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Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing
Mammalian wounds typically heal by fibrotic repair without hair follicle (HF) regeneration. Fibrosis and regeneration are currently considered the opposite end of wound healing. This study sought to determine if scar could be remodeled to promote healing with HF regeneration. Here, we identify that...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249328/ https://www.ncbi.nlm.nih.gov/pubmed/30464171 http://dx.doi.org/10.1038/s41467-018-07142-9 |
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author | Lim, Chae Ho Sun, Qi Ratti, Karan Lee, Soung-Hoon Zheng, Ying Takeo, Makoto Lee, Wendy Rabbani, Piul Plikus, Maksim V. Cain, Jason E. Wang, David H. Watkins, D. Neil Millar, Sarah Taketo, M. Mark Myung, Peggy Cotsarelis, George Ito, Mayumi |
author_facet | Lim, Chae Ho Sun, Qi Ratti, Karan Lee, Soung-Hoon Zheng, Ying Takeo, Makoto Lee, Wendy Rabbani, Piul Plikus, Maksim V. Cain, Jason E. Wang, David H. Watkins, D. Neil Millar, Sarah Taketo, M. Mark Myung, Peggy Cotsarelis, George Ito, Mayumi |
author_sort | Lim, Chae Ho |
collection | PubMed |
description | Mammalian wounds typically heal by fibrotic repair without hair follicle (HF) regeneration. Fibrosis and regeneration are currently considered the opposite end of wound healing. This study sought to determine if scar could be remodeled to promote healing with HF regeneration. Here, we identify that activation of the Sonic hedgehog (Shh) pathway reinstalls a regenerative dermal niche, called dermal papilla, which is required and sufficient for HF neogenesis (HFN). Epidermal Shh overexpression or constitutive Smoothened dermal activation results in extensive HFN in wounds that otherwise end in scarring. While long-term Wnt activation is associated with fibrosis, Shh signal activation in Wnt active cells promotes the dermal papilla fate in scarring wounds. These studies demonstrate that mechanisms of scarring and regeneration are not distant from one another and that wound repair can be redirected to promote regeneration following injury by modifying a key dermal signal. |
format | Online Article Text |
id | pubmed-6249328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62493282018-11-26 Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing Lim, Chae Ho Sun, Qi Ratti, Karan Lee, Soung-Hoon Zheng, Ying Takeo, Makoto Lee, Wendy Rabbani, Piul Plikus, Maksim V. Cain, Jason E. Wang, David H. Watkins, D. Neil Millar, Sarah Taketo, M. Mark Myung, Peggy Cotsarelis, George Ito, Mayumi Nat Commun Article Mammalian wounds typically heal by fibrotic repair without hair follicle (HF) regeneration. Fibrosis and regeneration are currently considered the opposite end of wound healing. This study sought to determine if scar could be remodeled to promote healing with HF regeneration. Here, we identify that activation of the Sonic hedgehog (Shh) pathway reinstalls a regenerative dermal niche, called dermal papilla, which is required and sufficient for HF neogenesis (HFN). Epidermal Shh overexpression or constitutive Smoothened dermal activation results in extensive HFN in wounds that otherwise end in scarring. While long-term Wnt activation is associated with fibrosis, Shh signal activation in Wnt active cells promotes the dermal papilla fate in scarring wounds. These studies demonstrate that mechanisms of scarring and regeneration are not distant from one another and that wound repair can be redirected to promote regeneration following injury by modifying a key dermal signal. Nature Publishing Group UK 2018-11-21 /pmc/articles/PMC6249328/ /pubmed/30464171 http://dx.doi.org/10.1038/s41467-018-07142-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Lim, Chae Ho Sun, Qi Ratti, Karan Lee, Soung-Hoon Zheng, Ying Takeo, Makoto Lee, Wendy Rabbani, Piul Plikus, Maksim V. Cain, Jason E. Wang, David H. Watkins, D. Neil Millar, Sarah Taketo, M. Mark Myung, Peggy Cotsarelis, George Ito, Mayumi Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title | Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title_full | Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title_fullStr | Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title_full_unstemmed | Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title_short | Hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
title_sort | hedgehog stimulates hair follicle neogenesis by creating inductive dermis during murine skin wound healing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6249328/ https://www.ncbi.nlm.nih.gov/pubmed/30464171 http://dx.doi.org/10.1038/s41467-018-07142-9 |
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