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Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle
Skeletal muscle adaptations to exercise have been associated with a range of health-related benefits, but cell type-specific adaptations within the muscle are incompletely understood. Here we use single-cell sequencing to determine the effects of exercise on cellular composition and cell type-specif...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588010/ https://www.ncbi.nlm.nih.gov/pubmed/36273106 http://dx.doi.org/10.1038/s42003-022-04088-z |
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author | Lovrić, Alen Rassolie, Ali Alam, Seher Mandić, Mirko Saini, Amarjit Altun, Mikael Fernandez-Gonzalo, Rodrigo Gustafsson, Thomas Rullman, Eric |
author_facet | Lovrić, Alen Rassolie, Ali Alam, Seher Mandić, Mirko Saini, Amarjit Altun, Mikael Fernandez-Gonzalo, Rodrigo Gustafsson, Thomas Rullman, Eric |
author_sort | Lovrić, Alen |
collection | PubMed |
description | Skeletal muscle adaptations to exercise have been associated with a range of health-related benefits, but cell type-specific adaptations within the muscle are incompletely understood. Here we use single-cell sequencing to determine the effects of exercise on cellular composition and cell type-specific processes in human skeletal muscle before and after intense exercise. Fifteen clusters originating from six different cell populations were identified. Most cell populations remained quantitatively stable after exercise, but a large transcriptional response was observed in mesenchymal, endothelial, and myogenic cells, suggesting that these cells are specifically involved in skeletal muscle remodeling. We found three subpopulations of myogenic cells characterized by different maturation stages based on the expression of markers such as PAX7, MYOD1, TNNI1, and TNNI2. Exercise accelerated the trajectory of myogenic progenitor cells towards maturation by increasing the transcriptional features of fast- and slow-twitch muscle fibers. The transcriptional regulation of these contractile elements upon differentiation was validated in vitro on primary myoblast cells. The cell type-specific adaptive mechanisms induced by exercise presented here contribute to the understanding of the skeletal muscle adaptations triggered by physical activity and may ultimately have implications for physiological and pathological processes affecting skeletal muscle, such as sarcopenia, cachexia, and glucose homeostasis. |
format | Online Article Text |
id | pubmed-9588010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95880102022-10-24 Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle Lovrić, Alen Rassolie, Ali Alam, Seher Mandić, Mirko Saini, Amarjit Altun, Mikael Fernandez-Gonzalo, Rodrigo Gustafsson, Thomas Rullman, Eric Commun Biol Article Skeletal muscle adaptations to exercise have been associated with a range of health-related benefits, but cell type-specific adaptations within the muscle are incompletely understood. Here we use single-cell sequencing to determine the effects of exercise on cellular composition and cell type-specific processes in human skeletal muscle before and after intense exercise. Fifteen clusters originating from six different cell populations were identified. Most cell populations remained quantitatively stable after exercise, but a large transcriptional response was observed in mesenchymal, endothelial, and myogenic cells, suggesting that these cells are specifically involved in skeletal muscle remodeling. We found three subpopulations of myogenic cells characterized by different maturation stages based on the expression of markers such as PAX7, MYOD1, TNNI1, and TNNI2. Exercise accelerated the trajectory of myogenic progenitor cells towards maturation by increasing the transcriptional features of fast- and slow-twitch muscle fibers. The transcriptional regulation of these contractile elements upon differentiation was validated in vitro on primary myoblast cells. The cell type-specific adaptive mechanisms induced by exercise presented here contribute to the understanding of the skeletal muscle adaptations triggered by physical activity and may ultimately have implications for physiological and pathological processes affecting skeletal muscle, such as sarcopenia, cachexia, and glucose homeostasis. Nature Publishing Group UK 2022-10-22 /pmc/articles/PMC9588010/ /pubmed/36273106 http://dx.doi.org/10.1038/s42003-022-04088-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lovrić, Alen Rassolie, Ali Alam, Seher Mandić, Mirko Saini, Amarjit Altun, Mikael Fernandez-Gonzalo, Rodrigo Gustafsson, Thomas Rullman, Eric Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title | Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title_full | Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title_fullStr | Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title_full_unstemmed | Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title_short | Single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
title_sort | single-cell sequencing deconvolutes cellular responses to exercise in human skeletal muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9588010/ https://www.ncbi.nlm.nih.gov/pubmed/36273106 http://dx.doi.org/10.1038/s42003-022-04088-z |
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