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Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise
Satellite cells are required for postnatal development, skeletal muscle regeneration across the lifespan, and skeletal muscle hypertrophy prior to maturity. Our group has aimed to address whether satellite cells are required for hypertrophic growth in mature skeletal muscle. Here, we generated a com...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179974/ https://www.ncbi.nlm.nih.gov/pubmed/34109314 http://dx.doi.org/10.1093/function/zqaa033 |
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author | Englund, Davis A Figueiredo, Vandré C Dungan, Cory M Murach, Kevin A Peck, Bailey D Petrosino, Jennifer M Brightwell, Camille R Dupont, Alec M Neal, Ally C Fry, Christopher S Accornero, Federica McCarthy, John J Peterson, Charlotte A |
author_facet | Englund, Davis A Figueiredo, Vandré C Dungan, Cory M Murach, Kevin A Peck, Bailey D Petrosino, Jennifer M Brightwell, Camille R Dupont, Alec M Neal, Ally C Fry, Christopher S Accornero, Federica McCarthy, John J Peterson, Charlotte A |
author_sort | Englund, Davis A |
collection | PubMed |
description | Satellite cells are required for postnatal development, skeletal muscle regeneration across the lifespan, and skeletal muscle hypertrophy prior to maturity. Our group has aimed to address whether satellite cells are required for hypertrophic growth in mature skeletal muscle. Here, we generated a comprehensive characterization and transcriptome-wide profiling of skeletal muscle during adaptation to exercise in the presence or absence of satellite cells in order to identify distinct phenotypes and gene networks influenced by satellite cell content. We administered vehicle or tamoxifen to adult Pax7-DTA mice and subjected them to progressive weighted wheel running (PoWeR). We then performed immunohistochemical analysis and whole-muscle RNA-seq of vehicle (SC+) and tamoxifen-treated (SC−) mice. Further, we performed single myonuclear RNA-seq to provide detailed information on how satellite cell fusion affects myonuclear transcription. We show that while skeletal muscle can mount a robust hypertrophic response to PoWeR in the absence of satellite cells, growth, and adaptation are ultimately blunted. Transcriptional profiling reveals several gene networks key to muscle adaptation are altered in the absence of satellite cells. |
format | Online Article Text |
id | pubmed-8179974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81799742021-06-07 Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise Englund, Davis A Figueiredo, Vandré C Dungan, Cory M Murach, Kevin A Peck, Bailey D Petrosino, Jennifer M Brightwell, Camille R Dupont, Alec M Neal, Ally C Fry, Christopher S Accornero, Federica McCarthy, John J Peterson, Charlotte A Function (Oxf) Original Research Satellite cells are required for postnatal development, skeletal muscle regeneration across the lifespan, and skeletal muscle hypertrophy prior to maturity. Our group has aimed to address whether satellite cells are required for hypertrophic growth in mature skeletal muscle. Here, we generated a comprehensive characterization and transcriptome-wide profiling of skeletal muscle during adaptation to exercise in the presence or absence of satellite cells in order to identify distinct phenotypes and gene networks influenced by satellite cell content. We administered vehicle or tamoxifen to adult Pax7-DTA mice and subjected them to progressive weighted wheel running (PoWeR). We then performed immunohistochemical analysis and whole-muscle RNA-seq of vehicle (SC+) and tamoxifen-treated (SC−) mice. Further, we performed single myonuclear RNA-seq to provide detailed information on how satellite cell fusion affects myonuclear transcription. We show that while skeletal muscle can mount a robust hypertrophic response to PoWeR in the absence of satellite cells, growth, and adaptation are ultimately blunted. Transcriptional profiling reveals several gene networks key to muscle adaptation are altered in the absence of satellite cells. Oxford University Press 2020-11-23 /pmc/articles/PMC8179974/ /pubmed/34109314 http://dx.doi.org/10.1093/function/zqaa033 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of American Physiological Society. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Original Research Englund, Davis A Figueiredo, Vandré C Dungan, Cory M Murach, Kevin A Peck, Bailey D Petrosino, Jennifer M Brightwell, Camille R Dupont, Alec M Neal, Ally C Fry, Christopher S Accornero, Federica McCarthy, John J Peterson, Charlotte A Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title | Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title_full | Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title_fullStr | Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title_full_unstemmed | Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title_short | Satellite Cell Depletion Disrupts Transcriptional Coordination and Muscle Adaptation to Exercise |
title_sort | satellite cell depletion disrupts transcriptional coordination and muscle adaptation to exercise |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8179974/ https://www.ncbi.nlm.nih.gov/pubmed/34109314 http://dx.doi.org/10.1093/function/zqaa033 |
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