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Early satellite cell communication creates a permissive environment for long-term muscle growth
Using in vivo muscle stem cell (satellite cell)-specific extracellular vesicle (EV) tracking, satellite cell depletion, in vitro cell culture, and single-cell RNA sequencing, we show satellite cells communicate with other cells in skeletal muscle during mechanical overload. Early satellite cell EV c...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080523/ https://www.ncbi.nlm.nih.gov/pubmed/33948557 http://dx.doi.org/10.1016/j.isci.2021.102372 |
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author | Murach, Kevin A. Peck, Bailey D. Policastro, Robert A. Vechetti, Ivan J. Van Pelt, Douglas W. Dungan, Cory M. Denes, Lance T. Fu, Xu Brightwell, Camille R. Zentner, Gabriel E. Dupont-Versteegden, Esther E. Richards, Christopher I. Smith, Jeramiah J. Fry, Christopher S. McCarthy, John J. Peterson, Charlotte A. |
author_facet | Murach, Kevin A. Peck, Bailey D. Policastro, Robert A. Vechetti, Ivan J. Van Pelt, Douglas W. Dungan, Cory M. Denes, Lance T. Fu, Xu Brightwell, Camille R. Zentner, Gabriel E. Dupont-Versteegden, Esther E. Richards, Christopher I. Smith, Jeramiah J. Fry, Christopher S. McCarthy, John J. Peterson, Charlotte A. |
author_sort | Murach, Kevin A. |
collection | PubMed |
description | Using in vivo muscle stem cell (satellite cell)-specific extracellular vesicle (EV) tracking, satellite cell depletion, in vitro cell culture, and single-cell RNA sequencing, we show satellite cells communicate with other cells in skeletal muscle during mechanical overload. Early satellite cell EV communication primes the muscle milieu for proper long-term extracellular matrix (ECM) deposition and is sufficient to support sustained hypertrophy in adult mice, even in the absence of fusion to muscle fibers. Satellite cells modulate chemokine gene expression across cell types within the first few days of loading, and EV delivery of miR-206 to fibrogenic cells represses Wisp1 expression required for appropriate ECM remodeling. Late-stage communication from myogenic cells during loading is widespread but may be targeted toward endothelial cells. Satellite cells coordinate adaptation by influencing the phenotype of recipient cells, which extends our understanding of their role in muscle adaptation beyond regeneration and myonuclear donation. |
format | Online Article Text |
id | pubmed-8080523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80805232021-05-03 Early satellite cell communication creates a permissive environment for long-term muscle growth Murach, Kevin A. Peck, Bailey D. Policastro, Robert A. Vechetti, Ivan J. Van Pelt, Douglas W. Dungan, Cory M. Denes, Lance T. Fu, Xu Brightwell, Camille R. Zentner, Gabriel E. Dupont-Versteegden, Esther E. Richards, Christopher I. Smith, Jeramiah J. Fry, Christopher S. McCarthy, John J. Peterson, Charlotte A. iScience Article Using in vivo muscle stem cell (satellite cell)-specific extracellular vesicle (EV) tracking, satellite cell depletion, in vitro cell culture, and single-cell RNA sequencing, we show satellite cells communicate with other cells in skeletal muscle during mechanical overload. Early satellite cell EV communication primes the muscle milieu for proper long-term extracellular matrix (ECM) deposition and is sufficient to support sustained hypertrophy in adult mice, even in the absence of fusion to muscle fibers. Satellite cells modulate chemokine gene expression across cell types within the first few days of loading, and EV delivery of miR-206 to fibrogenic cells represses Wisp1 expression required for appropriate ECM remodeling. Late-stage communication from myogenic cells during loading is widespread but may be targeted toward endothelial cells. Satellite cells coordinate adaptation by influencing the phenotype of recipient cells, which extends our understanding of their role in muscle adaptation beyond regeneration and myonuclear donation. Elsevier 2021-03-29 /pmc/articles/PMC8080523/ /pubmed/33948557 http://dx.doi.org/10.1016/j.isci.2021.102372 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Murach, Kevin A. Peck, Bailey D. Policastro, Robert A. Vechetti, Ivan J. Van Pelt, Douglas W. Dungan, Cory M. Denes, Lance T. Fu, Xu Brightwell, Camille R. Zentner, Gabriel E. Dupont-Versteegden, Esther E. Richards, Christopher I. Smith, Jeramiah J. Fry, Christopher S. McCarthy, John J. Peterson, Charlotte A. Early satellite cell communication creates a permissive environment for long-term muscle growth |
title | Early satellite cell communication creates a permissive environment for long-term muscle growth |
title_full | Early satellite cell communication creates a permissive environment for long-term muscle growth |
title_fullStr | Early satellite cell communication creates a permissive environment for long-term muscle growth |
title_full_unstemmed | Early satellite cell communication creates a permissive environment for long-term muscle growth |
title_short | Early satellite cell communication creates a permissive environment for long-term muscle growth |
title_sort | early satellite cell communication creates a permissive environment for long-term muscle growth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080523/ https://www.ncbi.nlm.nih.gov/pubmed/33948557 http://dx.doi.org/10.1016/j.isci.2021.102372 |
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