Cargando…

Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling

Adult hair follicles undergo repeated cycling of regression (catagen), resting (telogen), and growth (anagen), which is maintained by hair follicle stem cells (HFSCs). The mechanism underlying hair growth initiation and HFSC maintenance is not fully understood. Here, by epithelial deletion of Hes1,...

Descripción completa

Detalles Bibliográficos
Autores principales: Suen, Wei‐Jeng, Li, Shao‐Ting, Yang, Liang‐Tung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027765/
https://www.ncbi.nlm.nih.gov/pubmed/31721388
http://dx.doi.org/10.1002/stem.3117
_version_ 1783498901987262464
author Suen, Wei‐Jeng
Li, Shao‐Ting
Yang, Liang‐Tung
author_facet Suen, Wei‐Jeng
Li, Shao‐Ting
Yang, Liang‐Tung
author_sort Suen, Wei‐Jeng
collection PubMed
description Adult hair follicles undergo repeated cycling of regression (catagen), resting (telogen), and growth (anagen), which is maintained by hair follicle stem cells (HFSCs). The mechanism underlying hair growth initiation and HFSC maintenance is not fully understood. Here, by epithelial deletion of Hes1, a major Notch downstream transcriptional repressor, we found that hair growth is retarded, but the hair cycle progresses normally. Hes1 is specifically upregulated in the lower bulge/HG during anagen initiation. Accordingly, loss of Hes1 results in delayed activation of the secondary hair germ (HG) and shortened anagen phase. This developmental delay causes reduced hair shaft length but not identity changes in follicular lineages. Remarkably, Hes1 ablation results in impaired hair regeneration upon repetitive depilation. Microarray gene profiling on HFSCs indicates that Hes1 modulates Shh responsiveness in anagen initiation. Using primary keratinocyte cultures, we demonstrated that Hes1 deletion negatively influences ciliogenesis and Smoothened ciliary accumulation upon Shh treatment. Furthermore, transient application of Smoothened agonist during repetitive depilation can rescue anagen initiation and HFSC self‐renewal in Hes1‐deficient hair follicles. We reveal a critical function of Hes1 in potentiating Shh signaling in anagen initiation, which allows sufficient signaling strength to expand the HG and replenish HFSCs to maintain the hair cycle homeostasis.
format Online
Article
Text
id pubmed-7027765
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley & Sons, Inc.
record_format MEDLINE/PubMed
spelling pubmed-70277652020-02-24 Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling Suen, Wei‐Jeng Li, Shao‐Ting Yang, Liang‐Tung Stem Cells Tissue‐specific Stem Cells Adult hair follicles undergo repeated cycling of regression (catagen), resting (telogen), and growth (anagen), which is maintained by hair follicle stem cells (HFSCs). The mechanism underlying hair growth initiation and HFSC maintenance is not fully understood. Here, by epithelial deletion of Hes1, a major Notch downstream transcriptional repressor, we found that hair growth is retarded, but the hair cycle progresses normally. Hes1 is specifically upregulated in the lower bulge/HG during anagen initiation. Accordingly, loss of Hes1 results in delayed activation of the secondary hair germ (HG) and shortened anagen phase. This developmental delay causes reduced hair shaft length but not identity changes in follicular lineages. Remarkably, Hes1 ablation results in impaired hair regeneration upon repetitive depilation. Microarray gene profiling on HFSCs indicates that Hes1 modulates Shh responsiveness in anagen initiation. Using primary keratinocyte cultures, we demonstrated that Hes1 deletion negatively influences ciliogenesis and Smoothened ciliary accumulation upon Shh treatment. Furthermore, transient application of Smoothened agonist during repetitive depilation can rescue anagen initiation and HFSC self‐renewal in Hes1‐deficient hair follicles. We reveal a critical function of Hes1 in potentiating Shh signaling in anagen initiation, which allows sufficient signaling strength to expand the HG and replenish HFSCs to maintain the hair cycle homeostasis. John Wiley & Sons, Inc. 2019-11-26 2020-02 /pmc/articles/PMC7027765/ /pubmed/31721388 http://dx.doi.org/10.1002/stem.3117 Text en ©2019 The Authors. stem cells published by Wiley Periodicals, Inc. on behalf of AlphaMed Press 2019 This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Tissue‐specific Stem Cells
Suen, Wei‐Jeng
Li, Shao‐Ting
Yang, Liang‐Tung
Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title_full Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title_fullStr Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title_full_unstemmed Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title_short Hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
title_sort hes1 regulates anagen initiation and hair follicle regeneration through modulation of hedgehog signaling
topic Tissue‐specific Stem Cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027765/
https://www.ncbi.nlm.nih.gov/pubmed/31721388
http://dx.doi.org/10.1002/stem.3117
work_keys_str_mv AT suenweijeng hes1regulatesanageninitiationandhairfollicleregenerationthroughmodulationofhedgehogsignaling
AT lishaoting hes1regulatesanageninitiationandhairfollicleregenerationthroughmodulationofhedgehogsignaling
AT yangliangtung hes1regulatesanageninitiationandhairfollicleregenerationthroughmodulationofhedgehogsignaling