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PLoS One. 2013; 8(6): e66314.
Published online Jun 18, 2013. doi:  10.1371/journal.pone.0066314
PMCID: PMC3688887
Lgr5 Identifies Progenitor Cells Capable of Taste Bud Regeneration after Injury
Norifumi Takeda,1,2,3*¤ Rajan Jain,1,2,3 Deqiang Li,1,2,3 Li Li,2 Min Min Lu,2 and Jonathan A. Epstein1,2,3*
1Department of Cell and Developmental Biology, Perelman School of Medicine at the University of Pennsylvania, Pennsylvania, United States of America
2Penn Cardiovascular Institute, Perelman School of Medicine at the University of Pennsylvania, Pennsylvania, United States of America
3Institute of Regenerative Medicine, Perelman School of Medicine at the University of Pennsylvania, Pennsylvania, United States of America
Marcello Rota, Editor
Brigham & Women's Hospital - Harvard Medical School, United States of America
* E-mail: notakeda-tky/at/umin.ac.jp (NT); epsteinj/at/upenn.edu (JAE)
Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: NT RJ DL JAE. Performed the experiments: NT MM LL. Analyzed the data: NT RJ DL JAE. Contributed reagents/materials/analysis tools: NT RJ. Wrote the paper: NT RJ JAE.
¤Current address: Department of Cardiovascular Medicine, Graduate School of Medicine at the University of Tokyo, Tokyo, Japan
Received March 8, 2013; Accepted May 4, 2013.
Taste buds are composed of a variety of taste receptor cell types that develop from tongue epithelium and are regularly replenished under normal homeostatic conditions as well as after injury. The characteristics of cells that give rise to regenerating taste buds are poorly understood. Recent studies have suggested that Lgr5 (leucine-rich repeat-containing G-protein coupled receptor 5) identifies taste bud stem cells that contribute to homeostatic regeneration in adult circumvallate and foliate taste papillae, which are located in the posterior region of the tongue. Taste papillae in the adult anterior region of the tongue do not express Lgr5. Here, we confirm and extend these studies by demonstrating that Lgr5 cells give rise to both anterior and posterior taste buds during development, and are capable of regenerating posterior taste buds after injury induced by glossopharyngeal nerve transection.
Taste buds are sensory organs detecting sweet, bitter, sour, salty, and umami (savory), and they are composed of at least three types of fusiform gustatory receptor cells (type I–III) as well as round cells in the basal compartment (type IV). Taste receptor cells in the adult are postmitotic and trophically maintained by the activity of taste neurons. They are a relatively short-lived and heterogeneous population of cells that are continually replaced by progenitor cells, the characteristics of which remain poorly defined [1][3].
Taste buds mature peri-natally within epithelial appendages, termed taste papillae, which arise at mid-gestation as epithelial thickenings or placodes. Recent lineage tracing experiments using inducible Cre-Lox technologies demonstrated that Sonic hedgehog (Shh)-expressing cells in the embryonic placodes are taste receptor cell progenitors, giving rise to mature taste buds in young postnatal animals [4]. However, these derivatives gradually disappear by 4 months of age, suggesting that additional, Shh-, progenitor cells are recruited to replenish the mature taste bud lineages in adult mice. Type IV cells have been proposed as a precursor cell population of taste receptor cells [2], [5], but they include a heterogeneous population that includes Shh and Prox1-expressing cells [6], [7]. In addition, fate-mapping studies of adult type IV cells have not been undertaken to confirm or refute this hypothesis.
There is some evidence suggesting that adult taste buds are derived from the surrounding extragemmal epithelium (i.e. epithelial progenitors extrinsic to the taste bud itself) [8], [9]. For example, cell lineage analysis using an X-linked mosaic transgenic mouse line has suggested that taste buds and the adjacent epithelial cells arise from a common progenitor residing within the local surrounding epithelium [8]. In addition, Keratin 14 (K14)-expressing basal epithelial keratinocytes, genetically labeled using a Cre-Lox strategy, can give rise to taste receptor cells and to tongue epithelium [9]. Indeed, previous studies have suggested that taste papillae epithelial cells immediately surrounding taste buds are distinct from more remote tongue epithelial cells; they express high levels of Sox2 [10] and Shh target genes, Patched (Ptc) and Gli1 [6], [11]. Thus, local surrounding epithelium represents a potential source of mature taste bud stem/progenitor cells, though experimental evidence for this hypothesis remains lacking.
Lgr5 is expressed in stem/progenitor cells of multiple tissues, including the hair follicle and intestinal crypt [12], [13] and functions as a Wnt co-receptor in the β-catenin signaling pathway [14]. Lgr5-expressing cells have recently been shown to give rise to at least some new taste buds during the normal cycles of growth and regression [15]. Although Lgr5 is detected in the tongue epithelium from embryonic stages [16] and Wnt/β-catenin function is necessary and sufficient for taste placode formation [17], [18], the role of Lgr5+ cells during development of taste buds or after injury remains poorly elucidated. Here, we demonstrate that Lgr5+ cells function as progenitor cells for taste buds during development. In addition, we show that Lgr5+ cells can give rise to newly regenerated taste buds in the posterior region of the tongue during normal homeostasis and after injury in adult mice.
Mice
Lgr5EGFP-ERCre/+ [12], ShhERCre/+ [19], R26Tom/+ [20] mice have been described previously. All mice were maintained on mixed genetic backgrounds. The University of Pennsylvania Institutional Animal Care and Use Committee approved all animal protocols (Permit Number; 803396).
Lineage Tracing Experiments
Mice were injected intraperitoneally with tamoxifen (100 mg/kg body weight; Sigma) dissolved in corn oil, as a single dose or daily for 5 consecutive days, as indicated.
Glossopharyngeal Neurectomy (GLx)
Mice were intraperitoneally anesthetized with 2,2,2-tribromoethanol (300 mg/kg body weight; Sigma), and all efforts were made to minimize suffering. An incision was made along the ventral neck midline and the digastric muscle was exposed. The posterior belly of the digastric muscle was retracted, and the glossopharyngeal nerve passing between carotid arteries was transected as it entered the jugular foramen. Bilateral glossopharyngeal nerves were transected because taste buds of the circumvallate papilla are bilaterally innervated.
BrdU Labeling Experiments
In vivo bromodeoxyuridine (BrdU) incorporation was performed to analyze cell proliferation. Mice were subjected to GLx, and 2 days later injected intraperitoneally with BrdU (100 mg/kg; Sigma). Tissues were collected 2 hours after BrdU administration, and then stained with an anti-BrdU monoclonal antibody (Rat, 1[ratio]20, Accurate).
Histology and Microscope
Tongues were fixed in 2% paraformaldehyde, ethanol dehydrated, embedded in paraffin, and sectioned. Antibodies used were: GFP (goat, 1[ratio]100, Abcam), RFP (recognizes tdTomato) (rabbit, 1[ratio]50, Rockland), Ki67 (rabbit, 1[ratio]50, Santa Cruz), PCNA (mouse, 1[ratio]50, Biocare), Sox2 (goat, 1[ratio]10, Santa Cruz) (rabbit, 1[ratio]500, Seven Hills Bioreagents), Phospholipase C, β2 (PLC β2) (goat, 1[ratio]25, Santa Cruz) (rabbit, 1[ratio]2000, Santa Cruz), Carbonic Anhydrase IV (CA4) (goat, 1[ratio]25, R&D systems), Prox1 (rabbit, 1[ratio]50, Abcam), and Cytokeratin 8 (CK8) (rat, 1[ratio]50, Hybridoma Bank). All immunohistochemistry was visualized on a Nikon Eclipse 80 i fluorescence microscope. For stereomicroscope observations, tongues were visualized on an Olympus MVX10 fluorescent dissecting microscope. All images were analyzed using Adobe Photoshop (sizing, brightness or contrast adjustments, etc.). Brightness and contrast was adjusted linearly across the entirety of each image.
Statistics
Data are shown as mean ± SD. Paired data were evaluated using Student’s t-test. P values less than 0.05 were considered statistically significant.
Lgr5 Expression in Taste Papillae
To identify Lgr5 cells in tongue epithelium, we used Lgr5-EGFP-IRES-ERCre knock-in mice (Lgr5EGFP-ERCre/+), which express both EGFP and Cre-ERT2 fusion protein from the endogenous Lgr5 locus [12]. EGFP fluorescence was detected in the region of the developing taste papillae from mid gestation through the first few weeks after birth. However, expression gradually declined and became undetectable from intact tongue specimens by postnatal day 20 (P20) (Fig. 1A–D). Lgr5 was broadly expressed by tongue epithelium at embryonic day 13.5 (E13.5), and expression was greater in the Prox1+ placode than the surrounding tongue epithelium (Fig. 1E, F). Lgr5 was also expressed by the early postnatal fungiform (FG) taste papillae of the anterior tongue. Expression overlapped with that of CK8 and Prox1 in the taste bud and was also evident in the surrounding epithelium (Fig. 1G, H). However, Lgr5 expression was absent in adult mature FG papillae (Fig. 1I).
Figure 1
Figure 1
Lgr5 expression during taste papillae development.
In contrast, Lgr5 expression could be detected in developing circumvallate (CV) and foliate (FL) taste bud papillae of the posterior tongue as well as in adult mature stages (Fig. 1J–N and data not shown). At 0.5 day after birth (P0.5), CV papillae demonstrated shallow epithelial trenches. Lgr5 was expressed within the papillae epithelium as well as CK8+ and Prox1+ immature taste bud cells. However, it was absent from the epithelium surrounding the CV papillae (Fig. 1J–L). As the CV trenches deepened and the number of taste buds increased with age [21], Lgr5 expression gradually decreased and localized to the local epithelium surrounding adult taste buds (Fig. 1M and S1). Expression was most pronounced within the basal epithelium immediately surrounding taste buds (Fig. 1N). Lgr5 expression was also detected within Prox1+ type IV taste bud basal cells (Fig. 1O). Most adult Lgr5+ cells were cycling cells (Ki67+/PCNA+) (Fig. 1P, Q) and coexpressed Sox2 (Fig. 1R), a marker of taste bud progenitors located outside the taste bud itself [9], [10]. These data suggest that Lgr5+ cells have important roles in the development and maintenance of taste buds.
Lgr5 Expression Defines Taste Bud Progenitor Cells
To track the fate of Lgr5+ cells, we crossed Lgr5EGFP-ERCre/+ mice with R26Tom/+ indicator mice [20], in which tdTomato expression can be induced by Cre-mediated recombination. Tamoxifen was injected intraperitoneally to activate Cre-recombinase at two different times: P1 and P50. When Lgr5-expressing cells were labeled at P1, both anterior and posterior taste papillae were labeled 1 month after the treatment, and could still be detected at 5 months (Fig. 2A–F). One month after treatment, 87% (75/86) of labeled FG papillae demonstrated tdTomato expression confined to the taste buds (Fig. 2G), while 13% (11/86) had expression in taste buds and the surrounding epithelium (Fig. 2H). Six months after treatment, all Lgr5-derived FG papillae (n = 7) revealed tdTomato expression within taste buds and the surrounding epithelium (Fig. 2I). This pattern of expression and labeling suggests that long-lived or self-renewing Lgr5+ cells reside in the surrounding epithelium rather than in the taste bud. On the other hand, posterior CV papillae 1 and 5 months after treatment displayed similar tdTomato expression patterns: both taste buds and the surrounding epithelium, including type I (Sox2+), type II (PLC β2+) and type III (CA4+) taste cells, contained derivatives of Lgr5+ cells (Fig 2J–M and S2).
Figure 2
Figure 2
Lineage tracing of neonatal Lgr5 cells.
In a second series of experiments, adult Lgr5EGFP-ERCre/+;R26Tom/+ mice were pulsed with tamoxifen for 5 consecutive days (P50–54). Only posterior taste papillae were labeled, and fated cells remained present 15 months after tamoxifen induction (Fig. 3A–F and data not shown). Lgr5-derivatives were not detected at any time in the FG papillae (Fig. 3G). However, Lgr5-derivatives marked every type of taste receptor cells and surrounding epithelium in posterior taste papillae 15 months after tamoxifen (Fig. 3H–K). No ectopic reporter activity was detected in uninduced control mice (Lgr5EGFP-ERCre/+;R26Tom/+, Fig. S3). Taken together, these results suggest that neonatal Lgr5 expression defines progenitor cell populations in both anterior and posterior taste papillae that can give rise to taste receptor cells and/or the surrounding keratinocytes, while adult Lgr5 expression marks progenitor cells of the posterior taste papillae only.
Figure 3
Figure 3
Lineage tracing of adult Lgr5 cells.
Shh Cells of Adult Taste Papillae are a Transient Precursor of Taste Bud Cells
Adult Shh+ type IV cells have been suggested to be a transient precursor cell population of adult taste buds [2], though this has not been experimentally tested. Therefore, we conducted lineage tracing experiments using adult ShhERCre/+;R26Tom/+ mice (tamoxifen pulse P50–54) [19]. Lgr5 is also expressed by occasional intragemmal type IV cells (Fig. 1O). One month after tamoxifen treatment, Shh-derived cells were evident in most tongue taste papillae (Fig. 4A–C) but disappeared over the subsequent 2 months (Fig. 4D). Shh-derived cells were located only within taste buds but not the surrounding epithelium (Fig. 4E, F), and Shh+ cells gave rise to all taste receptor cell types (Fig. 4G–I). Derivatives could not be detected in any taste papillae 3 months after induction (data not shown). Taste receptor cells are replaced approximately every 8–22 days (depending on the exact cell type) [3] and Lgr5+ cells can contribute to long-term maintenance of taste receptor cells. Therefore, we conclude that the type IV cells marked by Shh-expression are a transient precursor cell population of adult taste buds but not a long-term stem cell population. Rather, long-term maintenance is dependent upon an Lgr5+, Shh- population. Further definition of the heterogeneous population of type IV cells remains to be elucidated. In addition, Lgr5-derived cells mark extragemmal epithelial cells and are not formed from Shh+ cells, suggesting the existence of an extragemmal adult taste bud stem cell niche.
Figure 4
Figure 4
Lineage tracing of adult Shh+ cells.
Lgr5 Cells Participate in Regeneration of Taste Buds
We sought to determine if Lgr5+ cells could reconstitute taste buds after injury. Transection of the glossopharyngeal nerves bilaterally (GLx) results in degeneration of posterior taste papillae followed by regeneration over the ensuing several weeks [2], [22]. We pulsed Lgr5EGFP-ERCre/+;R26Tom/+ mice with tamoxifen at P50–54 and performed GLx 2 weeks later (Fig. S4). Two days after injury, Lgr5 expression and cell proliferation (measured by BrdU incorporation and usually robust in the epithelial compartment) was markedly reduced (Fig. 5A, B). As expected, CK8+ taste bud cells gradually disappeared and were no longer detected by 14 days after GLx (Fig. 5C–E) [22]. Notably, many Lgr5-derivatives within the local epithelium survived GLx-induced injury (Fig. 5E). Regenerated taste buds were apparent four weeks after GLx (Fig. 5F, G and S4), and all three types of taste receptor cells derived from Lgr5-expressing progenitors (Fig. 5H–J). Nine weeks after GLx, Lgr5-derivatives were still present in all taste bud cell types and the surrounding local epithelium (Fig. 5G and data not shown), suggesting that adult Lgr5+ cells surrounding taste buds in posterior papillae are a progenitor population contributing to taste bud regeneration upon injury.
Figure 5
Figure 5
Lgr5 cells can contribute to taste bud regeneration after GLx.
In this report, we demonstrate that Lgr5-expressing cells in the newborn give rise to taste buds in both the anterior and the posterior regions of the tongue. Lgr5+ cells can contribute to all the lineages of the taste bud, including various receptor cell types and local keratinocytes. In the adult, Lgr5 is expressed by the epithelium surrounding adult posterior taste buds and by some intragemmal type IV basal cells. Adult posterior Lgr5+ cells survive damage following glossopharyngeal nerve injury and contribute to regenerating taste buds. Lgr5 is not expressed in anterior taste buds in the adult.
Taken together, our data is most consistent with a model in which extragemmal Lgr5 expression identifies a posterior taste bud stem/progenitor cell population. Data to support this model includes the finding that lineage tracing of Shh-expressing cells, which is confined to the intragemmal region and does not provide long-term labeling of regenerated taste buds. Derivatives of Lgr5+ cells were found in the adjacent extragemmal epithelium in every instance of long-term Lgr5 lineage tracing in which taste buds were labeled. Labeling confined to the intragemmal taste bud was observed only after short chase periods. Hence, long-term repopulating cells are likely to be confined to the extragemmal domain.
Lgr5-expressing cells function as taste bud progenitor cells throughout the tongue during early postnatal life, but Lgr5 expression is lost in adult anterior taste papillae. Therefore Lgr5-expression does not mark a progenitor cell in that location. Thus, further studies are necessary to fully characterize stem/progenitor cells in the full range of taste receptors. We recently demonstrated that Hopx expression identifies multiple adult epithelial stem cell populations with subtle differences from Lgr5+ cells with regard to the ability of expressing cells to proliferate and regenerate under physiological conditions [23], [24]. Hopx is strongly expressed by slowly cycling, BrdU-retaining stem cells in the hair follicle bulge and intestinal crypt. In taste papillae, Hopx is absent from basal epithelium surrounding taste buds, but present elsewhere within basal cells of tongue epithelium (Epstein laboratory, unpublished data). Combinations of markers such as Lgr5, Hopx, Shh and others may provide tools to identify and to more precisely define progenitor cells that contribute to taste bud formation and regeneration during embryogenesis and adulthood.
In summary, our studies identify Lgr5 as a marker of progenitor cells that will contribute to multiple taste bud populations during development. In the adult, Lgr5-expressing taste bud progenitors are restricted to the posterior tongue, where they are capable of regenerating all the cell types of the mature taste bud after injury induced by denervation. Further definition of the signals that mediate activation of taste bud stem cells may be useful therapeutic targets to hasten recovery of taste and appetite in patients suffering from iatrogenic loss of these faculties.
Figure S1
GFP staining of adult wild-type mouse CV papillae. Non-specific signals are detected at apical tips of taste bud cells (asterisks) and surface layers of the tongue in wild type mice. Scale bars = 50 µm.
(TIF)
Figure S2
Sox2 within taste buds mark type I taste receptor cells. Double staining of Sox2 of taste papillae with type II (PLC β2, A) and III (CA4, B)-specific markers. Sox2 expression is detected in both intragemmal and extragemmal epithelial cells, and intragemmal Sox2 is expressed in non type II/III cells. The taste bud is outlined by dotted white line. Scale bars = 20 µm.
(TIF)
Figure S3
Control staining of uninduced Lgr5EGFP-ERCre/+;R26Tom/+ mice. TdTomato/RFP and CK8 staining of the CV (A) and FG papillae (B) from an adult Lgr5EGFP-ERCre/+;R26Tom/+ mouse that has not been injected with tamoxifen, demonstrating no ectopic expression of tdTomato/RFP. Scale bars = 50 µm.
(TIF)
Figure S4
Taste bud regeneration after transection of bilateral glossopharyngeal nerves (GLx). Representative images of hematoxylin/eosin-stained sections of CV papillae at indicated time points after GLx. Taste buds gradually disappear by 14 days after GLx followed by the appearance of normal-looking taste buds (3 w, 4 w, arrowheads). Numerous regenerated taste buds are present 9 weeks after GLx. Scale bars = 50 µm.
(TIF)
Acknowledgments
We thank members of the Epstein laboratory for valuable discussions.
Funding Statement
This work was supported by the National Institutes of Health (NIH) (2T32 HL007843-16) and National Marfan Foundation (RJ) and the NIH (R01 HL071546, U01 HL100405), the Spain fund for Regenerative Medicine, and the W. W. Smith Endowed Chair (JAE). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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