Cargando…
Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock
Tissue growth in the adult is an orchestrated process that often requires biological clocks to time stem cell and progenitor activity. Here, we employed the hair follicle, which cycles between growth and regression in a timely-restricted mode, to show that some components of the hair cycle clock res...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547083/ https://www.ncbi.nlm.nih.gov/pubmed/33037205 http://dx.doi.org/10.1038/s41467-020-18643-x |
_version_ | 1783592358901710848 |
---|---|
author | Harshuk-Shabso, Sarina Dressler, Hila Niehrs, Christof Aamar, Emil Enshell-Seijffers, David |
author_facet | Harshuk-Shabso, Sarina Dressler, Hila Niehrs, Christof Aamar, Emil Enshell-Seijffers, David |
author_sort | Harshuk-Shabso, Sarina |
collection | PubMed |
description | Tissue growth in the adult is an orchestrated process that often requires biological clocks to time stem cell and progenitor activity. Here, we employed the hair follicle, which cycles between growth and regression in a timely-restricted mode, to show that some components of the hair cycle clock reside within the mesenchymal niche of the hair follicle, the dermal papilla (DP), and both Fgf and Wnt signaling pathways interact within the DP to regulate the expression of these components that include Wnt agonists (Rspondins) and antagonists (Dkk2 and Notum). The levels of Wnt agonists and antagonists in the DP are progressively reduced and elevated during the growth phase, respectively. Consequently, Wnt signaling activity in the overlying epithelial progenitor cells decreases, resulting in the induction of the regression phase. Remarkably, DP properties allow Wnt activity in the DP to persist despite the Wnt-inhibiting milieu and consequently synchronize the induction and progression of the regression phase. This study provides insight into the importance of signaling crosstalk in coupling progenitors and their niche to regulate tissue growth. |
format | Online Article Text |
id | pubmed-7547083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75470832020-10-19 Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock Harshuk-Shabso, Sarina Dressler, Hila Niehrs, Christof Aamar, Emil Enshell-Seijffers, David Nat Commun Article Tissue growth in the adult is an orchestrated process that often requires biological clocks to time stem cell and progenitor activity. Here, we employed the hair follicle, which cycles between growth and regression in a timely-restricted mode, to show that some components of the hair cycle clock reside within the mesenchymal niche of the hair follicle, the dermal papilla (DP), and both Fgf and Wnt signaling pathways interact within the DP to regulate the expression of these components that include Wnt agonists (Rspondins) and antagonists (Dkk2 and Notum). The levels of Wnt agonists and antagonists in the DP are progressively reduced and elevated during the growth phase, respectively. Consequently, Wnt signaling activity in the overlying epithelial progenitor cells decreases, resulting in the induction of the regression phase. Remarkably, DP properties allow Wnt activity in the DP to persist despite the Wnt-inhibiting milieu and consequently synchronize the induction and progression of the regression phase. This study provides insight into the importance of signaling crosstalk in coupling progenitors and their niche to regulate tissue growth. Nature Publishing Group UK 2020-10-09 /pmc/articles/PMC7547083/ /pubmed/33037205 http://dx.doi.org/10.1038/s41467-020-18643-x Text en © The Author(s) 2020 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 Harshuk-Shabso, Sarina Dressler, Hila Niehrs, Christof Aamar, Emil Enshell-Seijffers, David Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title | Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title_full | Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title_fullStr | Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title_full_unstemmed | Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title_short | Fgf and Wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
title_sort | fgf and wnt signaling interaction in the mesenchymal niche regulates the murine hair cycle clock |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7547083/ https://www.ncbi.nlm.nih.gov/pubmed/33037205 http://dx.doi.org/10.1038/s41467-020-18643-x |
work_keys_str_mv | AT harshukshabsosarina fgfandwntsignalinginteractioninthemesenchymalnicheregulatesthemurinehaircycleclock AT dresslerhila fgfandwntsignalinginteractioninthemesenchymalnicheregulatesthemurinehaircycleclock AT niehrschristof fgfandwntsignalinginteractioninthemesenchymalnicheregulatesthemurinehaircycleclock AT aamaremil fgfandwntsignalinginteractioninthemesenchymalnicheregulatesthemurinehaircycleclock AT enshellseijffersdavid fgfandwntsignalinginteractioninthemesenchymalnicheregulatesthemurinehaircycleclock |