSO then diluted in media. Inhibitor-containing media was replaced each day for 4 days prior to cell analysis.
Microarray and qRT-PCR
Sorted cells were lysed in TRIzol LS reagent (Thermo Fisher Scientific) then RNA was purified and DNase treated using a Direct-zol RNA Miniprep kit (Zymo Research). Gene expression in Aundiff fractions from pooled Oct4-GFP; Plzf-mC/CreER mice (three independent sorts) was analysed with an Agilent Technologies SurePrint G3 8 × 60 K microarray at the Monash Health Translation Precinct Genomics Facility. Significance was determined by paired t test (P < 0.05) with 1.5-fold change cutoff. For qRT-PCR, cDNA was synthesized from isolated RNA using a Tetro cDNA synthesis kit (Bioline). Quantitative PCRs were run on a Roche LightCycler 480 using Takara Sybr Premix Ex Taq II (Clontech). Primer sequences were as previously described20,23 or obtained from the Harvard PCR Primer Bank (https://pga.mgh.harvard.edu/primerbank/) and listed in Supplementary Table 1.
RNA was purified from sorted cells and DNase treated using a Direct-zol RNA Microprep kit (Zymo Research). RNA quality and quantity was assessed using a Bioanalyser and Qubit. SPIA amplification and cDNA generation was performed using 2 ng total RNA as per Nugen Ovation RNA-seq system V2 protocol followed by Ovation Ultralow System V2 for library preparation. SPIA amplified cDNA was quantitated and 100 ng sheared using Covaris sonication and processed. Seven cycles of amplification were used to minimize any amplification effects. Library size (~320 bp) was checked by Bioanalyzer. Libraries were quantified by Qubit and qPCR and one equimolar pool made based upon qPCR results. Following denaturation, 200 pM of library pool was clustered in one lane of a HiSeq 3000 8-lane flowcell using c-Bot. RNA-sequencing was performed at the Medical Genomics Facility, Monash Health Translation Precinct (MHTP). Data was processed by the Monash University Bioinformatics Platform using the RNAsik pipeline. Raw reads (FASTQ) were mapped against Ensembl reference files (FASTA and GTF) followed by read counting. Differential gene expression was performed with Degust webtool, based around the R package limma using limma-voom for statistical analysis. Differentially expressed genes were classified using the DAVID Bioinformatics Resource and KEGG pathway database65.
Preamplified template for single cell PCR was generated with Fluidigm’s C1 platform as per instrument specifications. In two independent experiments a total of 152 mCherry+ CD9+ c-KIT− cells isolated from pooled Plzf-mC/CreER adult testis were captured and preamplified with 71 TaqMan probes to the following genes (those identified as differentially expressed in Oct4-GFP+ and GFP− Aundiff fractions by microarray are underlined): Actb, Bcl6b, Ccnd2, Ccne1, Cd82, Cxcr4, Ddit4, Ddx4, Dmrt1, Dnmt3a, Dnmt3b, Dnmt3l, Dppa2, Dppa3, Egr2, Eif4b, Elk3, Eomes, Esr1, Etv1, Etv4, Etv5, Fbxw7, Fgfr1, Fgfr2, Foxo6, Gfi1, Gfra1, Hprt, Id4, Ifitm1, Ifitm3, Itga6, Itgb1, Kit, Lhx1, Lhx2, Lin28a, Myc, Nanos2, Nanos3, Neurod1, Ngn3, Notch1, Pax7, Pdx1, Pou3f1, Pou3f2, Pou5f1, Rarg, Ret, Rpl32, Rspo1, Sall1, Sall4, Six2, Smad6, Snai1, Sohlh1, Sox2, Sox3, Sox10, Stra8, T, Tbx20, Tcl1, Tet3, Thy1, Upp1, Zbtb16 and Zic2. Single-cell PCR data collection was performed with a Biomark instrument (Fluidgm). Results are expressed as Log2Ex = LOD (Limit of Detection) Cq − Cq [Gene]. The limit of detection was set to 28. If Log2Ex value is negative, Log2Ex = 0. Summary statistics and plots were performed and produced using made4, caroline and gplots66,67. viSNE, a visualization tool for high-dimensional single-cell data based on the Barnes-Hut implementation of the t-Distributed Stochastic Neighbour Embedding (t-SNE) algorithm was applied to the data set34. In detail, 0.1 was added to Log2Ex values and resulting tables converted to flow cytometry standard files. The Cytobank platform (Fluidgm, South San Francisco, California) was used for generation of viSNE maps.
mCherry+ CD9+ c-KIT− Aundiff fractions were independently isolated from 2 Plzf-mC/CreER; Oct4-GFP adults and resuspended at ~300 viable cells/μl in PBS containing 0.04% BSA. Library construction was performed using a 10 × Chromium controller with the Chromium Single Cell 3′ Reagent Kit V2. Both libraries were sequenced in one high-output lane of an Illumina NextSeq in single-read 150b format (115b effective read length). Single-cell (sc) RNA-seq processing and analysis was performed with Cell Ranger software (10× Genomics, Inc.) and Monocle36,68,69. scRNA-seq samples were demultiplexed with cellranger mkfastq. Sequencing reads were aligned to a custom mouse genome (Cell Ranger mm10 version 1.2.0, including GFP and mCherry sequences as extra chromosomes). The annotation file was modified to count reads assigned to both GFP and mCherry cassettes and UMIs counted with cellranger count. Both libraries were aggregated and normalized by depth, to have the same of number of mapped reads, with cellranger aggr. Gene expression matrix, containing both cell and expression details, were processed for downstream analysis using both cellRanger’s load_cellranger_matrix and Monocle’s newCellDataSet function (lowerDetectioLimit = 0.5 and expressionFamily = negbinomial.size()).
Analysis was performed using components of Monocle’s package unless otherwise stated. Cell counts were normalised with the estimateSizeFactors function previously discarding mitochondrial and ribosomal associated genes70. Cell gene expression was detected using detectGenes (min_expr = 0.1) and genes not expressed in at least 175 cells were discarded. Dispersion was estimated for the remaining gene set using estimateDispersions70. Cells with a total number of mRNA (log10) within two standard deviations from the mean were kept for further analysis.
In a first instance, cell classification was performed with classifyCells based on the following criteria: contaminant cells were defined as those cells that expressed at least one transcript of Acta2, Icam2 or Cdh5 marker genes; germ cells were those cells that expressed at least one transcript of Zbtb16, Ddx4 or Sall4 and did not express any of the contaminant cell marker genes. Only those cells classified as germ cell were used for downstream analyses. Cells with no detectable expression of the housekeeping gene Gapdh (senescent) were also excluded from the analysis.
For single-cell trajectory analysis, germ cells were ordered in a semi-supervised mode using a cell type classification based on the following criteria: transitional cells were defined as those cells that express at least one transcript of both stem (Etv5 and Gfra1) and progenitor (Upp1 and Sox3) marker genes; stem cells were defined as those cells that expressed at least one transcript of the stem cell marker genes but did not express progenitor marker genes; progenitor cells were defined as cells that expressed at least one transcript of the defined progenitor marker genes and did not express stem cell marker genes. A minor fraction of cells was not classified as either stem or progenitor cells based on the described markers and were referred to as undefined undifferentiated. The makerDiffTable function (residualModelFormulaStr = “~Library+ num_genes_expressed”) was used to identify those genes that were co-expressed with markers that define cell type hierarchy described above (top 2500 genes based on q value were selected as ordering genes). Dimensionality reduction was performed with reduceDimension using the discriminative dimensionality reduction with trees (DDRTree) method and log normalization. Cells were ordered along the trajectory with orderCells (reverse = T). Differential gene expression test along the cell trajectory was performed with differentialGeneTest (fullModelFormulaStr = “~sm.ns(Pseudotime)+ Library+ num_genes_expressed” and reducedModelFormulaStr = “~Library+ num_genes_expressed”). Cell trajectory, gene expression across pseudotime and heatmap of pseudotime plots were created with plot_cell_trajectory, plot_genes_in_pseudotime (min_expr = 0.1, trend_formula = “~ sm.ns(Pseudotime, df = 4)”) and plot_pseuodtime_heatmap respectively.
Assessment of statistical significance was performed using a two-tailed unpaired t-test (GraphPad Prism). P-values are indicated as follows: *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001; not significant (ns) P > 0.05. For mouse experiments, no statistical method was used to predetermine sample sizes and no specific randomization or blinding methods were used.
Microarray and RNA-Seq data are deposited in the Gene Expression Omnibus (GEO) database as a SuperSeries with accession number GSE107256. All other relevant data are available from the corresponding author on request.
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We thank Jeanette Rientjes and Jose Gonzalez of the Monash Gene Targeting Facility for generating the Plzf-mC/CreER transgenic line and technicians of the Monash Animal Research Platform for animal care. We would also like to thank Patrick Western, Anand Hardikar, Jane Visvader and Alex Swarbrick for supplying reporter mice. We are very grateful to Antonella Papa for helpful discussions and comments plus Marco Seandel for advice on spermatogonial transplantation. We acknowledge the facilities, scientific and technical assistance of Monash Micro Imaging, FlowCore and Micromon of Monash University. This work was supported by an Australian Research Council (ARC) Future Fellowship to R.M.H. and by the Stem Cells Australia ARC Special Research Initiative. J.M. was supported by a fellowship from the Sigrid Jusélius Foundation. J.M.P. is a Viertel Senior Medical Research Fellow. The Australian Regenerative Medicine Institute is supported by grants from the State Government of Victoria and the Australian Government.