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In adult skin, epithelial hair follicle stem cells (SCs) reside in a quiescent niche and are essential for cyclic bouts of hair growth. Niche architecture becomes pronounced postnatally at the start of the first hair cycle. Whether SCs exist or function earlier is unknown. Here we show that quiescent cells appear early in skin development, express SC markers, and later give rise to the adult SC population. To test whether early quiescent cells function as SCs, we use Sox9-Cre for genetic marking and K14-Cre to embryonically ablate Sox9, an essential adult SC gene. We find that the progeny of Sox9-expressing cells contribute to all skin epithelial lineages and Sox9 is required for SC specification. In the absence of early SCs, hair follicle and sebaceous gland morphogenesis is blocked and epidermal wound repair is compromised. These findings establish the existence of early hair follicle SCs and reveal their physiological importance in tissue morphogenesis.
Adult stem cells (SCs) maintain tissues during normal homeostasis and wound repair. SCs frequently reside in specific niches which provide the appropriate microenvironment and molecular cues to preserve proliferative and tissue regenerative potential, the hallmarks of SCs (Blanpain and Fuchs, 2006; Moore and Lemischka, 2006). In mammalian hair follicles (HFs), SCs reside in a relatively quiescent state within a permanent, anatomically distinct region of the follicle known as the bulge. In adult mice, bulge SCs can contribute to all three epithelial lineages of skin (Blanpain et al., 2004; Morris et al., 2004; Oshima et al., 2001). During normal homeostasis, bulge SCs are periodically activated to fuel postnatal hair cycles. While the interfollicular epidermis (IFE) and sebaceous gland (SG) both contain resident populations of unipotent progenitor cells, multipotent bulge SCs can provide a cellular input to both of these lineages in a wound environment.
While all HFs have initiated development by P0 when mice are born, bulge niche architecture is not pronounced until three weeks after birth (~P20-P21) when mice already have a full hair coat (Cotsarelis, 2006; Schmidt-Ullrich and Paus, 2005). The distinctive appearance of the bulge at this age coincides with the onset of the growth phase (anagen) of the first postnatal hair cycle. Where the adult bulge SCs come from and how they organize within a niche remains unknown. It has been widely assumed that bulge SCs are not needed for embryonic morphogenesis, where HFs develop from epidermis rather than the base of preexisting bulge niches. In support of this notion, two widely used bulge SC markers, CD34 and a keratin 15-LacZ reporter gene, are both upregulated at ~P20 (Blanpain et al., 2004; Liu et al., 2003; Trempus et al., 2003). Additionally, while many studies using postnatal nucleotide tracer pulse-chase experiments have demonstrated the quiescence of adult bulge SCs (Cotsarelis et al., 1990; Morris and Potten, 1999; Taylor et al., 2000), the existence of a quiescent cell population within developing HFs has never been reported.
The isolation and transcriptional profiling of bulge SCs has revealed many new markers that offer additional insights into the characteristics and behavior of follicle SCs. Among the upregulated bulge genes are transcription factors Lhx2, Sox9, Tcf3 and Nfatc1 (Blanpain et al., 2004; Morris et al., 2004; Trempus et al., 2003; Tumbar et al., 2004). Interestingly and in contrast to CD34, their expression begins early in HF morphogenesis, with Lhx2 and Sox9 appearing at the placode stage and Tcf3 and Nfatc1 appearing later during the peg stage (Horsley et al., 2008; Nguyen et al., 2006; Rhee et al., 2006; Vidal et al., 2005). While null mutations in all four genes cause embryonic lethality, skin grafts from Lhx2 and Nfatc1 null embryos develop HFs which contain functional SC niches but display reduced SC quiescence (Horsley et al., 2008; Rhee et al., 2006). Y10:Cre/Sox9(fl/fl) mice target Sox9 ablation to postnatal skin, revealing hair cycle defects that include a failure of adult bulge SCs to form and/or express CD34 (Vidal et al., 2005).
Despite the importance of these adult follicle SC transcription factors and their expression in embryonic skin, it is not known whether these genes function during morphogenesis. It is similarly unclear how and when the SC niche is established, an issue that is poorly understood for most tissues harboring stem cells. In this report, we use a combination of genetics, cell biology and in vivo functional assays to investigate the specification and initial function of epithelial SCs in the hair follicle. We find that these SCs are specified during the earliest stages of HF morphogenesis and that initial SC specification critically depends on Sox9. Furthermore, we find that early SCs can contribute to all three skin epithelial lineages and in their absence, the normal morphogenesis of HFs and SGs is blocked and epidermal wound repair is severely compromised.
In order to determine when the quiescent bulge SC population is first specified, we modified in vivo pulse-chase experiments previously employed for labeling adult bulge cells with histone H2B-GFP (Tumbar et al., 2004). Similar to our previous strategy, we used K5-Tetoff mice to control keratin 5 (K5)-positive skin epithelial expression of histone H2B-GFP driven by a tetracycline regulatable enhancer, but in this case, we began our chase at embryonic day 18.5 (E18.5). At this early time, most hair follicles have been specified, but are still in the early stages of morphogenesis.
In unchased embryos, all skin epithelial cells displayed H2B-GFP epifluorescence, consistent with strong K5 promoter activity by E13.5 (Fig. 1A). After 3d of chase (P2), the brightest H2B-GFP cells in the epidermis were in non-proliferative suprabasal layers, as expected from the upward mode of terminal differentiation in this tissue. Surprisingly, the brightest cells in the hair follicle were concentrated in a relatively narrow zone (bracketed) of outer root sheath (ORS). After 9d of chase when HF downgrowth was nearly complete (P8), H2B-GFP label retaining cells (LRCs) clustered prominently within this upper ORS zone. Marking completion of the pilosebaceous unit (Schmidt-Ullrich and Paus, 2005), SGs had emerged just above these LRCs (Fig. 1A).
Consistent with their relatively slow-cycling nature, these early follicle LRCs were largely negative for proliferative nuclear protein Ki67, which instead marked many cells located both above (infundibulum) and below (matrix) this zone (Fig. 1A). In mature follicles, a thin trail of H2B-GFP-positive cells (arrowheads) extended down the ORS from the concentrated LRC zone towards the hair bulb, which contains the highly proliferative, transit-amplifying population of matrix cells responsible for hair production. Intriguingly, some of the cells within this trail displayed decreased nuclear epifluorescence intensity and some were also negative for Ki67, suggestive of a potential precursor-product relation between brighter H2B-GFP LRCS in the upper ORS and dimmer H2B-GFP cells in the lower ORS.
Use of fluorescence activated cell sorting (FACS) to quantify label retention in keratinocytes from fractionated epidermis or HFs (dermis) revealed that unchased HF keratinocytes expressed relatively uniform amounts of label at E18.5 but after 3d of chase, the spectrum of GFP fluorescence had broadened, indicating that most HF keratinocytes had divided several times (Figure S1A). Over 4d of chase, the HF GFP spectrum continued to broaden and diminish in intensity, reflecting rapid cell divisions. That said, a clear tail of GFP-high cells persisted, indicative of a less proliferative subset of HF cells. The variable rates of HF cell division contrasted starkly with the more uniform epidermal cell division rates reflected by symmetric distributions of label retention (Figure S1A).
To determine whether early LRCs might be related to adult follicle SCs, we conducted immunofluorescence microscopy with antibodies against a number of adult bulge markers and compared their localization patterns with H2B-GFP (Fig. 1B). Consistent with prior reports (Nguyen et al., 2006; Vidal et al., 2005), transcription factors Tcf3 and Sox9 were expressed in P8 ORS. While not restricted to H2B-GFP LRCs, Tcf3 and Sox9 positive cells included the LRC zone (brackets). Notably, Nfatc1 and Lhx2 were also expressed in the LRC zone and displayed even greater restriction than Tcf3 and Sox9 (arrowheads). Whether embryonic or adult, the only other place where Nfatc1, Lhx2 and LRCs are known to co-localize is in adult bulge SCs (Horsley et al., 2008; Rhee et al., 2006; Tumbar et al., 2004).
To directly evaluate the relation between early follicle LRCs and adult bulge SCs, we labeled mice until E18.5 and then chased until P21, when the first postnatal hair cycle is initiated (Blanpain et al., 2004). After an entire cycle of hair growth, LRCs marked by H2B-GFP during embryogenesis were still present at P21 where they localized to the CD34-positive adult bulge SC niche and secondary hair germ (HG) (Figure 1C). This result, confirmed by FACS analysis on 22d chased mice (Figure S1B), established that the early LRC population present in chased P3 and P9 follicles is the major contributor to the adult bulge SCs that appear at P20-21.
Taken together, these results demonstrate that a quiescent population of cells is specified early in HF development, that LRCs localize to a specific region of the growing HF where they express many SC markers, and that early LRCs persist to form the adult bulge. Notably, all of these quiescent, presumptive bulge cells lost some label during a 22d chase that covered the first complete hair cycle, leading us to postulate that these cells play an active role in HF morphogenesis before being called upon to drive the periodic growth of the adult hair cycle.
To determine whether early LRCs might be important for HF morphogenesis, we traced expression of the known SC markers that we found to co-localize with these cells. Of the four bulge transcription factors, only Lhx2 and Sox9 were known to be expressed in the early hair placodes (Rhee et al., 2006; Vidal et al., 2005). We focused on Sox9 as a particularly good candidate for regulating LRC establishment during embryogenesis, since fortuitous postnatal HF targeting of Sox9(fl/fl) mice with a Y10:Cre transgene had resulted in adult HFs that lacked CD34 and which could not be maintained (Vidal et al., 2005).
In WT E14.5 embryos, the skin was marked by uniform E-cadherin expression and Sox9 protein was not present (Figure 2A). As predicted from the pattern of Sox9 in situ hybridization (Vidal et al., 2005), Sox9 protein marked developing placodes as soon as they could be architecturally discerned in the main waves of HF specification (E15.5-P0). Interestingly and unexpectedly, however, nuclear Sox9 protein resided in the suprabasal cells of the placode rather than in the P-cadherin and Lhx2 positive basal layer (Figure 2B). No previous studies on genes or signaling pathways have uncovered the existence of this unique Sox9-positive cell population within the placode.
By the peg stage, Sox9-expressing cells concentrated in a region in the upper ORS with moderate P-cadherin expression, while the brightest PCad-positive cells localized to the leading edge of developing follicles (Figure 1C). Once sebaceous glands (SG) emerged, it was clear that this Sox9-expressing ORS zone encompassed the presumptive bulge region (Figure 2D). By P2, a trail of Sox9-positive cells extended down the ORS, diminishing towards the matrix which was negative for Sox9. As previously reported (Vidal et al., 2005), the bulge SCs of adult HFs were positive for Sox9 (Figure 2E). Real time PCR on FACS-purified skin cells revealed background levels of Sox9 mRNA expression in all populations besides ORS, validating the accuracy of our Sox9 immunofluorescence results (Figure 2F).
Given the similarity between Sox9 expression and LRC location in developing HFs, we wondered whether Sox9-expressing cells in embryonic skin might actively contribute to HF morphogenesis. To test this possibility, we conducted a genetic marking analysis using Sox9-Cre/R26R skin. In this assay, Sox9-Cre expressing cells become permanently marked for LacZ expression, and all progeny of Sox9-Cre expressing cells can then be readily monitored over time by β-galactosidase cleavage of XGal to generate a blue dye.
Although some portions of backskin express Sox9-Cre as early as E10.5 (Akiyama et al., 2005), tailskin, which is similar to backskin (Braun et al., 2003), was free of Sox9-Cre activity prior to HF development. At E18.5, tailskin XGal reactivity paralleled Sox9 immunolabeling, specifically marking cells in the upper portion of developing HFs, but remaining absent from the leading edge of HFs and the IFE (Figure 2G). By P8, however, HFs were almost entirely blue, demonstrating that the population of Sox9-expressing cells in the upper ORS had contributed not only to all differentiated layers of the growing HF but also the SG. By the first telogen (P21), Sox9-derived progeny encompassed most if not all cells of the HF, including those of the infundibulum, SG, bulge and secondary hair germ, but were absent from IFE (Figure 2G).
In normal homeostasis, a resident unipotent progenitor population within the IFE maintains skin turnover. In response to wounding, however, adult bulge SCs can be recruited to the IFE to assist in repair (Ito et al., 2005; Claudinot et al., 2005; Levy et al., 2007). Interestingly in P3 Sox9-Cre/R26R mice, scratch wounding resulted in a robust contribution of Sox9-Cre marked HF cells into the regenerating IFE (Figure 2G). Taken together, these studies revealed that Sox9-expressing cells within developing skin display key properties of adult HF stem cells in that they contribute to HF and SG morphogenesis and can repair an injured IFE.
In conditionally targeted Y10:Cre/Sox9(fl/fl) mice, HFs produced an atrophic hair coat that was retained into adulthood, thereby directing that study to a role for Sox9 in the adult hair cycle (Vidal et al., 2005). In light of our finding that a Sox9-marked bulge may form during skin embryogenesis, however, we were intrigued that hair defects had been noted in Y10:Cre Sox9 mice as early as P8 (Vidal et al., 2005). To directly test whether Sox9 is functionally required for skin morphogenesis, we targeted Sox9 ablation using K14-Cre, active in skin by E13.5. At E16.5, when many follicles are present only as placodes, the Sox9 locus had been efficiently targeted (Figures S2, 3A). At birth, K14-Cre/Sox9(fl/fl) (cKO) mice were phenotypically distinguished from WT by an 80% reduction in whisker number, and at P6, when the hair coat first appears, cKO mice displayed a smooth epidermal surface with no sign of protruding hairs. As cKO mice aged, they remained completely devoid of a hair coat (Figure S2). These findings strongly supported an early role for Sox9.
The effects of Sox9 ablation during embryogenesis appeared to be specific for the early SC population in the presumptive bulge. Thus, despite a morphologically intact, K17-positive ORS, the thickening that normally marks the location of early Sox9-positive bulge cells was missing (Figures S3A, 3B). Moreover, in contrast to WT HFs, where nuclear Nfatc1 marked a few cells within the presumptive bulge, Nfatc1 was never detected in developing cKO skin (Figure 3C, S3B). Additionally, even though Sox9 was absent in cKO hair germs, Lhx2 was still expressed initially in its normal location at the leading edge; however, Lhx2 failed to appear subsequently in the presumptive bulge (Figure 3D). Finally, although Tcf3 was detected initially in the ORS of developing cKO follicles, it was progressively lost during the first week after birth (Figure 3E). Notably, the earliest disappearance of Tcf3 occurred within the presumptive bulge region, and then proceeded unidirectionally towards the follicle base (Figure 3E).
Although establishment of early bulge architecture and gene expression was clearly impaired in developing Sox9-deficient HFs, it remained possible that early bulge cells were still present within the ORS but could no longer be identified by these criteria. Since our studies had shown that early bulge cells reduce their cycling rate as they develop, we conducted an embryonic BrdU pulse-chase to see if early LRCs were also lost when Sox9 was absent. Strikingly, significant differences in the numbers of cKO follicles with LRCs were already evident by P2 and by P6, LRCs were diminished by ~8X fold (Figures 3F, S3C). The dramatic reduction in LRCs in the presumptive bulge of Sox9-deficient neonatal HFs was accompanied by a substantial increase in proliferation in this zone. A 6 hr pulse of BrdU at P6 revealed an increase of ~40% in BrdU-labeled cells within the total Sox9 cKO upper ORS population, mostly concentrated in the region of the presumptive bulge (Figure 3G). Similar differences were observed with proliferation markers Ki67 and G1/S-regulatory kinase Cdk4 (Figure S3D-E).
Our findings unveiled new requirements for Sox9, namely in the early expression and maintenance of transcription factors and slow-cycling bulge SC features which we found to be established during embryogenesis, long before other bulge markers, such as CD34, appear. When taken together with our earlier label-retaining and genetic marking studies, these additional data provided compelling evidence that not only does a population of early bulge stem cells form during skin development, but that its features critically rely upon one of the transcription factors that marks it.
We next addressed our finding that Sox9-dependent early bulge SCs form during HF morphogenesis in the context of the absent hair coat phenotype of Sox9 cKO mice. Histological analysis of skin from our P0 cKO mice revealed no significant differences in overall HF density or developmental stage (Figures 4A, S4A). By contrast, differences in HF length were already evident at P0 and by P6, cKO follicles averaged ~60% the length of WT follicles (Figure 4A). Despite gross perturbations in HF length, overall morphology and biochemical features of HF differentiation were relatively normal, and the ORS, IRS and hair shaft all appeared to be present and correctly organized (Figure S4, B-H). Importantly, K14-Cre targeted Sox9 ablation efficiently prior to the main waves of HF specification and well before differentiated HF lineages developed. Thus, rather than specifying HFs or governing their differentiation, Sox9 appeared to function in maintaining the growth of HFs once morphogenesis was initiated.
To investigate this fascinating possibility further, we returned to Sox9-Cre/R26R mice, this time focusing on the developmental activity of Sox9-expressing cells at the same time points when defects became apparent in Sox9 cKO mice. At P0 and P2, blue cells were detected in the upper ORS (bracketed) (Figure 4B). Notably, the initial matrix was negative for XGal reactivity. By P4 however, a trail of blue cells extended from the ORS into the matrix (Figure 4B, arrowheads). By P7, most matrix cells were blue, and only small patches of negative cells could be detected within the hair bulb (asterisk). Since the matrix was negative for Sox9 mRNA and protein, the progressive expansion of XGal reactivity into these compartments at the expense of unmarked cells implies that during early HF development, Sox9-expressing cells provide an active input to the newly formed matrix, whose initial residents are transient.
To test whether the loss of early bulge SCs in Sox9 cKO mice might result in an early failure to maintain the transit-amplifying matrix population, we next analyzed matrix size over time. No differences were noted at P0, suggesting that initial specification of matrix was unimpaired in the absence of early SCs (Figure 4C). However, in contrast to WT matrix, which gradually expanded from P0 to P10, Sox9 cKO matrix only transiently expanded until P2 before it began to shrink and nearly disappear by P10 (Figure 4C). Concomitant with the loss of Ki67-positive matrix cells was an abrupt change in dermal papilla morphology (Figure S5), commensurate with that known to occur upon exit of HFs from the growth phase of the hair cycle (Stenn and Paus, 2001). Moreover, Sox9 cKO HFs failed to proceed through any further stages of the hair cycle at later timepoints, consistent with the requirement of HF SCs in driving hair cycle progression (data not shown) and with the absence of a hair coat in our mice.
Direct evidence for a decreased input of SCs to the matrix in Sox9 cKO HFs was provided by a series of short BrdU pulse chase experiments which allowed us to distinguish possible causes of a smaller matrix population, including precocious differentiation, decreased proliferation or impaired input of SCs to the matrix. At all times, the percentage of BrdU-positive cells per bulb was similar, suggesting that cKO cells proliferate at the same rate as WT cells (Figures 4D, S6A). Additionally, only minor differences in differentiation rate were detected, suggesting that the relative balance of proliferation and differentiation was largely unimpaired (Figures 4D, S6A). The cKO HFs were also generally free of apoptotic cells, suggesting that cell death was not a major cause of smaller matrix size (Figure S7). Strikingly, however, cKO HFs displayed a marked decline in ORS input to the matrix, with an ~33% reduction in the percentage of BrdU-positive cells in the lower ORS at 12h and an ~50% reduction at 20h (Figures 4D, S6A).
Based upon these results, the initial cells that formed the matrix and differentiated HF lineages appeared to be transient and not dependent upon Sox9 for their formation. However, without the Sox9-positive early bulge SCs, this pool of transit amplifying matrix cells was not maintained and as a direct consequence, HFs did not progress through the growth phase of the hair cycle.
Although SGs possess their own resident unipotent progenitors marked by Blimp1, adult bulge SCs can differentiate along a sebaceous lineage in a wound environment or when SG progenitors are defective (Blanpain et al., 2004; Horsley et al., 2006; Morris et al., 2004). Based upon our Sox9-Cre marking results and the temporal appearance of early bulge SCs prior to development of SGs, we wondered whether early bulge SCs might be essential for this lineage. Indeed, Blimp1-positive SG progenitors were absent in cKO follicles (Figure 5A). Also missing was PPARγ, a key sebocyte differentiation marker (Figure 5B). Lipid dye (Oil-red O), which normally permits visualization of SG morphology by P6 only stained the subcutaneous adipocytes and revealed no signs of SGs in cKO follicles (Figure 5C).
Our genetic marking experiments using Sox9-Cre mice also provided evidence that HF cells derived from a Sox9-expressing population can contribute to repair of wounded IFE. To test whether Sox9-expressing early bulge SCs might be essential for efficient HF contribution to IFE repair, we conducted engraftment experiments on Nude mouse recipients with split-thickness P0.5 dermis/HF tissue (Figure S8A). Pilot experiments with K14-H2BGFP mice validated the split thickness grafting technique, yielding >90% GFP-positive donor cell IFE reconstitution (Figures S8B, S8C). To distinguish donor from host cell contributions in our Sox9 test grafts, male skins were grafted onto female Nude recipients, and fluorescence in situ hybridizations were performed with a Y chromosome specific probe (Y-FISH).
The data from the engraftments of Sox9 cKO vs WT skins are summarized in Figure 6. Full and split thickness grafts from WT mice displayed comparably thick, uniform hair coats, and quantification of skin surface areas revealed no significant differences. Similarly, although full thickness grafts from Sox9 cKO skin lacked hair and showed a slightly scaly epidermis, the average graft areas were similar to WT. All of these grafts expanded in size over time, indicating their robust nature in growth and ability to repair wounds. Y-FISH revealed that the IFE of all of these grafts was almost completely donor-derived.
While split thickness grafts from cKO skin were initially the same size as the other grafts, they always shrank substantially within a 6 week period and displayed markedly reduced numbers (typically ~15%) of Y-positive IFE cells (Figures 6A,C). The presence of Y-positive dermal cells underlying the Y-negative IFE confirmed the efficacy of the initial grafting procedure, and a delay in IFE regeneration was ruled out by monitoring grafts for up to 16 wk after engraftment (Figures 6B,D), at which time the percentage of Y-positive IFE cells had further decreased. These experiments revealed that, despite their later acquisition of IFE markers (Figure S9), neonatal Sox9 cKO HFs lacking early SCs are severely impaired in their ability to repair damaged IFE.
Since quiescence is a hallmark of cells residing in the adult bulge SC niche (Cotsarelis et al., 1990; Morris and Potten, 1999; Taylor et al., 2000), we reasoned that by determining when and where quiescence is established, we might use this property to identify and characterize an early SC population within HFs and trace the development of adult SCs. Our embryonic pulse-chase studies demonstrated that HF LRCs are specified early in morphogenesis, and begin to accumulate in a specific region of the HF where they express bulge-preferred transcription factors. Although early expression of several of these markers has been noted previously, the physiological significance of their expression at this early time had not been realized nor was it known that their expression correlated with the emergence of a developing niche of LRCs. Our studies place these earlier clues in perspective and firmly establish the existence of a functional niche of multipotent, quiescent SCs within early developing HFs.
Importantly, by extending the chase after embryonic labeling, we demonstrated that early LRCs are the direct precursors of the LRCs that reside in the adult bulge niche. Interestingly, while early LRCs express many of the same transcription factors that adult bulge cells do, they do not express CD34, which has widely been used as a key SC marker (Trempus et al., 2003; Morris et al., 2004; Blanpain et al., 2004). While the physiological significance of CD34 remains unclear, Sox9 has emerged as a key regulator of stem cell identity, marking both early and adult SCs. Sox9 also marks the trail of follicle SCs that appear to migrate from the bulge to the transit amplifying matrix during the HF growth phase.
By taking advantage of Sox9 as a marker of early LRCs, we were able to trace the origins of early bulge SCs to the hair placode. It is intriguing that placodes consist of two populations of cells that can be distinguished by their differential expression of Lhx2 and Sox9, since these two markers are later co-expressed not only by early bulge SCs but also adult bulge SCs. Our Sox9 genetic marking studies suggest that the early basal placode cells that are marked by Lhx2 and P-cadherin are transient. They give rise to the initial hair bulb, but then seem to disappear entirely by ~P7. By contrast, the Sox9-expressing cell population which starts as only a few cells within the suprabasal layer of the placode gives rise not only to the long-lived, self-renewing SCs of the bulge but also the entire pilosebaceous unit, including the infundibulum. Moreover, concomitant with the emergence of Sox9-positive early LRCs is the expression of Lhx2, Nfatc1 and Tcf3 which thereafter continue to identify the multipotent SCs of the HF.
In the adult follicle, the active, cycling portion is thought to originate from bulge SCs (Ito et al., 2004). How and why is a separate transit amplifying population specified during initial HF morphogenesis? While additional experiments will be necessary to fully elucidate the significance of this finding, it is interesting that a developmental paradigm of using separate TA and SC populations during morphogenesis has also been described in blood development, where hemogenic cells drive primitive hematopoiesis before long-term hematopoietic SCs commence definitive hematopoiesis (Orkin and Zon, 2008). Our studies now pave the way for examining expression patterns of other adult SC markers in these two placode residences and should allow us to predict how a given gene might function to control subsequent HF morphogenesis.
The existence of an initial pool of Sox9-independent matrix cells explains why HF morphogenesis and differentiation begin normally in Sox9 cKO embryos. The premature exhaustion of these transient cells in the absence of subsequent input from Sox9-positive SCs further explains why HF maturation and hair production halt midstream during morphogenesis. These findings also demonstrate convincingly that the initial matrix relies upon input from early Sox9-positive SCs for its maturation, and that matrix cells cannot enhance their own self-renewal to compensate for a lack of early bulge SC input.
Some years ago, Oshima et al. (2001) observed that in the anagen phase of the adult rat whisker, bulge cells continue to migrate along the ORS to the hair follicle bulb, where they become matrix cells. Since this initial report, it has been widely debated whether this phenomenon is merely another feature unique to whisker follicles or whether backskin bulge SCs posess similar activity. Our studies on the development of WT and Sox9-deficient backskin follicles not only provide compelling evidence in support of the Oshima studies, but also show that the fueling of the matrix by Sox9-positive bulge cells is functionally required to maintain the matrix.
Another surprising finding that emerged from targeting Sox9 ablation in the embryo was that SGs failed to form, even though Sox9 was not expressed in the SG lineage or its resident progenitors. The dependency of the SG lineage on Sox9-expressing cells was particularly intriguing considering that the emergence of Sox9-marked LRCs occurred just before that of sebaceous glands. Taken together, the inability of HF morphogenesis to proceed without Sox9-positive cells and the failure of SGs to form altogether establishes the early Sox9-expressing population as a multipotent SC pool essential for completing skin morphogenesis. These important conclusions could not be predicted from postnatal ablation of Sox9 in the skin (Vidal et al., 2005), and they provide major new insights into the existence and usage of a follicle stem cell population at a stage and for a purpose that has hitherto been unanticipated.
Although nucleotide double-labeling experiments have detected HF-derived contributions to the IFE of young neonatal mice (Taylor et al., 2000), lineage tracing studies with a Shh-Cre reporter active in the developing placode suggest that the development of HFs and IFE involves distinct progenitors (Levy et al., 2005). Our Sox9-Cre lineage tracing experiments are consistent with Shh-Cre studies in showing that Sox9-Cre marked cells in the HF do not contribute to IFE either during its development or its subsequent homeostasis. However, our studies further revealed that in a wound response, Sox9-Cre marked HF cells in neonatal mice were robustly recruited to repair the IFE. This finding underscored the similarities between early bulge SCs and adult bulge SCs aiding in IFE repair (Ito et al., 2005; Levy et al., 2005; Levy et al., 2007; Tumbar et al., 2004). Our split thickness grafting approach allowed us to further measure the IFE reconstitution efficiency of early bulge SCs in a wound response and in long-term wound repair. Not only did HF-derived progeny repopulate the IFE with close to 100% efficiency, but these cells were also maintained stably over a four month period. Moreover, HFs from Sox9 cKO mice lacking early SCs were highly impaired in regenerating IFE, suggesting that early SCs may be essential in order for follicles to participate in this process.
Our model summarizing the roles of Sox9-dependent early SCs in skin morphogenesis is presented in Figure 7. We've found that a quiescent SC population is formed during the earliest stages of HF morphogenesis and subsequently gives rise to cells in the adult bulge SC niche. This early SC population is essential for normal morphogenesis of both HFs and SGs, and it robustly contributes to the IFE lineage in a wound environment. While we have identified a single gene, Sox9, which is required for early SC specification, our studies now set the foundation for identification of additional molecules and pathways involved in the formation and regulation of these early SCs. A comprehensive understanding of the embryonic origins of SC development is an essential first step not only for normal tissue biology but also for a wide variety of human diseases, including cancers, where SC and/or niche biology is genetically altered.
K14-H2BGFP (Tumbar et al., 2004), BATGal (Maretto et al., 2003) and pTRE-H2BGFP/K5-tetVP16 (Tumbar et al., 2004) mice have been described. Sox9-IRES-Cre mice (Akiyama et al., 2005) were crossed to ROSA26Flox-Stop-Flox-βgeo (R26R) mice (Mao et al., 1999). Sox9flox/flox mice (Akiyama et al., 2002) were crossed with K14-Cre mice (Vasioukhin et al., 1999).
For H2B-GFP pulse-chase experiments, pregnant pTRE-H2BGFP/K5-tetVP16 females with known plug dates were fed continuously with doxycycline chow beginning at E18.5. 5-Bromo-2’-deoxyuridine (BrdU) embryonic pulse-chase experiments were conducted by injecting pregnant females carrying E17.5 embryos with an intraperitoneal (IP) loading dose of 50μg/g BrdU and adding BrdU to drinking water for a 24 hour period at 0.8mg/mL. Postnatal BrdU experiments were conducted by single IP injection of 50μg/g BrdU.
Full thickness grafts from newborn mice were performed as described (Rhee et al., 2006). For split thickness grafts, backskin from P0 mice was placed dermis-side down in 5mM EDTA in PBS for 1 hour at 37°C. The epidermis was then removed as a single sheet from HF/dermis, which was then grafted in the same manner as full thickness grafts. In all cases, paired WT and cKO tissues of identical size were grafted on a single Nude recipient. Bandages were removed 12-14 days after grafting. Graft area was measured using a Canon Powershot S70 camera attached to a dissecting microscope and quantified using ImageJ software and a calibrated standard area.
HF/dermis cells from P0.5-P6 mice were isolated as previously described (Rendl et al., 2005), and epidermal cells were isolated by brief trypsinization of the epidermal sheet removed from full thickness skin after overnight 4°C dispase treatment. Cell isolation from P21 mice and all FACS stainings were performed as previously described (Blanpain et al., 2004). FACS analyses were performed on a FACSCalibur flow cytometer (BD Biosciences) using CellQuest Pro software.
Epidermal cells were collected by trypsinization of either full thickness E16.5 skin, or dispase-separated epidermis from P0.5 and P4 skin. ORS, Mx, DP, DF and Mc populations were prepared as previously described (Rendl et al., 2005). Total RNA was isolated using the Absolutely RNA Kit (Stratagene) and cDNA was synthesized using SuperScript III (Invitrogen). RT-PCR was performed on a LightCycler 480 (Roche) using SYBR Green I master mix. Sox9 mRNA expression levels were expressed as a function of GADPH mRNA.
Skins were embedded in OCT, frozen, sectioned and fixed in 4% paraformaldehyde. Immunofluoresence, XGal staining, hematoxylin/eosin staining, and in situ hybridizations were performed on OCT sections as previously described (Kaufman et al., 2003). Alkaline phosphatase detection of DP and Oil-red O staining of SGs were performed on OCT sections as previously described (Horsley et al., 2006; Rendl et al., 2005). Y-FISH analysis was performed on OCT sections using a Cy3 Star*FISH detection kit (Cambio). For immunohistochemistry, skins were fixed in formaldehyde and then dehydrated and embedded in paraffin. Antigen unmasking was performed using a Retriever 2100 for 20 min (Pick Cell Laboratories BV). Detection of immunohistochemical staining was performed using a Vectastain ABC kit (Vector Laboratories). Student's t-test was used to determine statistical significance.
We especially thank Benoit de Crombrugghe (Baylor U) and Andreas Schedl (INSERM, Nice) for their generosity in providing us with Sox9-Cre and Sox9(fl/fl) mice, respectively. Mice were housed and bred in the LARC ALAAC-accredited animal facility at The Rockefeller University, and we are especially grateful to Nicole Stokes for her technical assistance related to the expert care of these mice. We also thank Danelle Devenport, Valerie Horsley and Rui Yi in the Fuchs’ laboratory for their critical reading of this manuscript, and Horace Rhee for pilot studies on embryonic LRCs. JN is an MD/PhD student supported by NIH MSTP grant GM07739 and partially by NRSA training grant CA09673; EF is an Investigator of the Howard Hughes Medical Institute. This work was supported in part from a grant from the NIH (EF).
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