mobilizing transit-amplifying cell-derived ectopic progenitors … · 1 mobilizing transit-....
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Mobilizing transit-amplifying cell-derived ectopic progenitors prevents hair loss from
chemotherapy or radiation therapy
Wen-Yen Huang1, Shih-Fan Lai1,2, Hsien-Yi Chiu1,3,4, Michael Chang5, Maksim V. Plikus6,
Chih-Chieh Chan4, You-Tzung Chen7, Po-Nien Tsao8,9, Tsung-Lin Yang9,10,11, Hsuan-Shu Lee12, 13,
Peter Chi14,15, Sung-Jan Lin1,4,9,11*
1Institute of Biomedical Engineering, College of Medicine and College of Engineering, National
Taiwan University, Taipei, Taiwan.
2Division of Radiation Oncology, Department of Oncology, National Taiwan University Hospital and
College of Medicine, Taipei, Taiwan.
3Department of Dermatology, Hsin-Chu Branch, National Taiwan University Hospital, Hsin-Chu
City, Taiwan.
4Department of Dermatology, National Taiwan University Hospital and College of Medicine, Taipei,
Taiwan.
5Sophie Davis School of Biomedical Education, City University of New York, New York, NY, USA.
6Department of Developmental and Cell Biology, Sue and Bill Gross Stem Cell Research Center and
Center for Complex Biological Systems, University of California, Irvine, Irvine, CA, USA.
7Institute of Medical Genomics and Proteomics, National Taiwan University College of Medicine,
Taipei, Taiwan.
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8Department of Pediatrics, National Taiwan University Hospital and College of Medicine, Taipei,
Taiwan.
9Research Center for Developmental Biology and Regenerative Medicine, National Taiwan
University, Taipei, Taiwan.
10Department of Otolaryngology, National Taiwan University Hospital and College of Medicine,
Taipei, Taiwan.
11Graduate Institute of Clinical Medicine, National Taiwan University College of Medicine, Taipei,
Taiwan.
12Department of Internal Medicine, National Taiwan University Hospital and College of Medicine,
Taipei, Taiwan.
13Institute of Biotechnology, National Taiwan University, Taipei, Taiwan.
14Institute of Biochemical Sciences, College of Life Science, National Taiwan University, Taipei,
Taiwan.
15Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Running title: Hair regenerates from transit amplifying cells
Key words: Alopecia, radiotherapy, chemotherapy, transit amplifying cell, stem cell, anagen hair
follicle repair, Wnt
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Abbreviations: BgSC: bulge stem cell; DP: dermal papilla; HF: hair follicle; HFSC: hair follicle
stem cell; IR: ionizing radiation; IRS: inner root sheath; ORS: outer root sheath; SC: stem cell; SHG:
secondary hair germ; ShgSC: secondary hair germ stem cell; TAC: transit amplifying cell.
Financial support: This work was supported by Taiwan Bio-Development Foundation (TBF) (S.J.
Lin), a Taiwan National Health Research Institutes grant (EX104-10410EI to S.J. Lin), Taiwan
Ministry of Science and Technology grants (105-2627-M-002-010 to S.J. Lin;
105-2314-B-002-073-MY4 to P. Chi; 106-2314-B-002-133-MY3 to S.F. Lai), National Taiwan
University Hospital grants (105-S3010, 104-P04 to S.J. Lin), NIH NIAMS grants (R01-AR067273,
R01-AR069653 to M.V. Plikus) and Pew Charitable Trust (M.V. Plikus).
*Correspondence to:
Sung-Jan Lin, MD, PhD, Institute of Biomedical Engineering, College of Medicine and College of
Engineering, National Taiwan University, #1, Section 1, Jen-Ai Road, Taipei, Taiwan 100. Tel:
+886-2-23562141, Fax: +886-2-23934177. E-mail: [email protected]
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Abstract
Genotoxicity-induced hair loss from chemotherapy and radiotherapy is often encountered in cancer
treatment, and there is a lack of effective treatment. In growing hair follicles (HF), quiescent stem cells
(SC) are maintained in the bulge region and hair bulbs at the base contain rapidly dividing, yet
genotoxicity-sensitive transit-amplifying cells (TAC) that maintain hair growth. How
genotoxicity-induced HF injury is repaired remains unclear. We report here that HF mobilize ectopic
progenitors from distinct TAC compartments for regeneration in adaptation to the severity of
dystrophy induced by ionizing radiation (IR). Specifically, after low-dose IR, keratin5+ basal hair bulb
progenitors, rather than bulge SC, were quickly activated to replenish matrix cells and regenerated all
concentric layers of HF, demonstrating their plasticity. After high-dose IR, when both matrix and hair
bulb cells were depleted, the surviving outer root sheath cells rapidly acquired a SC-like state and
fueled HF regeneration. Their progeny then homed back to SC niche and supported new cycles of HF
growth. We also revealed that IR induced HF dystrophy and hair loss and suppressed WNT signaling
in a p53- and dose-dependent manner. Augmenting WNT signaling attenuated the suppressive effect
of p53 and enhanced ectopic progenitor proliferation after genotoxic injury, thereby preventing both
IR- and cyclophosphamide-induced alopecia. Hence, targeted activation of TAC-derived progenitor
cells, rather than quiescent bulge SC, for anagen HF repair can be a potential approach to prevent hair
loss from chemotherapy and radiotherapy.
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Introduction
Chemotherapy and radiotherapy are widely employed in the treatment of various cancers (1,2).
Both ionizing radiation (IR) and a substantial proportion of chemotherapeutic agents exert their
treatment effects against cancer cells by inducing DNA damage (1-3). Despite extensive efforts made
to minimize off-target injuries, damage to normal tissues is still inevitable (2,4-6). Hair loss is a
common side effect (7-9). It brings psychosocial stress, compromises patients’ sense of personal
identity and even jeopardizes the willingness for treatment (8,10). Prevention of such hair loss is still
an unmet clinical need (7,8).
Hair follicles (HFs) are a dynamic organ that undergo life-long growth cycles, consisting of
anagen (active growth), catagen (regression) and telogen (relative rest) phases (Fig. 1A) (9). Both
telogen and anagen HFs share an upper permanent segment, spanning from the follicular
infundibulum to the bulge (Fig. 1A) (9,11-13). The structures below the bulge are not permanent (Fig.
1A) (9,11-13). In telogen, the lower segment shrinks to a minimum structure of secondary hair germ
(SHG) (9,11,12). In anagen, the lower segment expands dramatically into a long cylinder where
distinct populations of transit amplifying cells (TACs) reside. Among them, outer root sheath (ORS)
cells, located immediately below the bulge, are connected with an enlarged hair bulb where hair
matrix germinative cells surrounding the dermal papilla (DP) actively multiply to generate concentric
cellular layers of distinct differentiations to support hair elongation (9,13-15). Since at any given
time the majority of human scalp HFs are in anagen (9), this highly proliferative nature makes
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anagen HFs one of the most sensitive organs to genotoxic injury (7,16,17).
The slow-cycling long-lived HF stem cells (HFSCs) are constantly preserved in the bulge around
hair cycles (11,12,18). In addition to these quiescent bulge SCs (BgSCs), telogen HFs house another
population of more active SCs in SHG (SHG stem cells (ShgSCs)) (11,12,19,20). During transition
from telogen to anagen, ShgSCs proliferate first to support the formation of the initial hair bulbs
(11,12,19). This is followed by the activation of quiescent BgSCs a few days later, which contribute
to the upper ORS (11,12,19). In contrast, the highly expanded lower segment of anagen HFs lacks
long-lived SCs (9,18).
With the presence of TACs only in the lower segment, how are anagen HFs repaired to resume
the ongoing anagen hair growth following genotoxic injuries? Since quiescent BgSCs are relatively
resistant to genotoxic insults (21), such repair might be driven by BgSCs. However, it would require
complete HF involution and lengthy resetting of the hair cycle. This possibility is contrasted by the
fact that DNA-damaged anagen HFs often bypass telogen involution and resume hair production
without cycle resetting (8,17). Such observations suggest that, in contrast to the telogen-to-anagen
regeneration that relies on the activation of BgSCs and ShgSCs, anagen HFs can mobilize mother
progenitor cells for repair.
In this work, we attempt to explore the mechanisms and map the progenitor sources underlying
the regenerative responses of anagen HF repair following ionizing radiation (IR) injury. We provide
evidence that HFs are able to employ ectopic progenitor cells from distinct TAC compartments for
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repair in adaptation to the severity of genotoxic damage. We also demonstrate that efficient
mobilization of TAC-derived ectopic progenitor cells for anagen HF repair can be a strategy to
prevent hair loss from chemotherapy and radiotherapy.
Materials and Methods
Mice
All animal experiments were approved by the Institutional Animal Care and Use Committee
(IACUC) of National Taiwan University. K5CreER mice were provided by Chen CM (22),
Lgr5EGFP-Ires-CreERT2 mice were from Clevers H (23), and K19
CreER mice were from Gu G (24). p53
null mice, Ctnnb1flox/flox mice (25) and R26LSL
tdTomato mice were from Jackson lab. C57BL/6 mice
were from Taiwan National Laboratory Animal Center. For IR and invasive experiments, animals
were anesthetized by Tiletamine-Zolazepam (Telazol®).
Radiation exposure
The dorsal hair of female mice at postnatal day 30 was carefully shaved by an electric shaver.
Around two days later when dorsal HFs were in early full anagen (~postnatal day 32), single doses
(2Gy or 5.5Gy) of gamma irradiation were given from the dorsal side by a 137Cs source (dose rate
3.37Gy/min, gamma irradiator IBL 637 from CIS Bio International, France). For comparison,
littermate control with the same genetic background was used. Mice were consistently irradiated in
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the afternoon.
Lineage tracing experiment
To label basal cells and BgSCs, K5CreER/+
; R26LSLtdTomato/+ and K19
CreER/+; R26LSL
tdTomato/+ mice
received a single intraperitoneal injection of tamoxifen (TAM; Sigma) (0.1mg/g of body weight)
24hrs prior to irradiation. To label cells in the lower segment of epithelial strand at 5.5 Gy of IR,
Lgr5EGFP-Ires-CreERT2/+
; R26LSLtdTomato/+ mice received a single dose of tamoxifen (0.05mg/g of body
weight) at 48hrs after radiation.
Inhibition of Wnt/β-catenin signaling
Inhibition of Wnt/β-catenin signaling in the epithelium was achieved by the conditional deletion
of Ctnnb1 in K5CreER/CreER
; Ctnnb1flox/flox mice by tamoxifen (0.1mg/g body weight) at 6 and 12hrs
after irradiation or by using specific inhibitors IWR1 and IWP2 (Sigma). Both IWR1 and IWP2 were
reconstituted in DMSO, and DMSO was used as a control. Mice were subcutaneously injected with
IWR1 and IWP2 at 48, 72 and 96hrs post irradiation, totaling 12.5μg/g body weight for each dose.
Skin was harvested at day 5 for examination.
Histology, immunostaining and TUNEL staining
Skin specimens were fixed at 4℃ overnight either in formalin-acetic-alcohol solution for
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paraffin embedment or 4% paraformaldehyde for OCT (Sakura Finetek) embedment. Specimens
were sectioned and stained with hematoxylin and eosin (H&E). Apoptotic cells were detected by
DeadEndTM Fluorometric TUNEL System (Promega). Cryosections were used to visualize tdTomato
fluorescence of lineage tracing. Immunohistochemistry and immunofluorescence staining were
performed with routine antigen retrieval as suggested by the antibody manufacturers. Super
SensitiveTM IHC Detection Systems (BioGenex) were used for the detection of horseradish
peroxidase activity. The antibodies used were described in Supplementary Table S1.
Image acquisition and quantification
All fluorescent images were acquired on the confocal microscope (SP5, Leica). To quantify
BrdU+ and TUNEL+ cells, we acquired 1024x1024 pixels sequential scans with a 63x oil immersion
objective lens (1.4 NA). Hair matrix was counted as epithelial cells below the top of DP. Germinative
cells are epithelial cells adjacent to DP, and basal hair bulb cells are basal cells located on the outer
surface of the hair bulb abutting dermal sheaths.
Quantification of γ-H2AX foci
DNA double-strand breaks were determined by γ-H2AX foci as previously described (26).
Briefly, the 3-dimensional fluorescent images were reconstituted by approximately 10-15 images of
serial 2-dimensional Z-stacks of confocal images. Data were analyzed using the software
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MetaMorph 7.7. Foci within Hoechst-stained nucleus were scored by the value of pixels after the
focus threshold was set manually. 5 pixels were considered as a standard for single DNA
double-strand breaks based on the few discrete γ-H2AX foci generated in the nucleus of unirradiated
control specimen. Because extensive γ-H2AX foci appeared after irradiation, individual foci could
not be distinguished accurately. We compared the total value of positive pixels within the nucleus in
selected cells with the standard 5 pixels/focus to estimate the number of foci in an entire nuclear
region.
RNA-sequencing analysis
Keratinocytes of irradiated skin were collected at different time points after irradiation. Total
RNA from keratinocytes was extracted using TRI reagent® solution (Thermo) for the following
RNA-seq library preparation and sequencing. All procedures were carried out according to the
protocol from Illumina. The libraries were sequenced on the Illumina NextSeq 500 platform using 75
single-end base pair strategy, and 10 million reads per sample were generated. Gene Ontology (GO)
and KEGG analysis were performed using DAVID (https://david.ncifcrf.gov/) (27).
Quantitative RT-PCR
Total RNA from keratinocytes of irradiated skin collected at different time points was extracted
using TRI reagent® solution (Thermo). The RNA was reverse transcribed into cDNA using
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RevertAid H Minus First Strand cDNA Synthesis Kit (Thermo). In bead implantation experiment,
HF epithelial cells were isolated from the HFs surrounding Wnt3a and BSA-soaked beads, and the
RNA was extracted and cDNA was amplified by using REPLI-g WTA single cell kit (QIAGEN).
Quantitative PCR analysis was performed using SYBR Green qPCR Master Mix (Thermo) on an
ABI 7900HT Real-Time PCR System (Applied Biosystems). Sequences of gene-specific primers
used were described in Supplementary Table S2.
FACS
The dorsal skin of seven-week-old female mice were used for the sorting of inactive ShgSCs.
For the sorting of activated ShgSCs, dorsal hairs of seven-week-old female mice were plucked to
activate ShgSCs 2 days before skin specimen collection (28). The dorsal skin of 32-day-old mice
were irradiated with 5.5Gy of IR and skin specimen was collected at 72hr. Cell preparation for FACS
was performed as described (29). The following antibodies were used: CD34-FITC (eBioscience,
11-0341, 1:50), Sca1-PE-Cy7 (eBioscience, 25-5981, 1:50) and p-cadherin-PE (R&D systems,
FAB761P, 1:100). FACSAria III sorter equipped with Diva software (BD, Bioscience, San Jose, CA)
was used for sorting. Total RNA from sorted cells was extracted using MessageBOOSTERTM cDNA
Synthesis from Cell Lysates Kit (Epicentre).
Protein administration experiment
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Intracutaneous implantation of protein-coated beads was performed as described (30). Human
Wnt3a recombinant protein (R&D systems) was re-suspended in 1mg/ml BSA solution at 1mg/ml.
Affinity affi-gel blue gel beads (Bio-Rad) were then suspended in 5μl protein solution, either control
(1mg/ml BSA) or experimental (1mg/ml Wnt3a), at 4℃ for 2hrs. Approximately 100 beads were
implanted into skin immediately after irradiation. Mice were sacrificed at different time points
post-irradiation. To visualize HFs, skin specimens were dehydrated in ethanol with graded
concentrations and then immersed in xylene until it became transparent. The skin specimens were
then further processed for histological examination and immunofluorescent staining.
Statistical analysis
Statistical comparison was performed using the software Prism (GraphPad). An unpaired
Student’s t-test was used to compare data sets with two groups. To compare three or more groups, we
performed One-Way ANOVA followed by Bonferroni’s multiple comparison. Data were presented as
mean ± standard error. P-values were considered significant when less than 0.05.
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Results
Dose-dependent HF dystrophy after IR and two tempospatially distinct regenerative attempts
To characterize the effect of IR, mice were irradiated with 2Gy and 5.5Gy on postnatal day 32
when dorsal HFs were in early full anagen (Fig. 1A). In five to ten days, there was a dose-dependent
hair loss and HF dystrophy (Fig. 1B and C; Supplementary Fig. S1A). At 2Gy, the initial reduction of
matrix cells and HF shortening were recovered by days 3 and 4 (Fig. 1C-E). At 5.5Gy, HFs
progressively shrank to slender epithelial strands by day 3, followed by restoration of anagen
morphology and length between days 5 and 7 (Fig. 1C and D). Around day 10, HFs of the
unirradiated, 2Gy and 5.5Gy groups entered catagen, indicated by decreased cell proliferation and
increased apoptosis (Fig. 1C, F-I). Afterwards, HFs could resume a new anagen in 2Gy and 5.5Gy
groups (Supplementary Fig. S1A), indicating the hair loss was transient.
We then analyzed cell death and proliferation. TUNEL staining and cleaved caspase-3 staining
were performed to detect apoptosis and both assays exhibited a similar trend (Fig. 1F, G, J).
Apoptosis was more extensive and persistent after 5.5Gy than 2Gy (Fig. 1F, G, J). After 2Gy
exposure, cell proliferation almost entirely halted after 6hrs and then increased at 12 and 48hrs (Fig.
1H and I). This early proliferative response successfully restored hair bulb structures and HF length
between 72 and 96hrs (Fig. 1C and D). After 5.5Gy exposure, a similar regenerative response, albeit
with lower proliferation, was observed between 12 and 48hrs (Fig. 1H and I). However, proliferation
almost entirely ceased again at 72hrs. Progressive HF shrinkage between 0 to 72hrs indicated failure
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of the early regenerative attempt to compensate for the more severe cell death (Fig. 1C, F, G, J).
Importantly, a second late proliferative attempt was observed in the lower tip of HFs at 96hrs (Fig.
1H and I) and led to HF elongation and restoration of hair bulbs (Fig. 1C- E).
Next, we examined whether these regenerative attempts led to production of mature hair shafts.
At 2Gy, differentiation toward inner root sheath (IRS) and hair cortex was only transiently disrupted
between 36 and 48hrs (Supplementary Fig. S1B). At 5.5Gy, a lengthier and more severe disruption
was induced, yet differentiation was eventually restored (Supplementary Fig. S1C).
These results show that, depending on the severity of IR damage, HFs activate two distinct
regenerative responses: early regenerative attempt between 12 and 48hrs and late regenerative
attempt after 72hrs.
K5+ basal hair bulb keratinocytes preferentially proliferate during the early regenerative
attempt
Next, we tried to identify cells contributing to early regenerative attempts. In normal hair bulbs,
keratin 5 (K5) is exclusively expressed in basal cells (Fig. 2A, 0hr). However, 12 to 36hrs after 2Gy
exposure, K5+ cells extended into the suprabasal positions (Fig. 2A and B). TUNEL showed that,
after 2Gy, apoptosis was more prominent in suprabasal K5negative matrix and germinative cells than
K5+ cells (Fig. 2A, C, and D; Supplementary Fig. S2A), and that apoptosis of K5+ cells only slightly
increased (Fig. 2C). BrdU pulse labeling showed these K5+ cells were proliferative (Fig. 2E, yellow
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arrowheads, and F). During the same period, proliferation of K5negative suprabasal matrix cells nearly
ceased at 6hrs and was progressively restored only by 48hrs (Fig. 2E and G). Analysis of
double-stranded DNA breaks by γ-H2AX expression also showed faster repair of DNA damage in
K5+ basal hair bulb cells (Supplementary Fig. S2B and B’). Together, basal K5+ cells are more
resistant to IR than suprabasal K5negative matrix and germinative cells, and become proliferative to
support early regenerative attempts.
5.5Gy exposure induced a similar increase in suprabasal K5+ cells (Fig. 2A and B), yet their
proliferation was delayed compared to the 2Gy group (Fig. 2E and F). Notably, higher apoptosis in
both K5+ and K5negative cells was detected after 5.5Gy during the early regenerative attempt (Fig. 2A,
white arrowheads, C and D). K5+ cells also showed more persistent expression of DNA damage
markers (Fig. 2H; Supplementary Fig. S2C and C’). These data suggest that K5+ cells and their
progeny sustain catastrophic IR injury. Without sufficient resupply from the K5+ compartment,
K5negative matrix cells, which also proliferate poorly (Fig. 2E and G), undergo eventual collapse,
leading to failure of the early regenerative attempt.
K5+ basal hair bulb cells replenish germinative population and contribute to all layers of
recovered HFs
To further confirm the cellular source for early regenerative attempts (Fig.3A), we lineage
traced K5+ cells in K5CreER
; R26LSLtdTomato mice (Fig. 3B). Injection with tamoxifen 24hrs prior to IR
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allowed successful and exclusive labeling of basal, but not germinative cells in the hair bulb (Fig. 3B,
0hr). After 2Gy exposure, labeled cells expanded into suprabasal positions at 12hr (Fig. 3B, yellow
arrowhead), replenished the germinative compartment (Fig. 3B, white arrowheads) and contributed
to all layers of repaired hair bulbs, including hair shafts (Fig. 3B, white arrow), between 24 and
36hrs. In control HFs, most of the labeled cells remained in the basal position even after 36hrs (Fig.
3B). Quantitatively, progeny of K5+ lineage progressively increased, accounting for about 60% of all
matrix cells at 36hrs (Fig. 3C). The data underscore that, following IR, K5+ basal hair bulb cells
display high lineage plasticity.
Next, we determined the contribution of BgSCs. Neither apoptosis (Fig. 3D) nor proliferation
(Fig. 3E) was detected in the bulge. Lineage tracing in K19CreER
; R26LSLtdTomato mice did not show
BgSC expansion (Fig. 3F). The results indicate that BgSCs survive 2Gy IR injury but do not actively
contribute to early regenerative attempts.
K5+ ORS cells are remodeled into the epithelial strand during the late regenerative attempt
The results above show that the remaining short epithelial strand at 72hrs serves as a platform
for the late regenerative attempt. To determine the origin of the epithelial strand, we performed
lineage tracing in K5CreER
; R26LSLtdTomato mice (Fig. 4A) following tamoxifen administration 24hrs
prior to IR. This protocol labeled basal cells in the ORS in addition to basal cells of the bulb (Fig.
4A). As HFs regressed between 24 and 72hrs, a larger portion of the epithelial strand became
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composed of the K5+ progeny (Fig. 4A). Since K5+ basal hair bulb cells fail to survive 5.5Gy injury,
we conclude that the epithelial strand originates from the K5+ ORS cells that are more radioresistant,
and that basal ORS progeny fuel successful HF regeneration during late regenerative attempts (Fig.
4A).
Lower tip cells acquire a stem cell-like property and undergo stepwise activation with BgSCs
for the late regenerative attempt
After 5.5Gy, cell proliferation was largely halted at 72hrs (Figs. 1H and I, 4B). By 84hrs,
proliferation was first resumed in p-cadherin+ lower tip cells (Fig. 4B, white arrowheads). At 96hrs,
more lower tip cells proliferated as they continued to regenerate new hair bulbs (Fig. 4B). We did not
detect apoptosis of BgSCs (Fig. 4C). Continuous BrdU labeling showed that BgSCs did not start
proliferating until day 5 post-IR (Fig. 4D, white arrowheads), when the new hair bulb already
regenerated (Fig. 1C). Lineage tracing of BgSCs in K19CreER
; R26LSLtdTomato mice showed that
BgSCs contributed to the suprabulbar ORS cells right below the bulge, but not to the regenerated
hair bulbs (Fig. 4E). These results indicate that the lower tip cells fuel the initial late regenerative
attempt. This parallels the stepwise activation of epithelial progenitor populations during
physiological telogen-to-anagen transition, when ShgSCs, rather than quiescent BgSCs, fuel early
HF growth (12,19).
We considered that cells in the lower segment of the epithelial strand acquire SC-like
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characteristics. We compared the epithelial strand structure of 5.5Gy-irradiated anagen HFs with
normal telogen HFs. Typical BgSC markers, CD34 and K15 (31,32) , were still maintained in the
bulge (Supplementary Fig. 3A). However, cells at the lower end of the epithelial strand were
CD34/K15 double-negative, yet positive for p-cadherin, Sox9 and Lgr5 promoter activity, markers of
the normal telogen ShgSCs (Fig. 4F and G; Supplementary Fig. 3A) (12,20,33). Lack of AE13, AE15
and K75 keratin expression shows that lower epithelial strand cells do not prematurely differentiate
toward inner anagen HF structures (Supplementary Fig. 3A). We then FACS-isolated these lower tip
cells using a Sca1low CD34low p-cadherinhigh marker profile (Supplementary Fig. 3B) (12), and
examined the expression of known ShgSC genes (12). We found Ccnb1, Clca1, Sox4 and Sox6 were
also upregulated in the sorted lower tip cells at 72hrs (Fig. 4H). Taken together, these results show
that following 5.5Gy IR injury, ORS cells were remodeled into the epithelial strand whose lower tip
cells acquired a ShgSC-like progenitor property.
To strengthen the evidence for the cellular dynamics noted above (Fig. 4I), we performed
additional lineage tracing using Lgr5EGFP-Ires-CreERT2 mice, which allowed for specific tracing of the
lower tip cells (Fig. 4J; Supplementary Fig. S4). Consistent with the prior report (34), in unirradiated
Lgr5EGFP-Ires-CreERT2 mice, ORS cells and suprabasal hair bulb cells were labeled after tamoxifen
induction (left panel, Fig. 4J). In the 5.5Gy group, although the epithelial strand was negative for
Lgr5 by immunostaining (Supplementary Fig. S3A), its lower portion was distinctly positive for the
Lgr5 promoter activity (Fig. 4G). Twenty four hours after tamoxifen injection to Lgr5EGFP-Ires-CreERT2
;
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R26LSLtdTomato mice at 48hrs after 5.5Gy, labeled cells were exclusively found in the lower portion of
the epithelial strands of all HFs examined (n=50; right panel, Fig. 4J), with higher incidence in the
lower tip. These labeled Lgr5 progeny contributed to the ORS, the entire hair bulb and hair shafts of
the repaired HFs (right panel, Fig. 4J; Supplementary Fig. S4).
Further tracing showed that the progeny of labeled Lgr5 cells homed back to the SHG and bulge
when repaired HFs eventually transitioned to telogen (d17, right panel, Fig. 4J), and that in the next
cycle they formed the new lower segment of the anagen HF (d35, right panel, Fig. 4J). These results
reveal expanded plasticity of ORS cells following IR and underscore IR-induced acquisition of SC
properties.
Genotoxic injury disrupts WNT signaling that is required for late regenerative attempt
Because HF regeneration from ORS-derived progenitors represents a novel repair mechanism,
we aimed to clarify its molecular basis. First, we compared epithelial cell transcriptomes at different
time points before and after 5.5Gy of IR by RNA-sequencing. Gene ontology (GO) enrichment
analysis revealed several biological processes altered following IR (Fig. 5A). We screened for
signaling pathways downregulated between 0 and 24hrs and upregulated between 24 and 72hrs. We
found that WNT and hedgehog pathways fit this trend (Supplementary Table S3). Hedgehog
signaling has been shown to be downregulated by cyclophosphamide in growing HFs (35).
WNT signaling is activated in ShgSCs at the onset of physiological anagen and is crucial for
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20
normal hair cycle progression (36-38). The transcript and protein levels of Lef1, a downstream
mediator of WNT signaling in HFs, were prominently suppressed after IR and restored only by 96hrs
post-IR (Fig. 5B and C). This was accompanied by an increase in nuclear β-catenin in the lower tip
cells 72-96hrs post-IR (Fig. 5D). WNT ligands are secreted by HF epithelium and help to maintain
proper epithelial-mesenchymal interaction during anagen (36,39-41). We found that Wnt3a levels
were diminished between 24 and 48hrs post-IR, but later rebounded from 72hrs onward at the base
of the epithelial strand (Fig. 5E and F). These results show that 5.5Gy disrupts WNT signaling and
that its reactivation correlates with late regenerative attempts. In comparison, after 2Gy exposure,
levels of Wnt3a and Lef1 were suppressed only transiently and partially (Supplementary Fig.
S5A-D). Therefore, higher IR doses induce more severe suppression of WNT signaling.
To determine whether WNT signaling reactivation is required for late regenerative attempts, we
pharmacologically disrupted WNT ligand secretion with IWR1 and IWP2 inhibitors and found that
the late regenerative attempt was attenuated (Fig. 5G). We also disrupted β-catenin in K5CreER
;
Ctnnb1flox/flox mice after 5.5Gy of IR and found that the late regenerative attempt was abolished (Fig.
5H). Therefore, reactivation of WNT signaling is essential for the late regenerative attempt. This
parallels the requirement for WNT signaling during normal HFSC activation upon telogen-to-anagen
transition (36,38)
p53 is required for IR-induced HF dystrophy and suppression of WNT signaling
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p53 has been shown to mediate pathological changes of chemotherapy-induced hair loss and
IR-induced injury to other organs (42,43). Its role in IR-induced HF dystrophy remains unclear. We
found that p53 was induced by IR in hair bulbs, but not DP, and that p53 expression was more
extensive and persistent at 5.5Gy than 2Gy (Fig. 6A). Furthermore, matrix apoptosis, suppression of
proliferation, HF shrinkage and hair loss were not induced in p53 null mice by IR (Fig. 6B-E;
Supplementary Fig. S6A-C). In wild-type mice, IR increased expression of downstream target genes
of p53, Noxa, Bax, and p21, whereas Puma expression was slightly decreased from 6 to 48hr and
transiently elevated at 72hr (Fig. 6F). In p53 null mice, the baseline expression of Bax and p21 was
higher than wild-type mice while Noxa and Puma were lower than wild-type mice (Fig. 6F). After IR,
compared to wild-type mice, decreased expression of Bax, Noxa and Puma was observed in p53 null
mice and p21 was only slightly increased at 24hr. This might help to explain the decreased apoptosis
and unsuppressed cell proliferation after IR in p53 null mice.
Comparison of 2Gy and 5.5Gy-induced injuries revealed a correlation between the duration of
p53 activation and more severe and persistent WNT signaling suppression, suggesting that p53 might
be involved in mediating IR-induced WNT suppression. We found that the basal mRNA expression
of Wnt3a and Lef1 at 0hr was significantly higher in p53 null mice than in p53 wild-type mice (Fig.
6G). The higher WNT signaling activity in p53 null mice is consistent with the prior report showing
the inhibition of WNT signaling by p53 (44). In p53 wild-type mice, both Wnt3a and Lef1 expression
were prominently suppressed by 5.5Gy of IR and were restored again at 72hrs and 96hrs,
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respectively. In p53 null mice, although the Wnt3a expression was decreased after IR, it was still
higher than that in p53 wild-type mice at 6, 24 and 96hrs. Lef1 expression was not downregulated
until 24hrs but its levels in p53 null mice were much higher than that of p53 wild-type at all time
points. Consistent with this, we found that protein expression of Wnt3a and Lef1 was not suppressed
by IR in p53 null mice (Fig. 6H and I). Judging from Lef1 expression, WNT signaling was
maintained at a higher level in p53 null mice and this might contribute in part to the attenuated HF
dystrophy after IR.
Local delivery of WNT ligands prevents IR and cyclophosphamide-induced alopecia by
enhancing ectopic progenitor cell proliferation
Since WNT ligands produced by anagen HF epithelium are known to maintain anagen
progression (36,38,39) and since WNT signaling undergoes early suppression after IR, we posited
that maintaining WNT signaling might promote HF regeneration, in part by bypassing the
suppressive effect of p53 on cell proliferation. To test this, we delivered Wnt3a-soaked beads into the
5.5Gy irradiated skin (Fig. 7A). We found that hairs continued to emerge in the Wnt3a-treated skin
(Fig. 7A; Supplementary Fig. S6D) with reduced HF dystrophy and faster restoration of anagen
structures (Fig. 7B; Supplementary Fig. S6E and F). Wnt3a treatment preserved Lef1 expression
(Supplementary Fig. S7A), but did not prevent p53 activation and apoptosis (Fig. 7C and D;
Supplementary Fig. S7B). The latter was only slightly decreased at 24hrs post-IR (Fig. 7C and D).
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Analysis of gene expression of HF epithelial cells from Wnt3a-treated and control (BSA)-treated
skin showed that Wnt3a treatment significantly inhibited the upregulation of Bax, Noxa, and p21, but
increased the expression of Puma after IR (Fig.7 E). The upregulation of proapoptotic Puma with
downregulation of proapoptotic Bax and Noxa might help to explain that Wnt3a did not largely
suppress IR-induced apoptosis (Fig. 7D). The suppression of p21 expression, an important p53 target
that induces cell cycle arrest, by Wnt3a treatment (Fig.7E) might promote regenerative proliferation.
Indeed, compared to control, an early increase of basal K5+ cell proliferation was observed at 24hrs
and cell proliferation within the hair matrix was maintained at a higher level for at least 72hrs (Fig.
7F, white arrows, and G; Supplementary Fig. S7C). Importantly, the number of matrix cells was
increased in the Wnt3a-treated HF (Supplementary Fig. S7D).
We also tested whether this approach can prevent chemotherapy-induced alopecia.
Cyclophosphamide (CYP) administered on postnatal day 32 also induced extensive hair loss on day
5 (Fig. 7H). Similarly, local delivery of Wnt3a-soaked beads reduced hair loss after CYP treatment
(Fig. 7I). These results demonstrate that maintaining WNT signaling can prevent hair loss from
genotoxic injury by enhancing the regenerative cell proliferation of K5+ basal hair bulb progenitors.
Discussion
Our results show that, rather than deploying long-lived bulge SCs, IR-damaged anagen HFs
mobilize extra-bulge TAC-derived progenitor cells for repair without having to reset their hair cycle
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(Fig. 7J). This ability of HFs to mobilize distinct extra-bulge progenitors for anagen HF repair also
suggests a new therapeutic strategy for hair loss that relies on TACs.
In hair bulbs, germinative and basal bulb cells are thought to represent two distinct lineages
within the TAC population (14). Proliferative germinative cells fuel hair shaft elongation (14,45)
while basal hair bulb cells (also referred to as lower proximal cup cells) are speculated to maintain
the shape of hair bulbs and not to contribute to the inner HF structures (14). We show that K5+ basal
cells serve as SCs for rapid repair of the HF bulb, and that their concealed plasticity is quickly
unveiled upon injury. Previously, colony-forming epithelial SCs were shown to be present in the hair
bulbs (46). It is likely that K5+ basal hair bulb cells can be a source of colony-forming cells. The
employment of local multipotent progenitors within the TACs shortens the time needed for
regeneration and this strategy is advantageous over regeneration via BgSCs. The employment of
BgSCs would require intricate signaling relays and create a significant time delay during their
downward migration toward injured hair bulbs.
We also revealed a novel role for ORS cells of the TAC pool for regeneration. HFs suffering
from a more dystrophic change regenerate from the surviving ORS cells. Although our lineage
studies are not able to directly differentiate between K5+ basal bulb cells and K5+ basal ORS cells,
the two cell populations are known to be distinct in origin and function during anagen (14). K5+ hair
bulb cells broadly apoptose after 5.5Gy, indicating that radioresistant K5+ ORS cells are the most
likely origin for the epithelial strand. Although targeted depletion of SCs can allow differentiated
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cells to gain SC-like properties upon migration into the physiological SC niche (47,48), it remains
unknown if acquisition of SC-like properties can occur ectopically outside the physiological SC
niche. Here we showed that ORS cells can directly acquire a SC-like state ectopically after IR. Since
DP cells are able to convert interfollicular keratinocytes into follicular cells for HF neogenesis upon
close contact (49), the close proximity of lower tip cells to DP suggested that DP cells might play an
important role here by either directly reprogramming ORS cells into a SC-like state or providing
signals for the dedifferentiation of ORS cells through short-range interaction.
The lower tip cells in the epithelial strand not only express markers characteristic of ShgSCs,
but also behave like them. Similar to the telogen-to-anagen transition (12), the late regenerative
attempt displays the step-wise activation of progenitor cells: lower tip cells are activated first to
regenerate hair bulbs, followed by the activation of BgSCs to resupply upper ORS. Their
contribution to the entire hair bulb and all bulb-derived differentiated structures confirms their
multipotency. Furthermore, their progeny home back to the SC niche at the end of the repaired hair
cycle and contribute to the new hair bulb and ORS during the following physiological hair growth
cycle.
The activation of p53, a central mediator of pathological changes following IR injuries in other
organs (43,50), is required for chemotherapy-induced HF dystrophy (42). We revealed its key role in
the response of HFs to IR and also uncovered a complicated crosstalk between IR, p53 and WNT
signaling. We found that IR induces p53 expression in the hair bulb in a dose-dependent manner. In
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26
p53 null mice, neither apoptosis nor dystrophy was induced, indicating the essential role of p53 in
IR-induced hair loss. Since WNT signaling is not inhibited by IR in p53 null mice, our results
suggest that p53 may have dual roles in both inducing apoptosis and suppressing
regeneration-promoting WNT signaling following IR injury. We demonstrated that augmenting
WNT signaling could attenuate the suppressive effect of p53 on cell proliferation, likely through
inhibition of p53-responsive upregulation of p21, to enhance the regenerative program of ectopic
progenitors from TACs following the injury of IR and cyclophosphamide. Because the effect of
applied Wnt3a protein is transient and localized, it potentially represents a new, low-risk clinical
strategy to reduce hair loss after genotoxic injury.
Acknowledgements
We thank the staff of the imaging core and the Flow Cytometric Analyzing and Sorting Core at
the First Core Lab, National Taiwan University College of Medicine, and the staff of the 8th Core
Lab, Department of Medical Research, National Taiwan University Hospital for technical support.
The authors also thank the members of the S.J. Lin lab for their discussion and Drs. Hironobu
Fujiwara, George Cotsarelis and Ralf Paus for their discussion.
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27
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Figure Legends
Figure 1.
Dystrophic changes and regenerative activities in HFs after IR exposure. A, Mouse hair cycle and
introduction of IR injury. Bg: bulge; Mx: matrix; PD: postnatal day; PW: postnatal week; SG:
sebaceous gland. B, IR-induced hair loss. (n=10 in each dose). C-E, Histology and quantification of
HF lengths and matrix cell numbers. F and G, Apoptosis detected by TUNEL staining and
quantification of apoptotic matrix cells. H and I, Cell proliferation mapped by BrdU and
quantification of BrdU+ matrix cells. J, Apoptosis detected by cleaved caspase-3. Statistical
significance was determined by one-way ANOVA followed by Bonferroni’s multiple comparison test.
Blue star * p<0.05, 2Gy vs 0Gy; green star * p<0.05, 5.5Gy vs 0Gy; # p<0.05, 2Gy vs 5.5Gy. Error
bars represent mean ± S.E.M. Dashed line: DP. Scale bar=75μm in (C), 25μm in (F) (H)(J).
Figure 2.
Apoptosis, proliferation, and DNA damage of hair bulb cells during the early regenerative attempt.
Mice were pulse labeled with BrdU 1hr before sampling. A, Double staining with K5 and TUNEL.
B-D, Quantification of K5 and TUNEL expression in (A). B, Proportion of K5+ cells in the matrix. C,
Proportion of K5+ TUNEL+ matrix cells. More severe apoptosis of K5+ cells was observed in 5.5Gy
than 2Gy. D, Proportion of K5negative TUNEL+ matrix cells. E, Double staining with K5 and BrdU. F
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35
and G, Quantification of K5 and BrdU expression in (E). F, Proportion of K5+ BrdU+ matrix cells. G,
Proportion of K5negative BrdU+ matrix cells. Compared to 2Gy, 5.5Gy of IR induced more prolonged
reduction of proliferation in K5negative matrix cells. H, Quantification of γ-H2AX foci in basal hair
bulb cells. Statistical significance was determined by one-way ANOVA followed by Bonferroni’s
multiple comparison test. Blue star * p<0.05, 2Gy vs 0Gy; green star * p<0.05, 5.5Gy vs 0Gy; #
p<0.05, 2Gy vs. 5.5Gy. Error bars represent mean ± S.E.M. Dashed line: DP. Scale bar=25μm.
Figure 3.
Cell origin for the early regenerative attempt after 2Gy of IR. A, Possible cell origin. B and C,
Lineage tracing in K5CreER
; R26LSLtdTomato mice and quantification of labeled cells in the hair matrix.
B, After 2Gy, labeled cells expanded suprabasally (yellow arrowhead), replenished germinative cells
(white arrowheads) and formed hew hair shafts (white arrow). Tam: tamoxifen. C, Proportion of
tdTomato+ matrix cells. Statistical significance was determined by Student’s t test. * p<0.05. Error
bars represent mean ± S.E.M. D, Analysis of BgSC apoptosis by TUNEL. E, Continuous BrdU
labeling for analysis of BgSC proliferation. F, Lineage tracing in K19CreER
; R26LSLtdTomato mice.
Dashed line: DP; Bg: bulge. Scale bar=25μm.
Figure 4.
Remodeling of ORS cells for the late regenerative attempt after 5.5Gy of IR. A, Lineage tracing in
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36
K5CreER
; R26LSLtdTomato mice. B, Cell proliferation mapped by pulse BrdU labeling. The p-cadherin+
lower tip cells started to proliferate at 84hrs (white arrowheads) and regenerated new hair bulb at
96hrs. C, Analysis of BgSC apoptosis by TUNEL. D, Continuous BrdU labeling showed that BgSCs
did not proliferate until day 5 (white arrowheads). E, Lineage tracing of BgSCs in K19CreER
;
R26LSLtdTomato mice. Labeled BgSC progeny did not move out of the bulge until day 5. F,
Immunofluorescence of p-cadherin and Sox9. Similar to SHG (yellow arrowheads), p-cadherin+
lower tip cells were also positive for Sox9 (white arrowheads). G, Lgr5 promoter-driven EGFP
expression in Lgr5EGFP-Ires-CreERT2 mice. The lower tip cells were positive for EGFP. H, Expression of
ShgSC specific genes. Similar to activated ShgSCs, several specific genes were upregulated in lower
tip cells at 72hrs. I, Possible cell origin for late regenerative attempts. J, Lineage tracing in
Lgr5EGFP-Ires-CreERT2
; R26LSLtdTomato mice. Error bars represent mean ± S.E.M. Scale bar=25μm.
Figure 5.
WNT signaling is suppressed by IR and its reactivation is required for late regenerative attempts. A,
Cellular processes affected by 5.5Gy based on the comparative GO-enrichment analysis of the
transcriptomes of the epithelial cells. B and C, Quantitative RT-PCR and immunofluorescence for
Lef1 expression after 5.5Gy of IR. D, Immunofluorescence of β-catenin. Nuclear localization of
β-catenin was detected in the lower tips between 72 and 96hrs. E and F, Quantitative RT-PCR and
immunofluorescence for Wnt3a after 5.5Gy of IR. G, Inhibitor for WNT secretion and WNT
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37
signaling by IWP2 and IWR1, respectively. H, Inhibition of epithelial WNT/β-catenin signaling by
ablating Ctnnb1 in keratinocytes of K5CreER
; Ctnnb1f/f mice. * p<0.05, compared to 0hr, by Student’s
t test. Error bars represent mean ± S.E.M. Scale bar=25μm in (C) (D) (F), 75μm in (G) (H).
Figure 6.
WNT ligand production and WNT signaling are not inhibited in p53 null mice after 5.5Gy of IR. A,
Immunohistochemistry for p53. B, Apoptosis detected by TUNEL staining. C, Cell proliferation
mapped by BrdU pulse labeling. D, IR-induced hair loss was not observed in p53 null mice 5 days
after IR. E, Histology showed no dystrophic changes in HFs of p53 null mice after IR. F,
Quantitative RT-PCR for Bax, Noxa, Puma, and p21 expression in epithelial cells of p53 WT and p53
null mice after 5.5Gy of IR, respectively. G, Quantitative RT-PCR for Wnt3a and Lef1 expression in
epithelial cells of p53 WT and p53 null mice after 5.5Gy of IR. H, Immunofluorescence for Wnt3a. I,
Immunofluorescence for Lef1. Dashed line: DP. Scale bar=75μm. Blue star * p<0.05, compared to
0hr of p53 WT; green star * p<0.05, compared to 0hr of p53 null; # p<0.05, p53 WT vs p53 null.
Error bars represent mean ± S.E.M. WT: wild type.
Figure 7.
Enhancement of WNT signaling prevents IR and cyclophosphamide-induced alopecia by boosting
the early regenerative attempt. A, Subcutaneous injection of Wnt3a-soaked beads (blue beads)
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38
maintained hair growth after 5.5Gy of IR. Dashed circles indicate bead-implanted area. B, Histology
of Wnt3a and BSA-treated HFs. C and D, Apoptosis detected by TUNEL and quantification of
TUNEL+ matrix cells. * p<0.05. E, Quantitative RT-PCR for p53 transcriptional targets in HF
epithelial cells in Wnt3a-treated skin. Blue star* p<0.05, compared to 0hr of BSA treatment; green
star* p<0.05, compared to 0hr of Wnt3a treatment. F and G, Pulse BrdU labeling and quantification
of K5+ BrdU+ matrix cells. Wnt3a increased K5+ cell proliferation (white arrows). * p<0.05. H,
Cyclophosphamide (CYP) treatment. Hair loss was observed 5 days after treatment. I, Wnt3a-soaked
beads (blue beads) maintained hair growth in their vicinity after CYP treatment. J, Anagen HF repair.
Depiction of cell origin and cell dynamics for early and late regenerative attempts for anagen HF
repair following IR injury. BSA: bovine serum albumin. Dashed lines in (C) (F) indicate DP. Scale
bar=75μm in (B), 25μm in (C) (F).
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Published OnlineFirst September 22, 2017.Cancer Res Wen-Yen Huang, Shih-Fan Lai, Hsien-Yi Chiu, et al. prevents hair loss from chemotherapy or radiation therapyMobilizing transit-amplifying cell-derived ectopic progenitors
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