Cargando…
Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion
Skeletal muscle stem cells, known as satellite cells (SCs), are quiescent in normal adult limb muscles. Injury stimulates SC proliferation, differentiation, and fusion to regenerate muscle structure. In pharyngeal muscles, which are critical for swallowing foods and liquids, SCs proliferate and fuse...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164287/ https://www.ncbi.nlm.nih.gov/pubmed/35669512 http://dx.doi.org/10.3389/fcell.2022.875209 |
_version_ | 1784720102514491392 |
---|---|
author | Kim, Eunhye Wu, Fang Lim, Danbi Zeuthen, Christopher Zhang, Yiming Allen, James Muraine, Laura Trollet, Capucine Vest, Katherine E. Choo, Hyojung J. |
author_facet | Kim, Eunhye Wu, Fang Lim, Danbi Zeuthen, Christopher Zhang, Yiming Allen, James Muraine, Laura Trollet, Capucine Vest, Katherine E. Choo, Hyojung J. |
author_sort | Kim, Eunhye |
collection | PubMed |
description | Skeletal muscle stem cells, known as satellite cells (SCs), are quiescent in normal adult limb muscles. Injury stimulates SC proliferation, differentiation, and fusion to regenerate muscle structure. In pharyngeal muscles, which are critical for swallowing foods and liquids, SCs proliferate and fuse in the absence of injury. It is unknown what factors drive increased basal activity of pharyngeal SCs. Here, we determined how niche factors influence the status of pharyngeal versus limb SCs. In vivo, a subset of pharyngeal SCs present features of activated SCs, including large cell size and increased mitochondrial content. In this study, we discovered that the pharyngeal muscle contains high levels of active hepatocyte growth factor (HGF), which is known to activate SCs in mice and humans. We found that fibroadipogenic progenitors (FAPs) are the major cell type providing HGF and are thus responsible for basal proliferation of SCs in pharyngeal muscles. Lastly, we confirmed the critical role of FAPs for pharyngeal muscle function and maintenance. This study gives new insights to explain the distinctive SC activity of pharyngeal muscles. |
format | Online Article Text |
id | pubmed-9164287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91642872022-06-05 Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion Kim, Eunhye Wu, Fang Lim, Danbi Zeuthen, Christopher Zhang, Yiming Allen, James Muraine, Laura Trollet, Capucine Vest, Katherine E. Choo, Hyojung J. Front Cell Dev Biol Cell and Developmental Biology Skeletal muscle stem cells, known as satellite cells (SCs), are quiescent in normal adult limb muscles. Injury stimulates SC proliferation, differentiation, and fusion to regenerate muscle structure. In pharyngeal muscles, which are critical for swallowing foods and liquids, SCs proliferate and fuse in the absence of injury. It is unknown what factors drive increased basal activity of pharyngeal SCs. Here, we determined how niche factors influence the status of pharyngeal versus limb SCs. In vivo, a subset of pharyngeal SCs present features of activated SCs, including large cell size and increased mitochondrial content. In this study, we discovered that the pharyngeal muscle contains high levels of active hepatocyte growth factor (HGF), which is known to activate SCs in mice and humans. We found that fibroadipogenic progenitors (FAPs) are the major cell type providing HGF and are thus responsible for basal proliferation of SCs in pharyngeal muscles. Lastly, we confirmed the critical role of FAPs for pharyngeal muscle function and maintenance. This study gives new insights to explain the distinctive SC activity of pharyngeal muscles. Frontiers Media S.A. 2022-05-17 /pmc/articles/PMC9164287/ /pubmed/35669512 http://dx.doi.org/10.3389/fcell.2022.875209 Text en Copyright © 2022 Kim, Wu, Lim, Zeuthen, Zhang, Allen, Muraine, Trollet, Vest and Choo. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Kim, Eunhye Wu, Fang Lim, Danbi Zeuthen, Christopher Zhang, Yiming Allen, James Muraine, Laura Trollet, Capucine Vest, Katherine E. Choo, Hyojung J. Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title | Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title_full | Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title_fullStr | Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title_full_unstemmed | Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title_short | Fibroadipogenic Progenitors Regulate the Basal Proliferation of Satellite Cells and Homeostasis of Pharyngeal Muscles via HGF Secretion |
title_sort | fibroadipogenic progenitors regulate the basal proliferation of satellite cells and homeostasis of pharyngeal muscles via hgf secretion |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9164287/ https://www.ncbi.nlm.nih.gov/pubmed/35669512 http://dx.doi.org/10.3389/fcell.2022.875209 |
work_keys_str_mv | AT kimeunhye fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT wufang fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT limdanbi fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT zeuthenchristopher fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT zhangyiming fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT allenjames fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT murainelaura fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT trolletcapucine fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT vestkatherinee fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion AT choohyojungj fibroadipogenicprogenitorsregulatethebasalproliferationofsatellitecellsandhomeostasisofpharyngealmusclesviahgfsecretion |