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Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training
Eccentric (ECC) and concentric (CON) contractions induce distinct muscle remodelling patterns that manifest early during exercise training, the causes of which remain unclear. We examined molecular signatures of early contraction mode-specific muscle adaptation via transcriptome-wide network and sec...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671437/ https://www.ncbi.nlm.nih.gov/pubmed/34907264 http://dx.doi.org/10.1038/s41598-021-03393-7 |
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author | Willis, Craig R. G. Deane, Colleen S. Ames, Ryan M. Bass, Joseph J. Wilkinson, Daniel J. Smith, Kenneth Phillips, Bethan E. Szewczyk, Nathaniel J. Atherton, Philip J. Etheridge, Timothy |
author_facet | Willis, Craig R. G. Deane, Colleen S. Ames, Ryan M. Bass, Joseph J. Wilkinson, Daniel J. Smith, Kenneth Phillips, Bethan E. Szewczyk, Nathaniel J. Atherton, Philip J. Etheridge, Timothy |
author_sort | Willis, Craig R. G. |
collection | PubMed |
description | Eccentric (ECC) and concentric (CON) contractions induce distinct muscle remodelling patterns that manifest early during exercise training, the causes of which remain unclear. We examined molecular signatures of early contraction mode-specific muscle adaptation via transcriptome-wide network and secretome analyses during 2 weeks of ECC- versus CON-specific (downhill versus uphill running) exercise training (exercise ‘habituation’). Despite habituation attenuating total numbers of exercise-induced genes, functional gene-level profiles of untrained ECC or CON were largely unaltered post-habituation. Network analysis revealed 11 ECC-specific modules, including upregulated extracellular matrix and immune profiles plus downregulated mitochondrial pathways following untrained ECC. Of 3 CON-unique modules, 2 were ribosome-related and downregulated post-habituation. Across training, 376 ECC-specific and 110 CON-specific hub genes were identified, plus 45 predicted transcription factors. Secreted factors were enriched in 3 ECC- and/or CON-responsive modules, with all 3 also being under the predicted transcriptional control of SP1 and KLF4. Of 34 candidate myokine hubs, 1 was also predicted to have elevated expression in skeletal muscle versus other tissues: THBS4, of a secretome-enriched module upregulated after untrained ECC. In conclusion, distinct untrained ECC and CON transcriptional responses are dampened after habituation without substantially shifting molecular functional profiles, providing new mechanistic candidates into contraction-mode specific muscle regulation. |
format | Online Article Text |
id | pubmed-8671437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86714372021-12-16 Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training Willis, Craig R. G. Deane, Colleen S. Ames, Ryan M. Bass, Joseph J. Wilkinson, Daniel J. Smith, Kenneth Phillips, Bethan E. Szewczyk, Nathaniel J. Atherton, Philip J. Etheridge, Timothy Sci Rep Article Eccentric (ECC) and concentric (CON) contractions induce distinct muscle remodelling patterns that manifest early during exercise training, the causes of which remain unclear. We examined molecular signatures of early contraction mode-specific muscle adaptation via transcriptome-wide network and secretome analyses during 2 weeks of ECC- versus CON-specific (downhill versus uphill running) exercise training (exercise ‘habituation’). Despite habituation attenuating total numbers of exercise-induced genes, functional gene-level profiles of untrained ECC or CON were largely unaltered post-habituation. Network analysis revealed 11 ECC-specific modules, including upregulated extracellular matrix and immune profiles plus downregulated mitochondrial pathways following untrained ECC. Of 3 CON-unique modules, 2 were ribosome-related and downregulated post-habituation. Across training, 376 ECC-specific and 110 CON-specific hub genes were identified, plus 45 predicted transcription factors. Secreted factors were enriched in 3 ECC- and/or CON-responsive modules, with all 3 also being under the predicted transcriptional control of SP1 and KLF4. Of 34 candidate myokine hubs, 1 was also predicted to have elevated expression in skeletal muscle versus other tissues: THBS4, of a secretome-enriched module upregulated after untrained ECC. In conclusion, distinct untrained ECC and CON transcriptional responses are dampened after habituation without substantially shifting molecular functional profiles, providing new mechanistic candidates into contraction-mode specific muscle regulation. Nature Publishing Group UK 2021-12-14 /pmc/articles/PMC8671437/ /pubmed/34907264 http://dx.doi.org/10.1038/s41598-021-03393-7 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Willis, Craig R. G. Deane, Colleen S. Ames, Ryan M. Bass, Joseph J. Wilkinson, Daniel J. Smith, Kenneth Phillips, Bethan E. Szewczyk, Nathaniel J. Atherton, Philip J. Etheridge, Timothy Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title | Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title_full | Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title_fullStr | Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title_full_unstemmed | Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title_short | Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
title_sort | transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671437/ https://www.ncbi.nlm.nih.gov/pubmed/34907264 http://dx.doi.org/10.1038/s41598-021-03393-7 |
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