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Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training.

Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training.
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 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.
2045-2322
Willis, Craig R.G.
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Deane, Colleen S.
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Ames, Ryan M.
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Bass, Joseph J.
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Wilkinson, Daniel J.
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Smith, Kenneth
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Phillips, Bethan E.
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Szewczyk, Nathaniel J.
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Atherton, Philip J.
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Etheridge, Timothy
b835c46c-bb14-44ab-bd68-08a03943c1a3
Willis, Craig R.G.
66ff4d21-e206-458b-94ec-b4f829dc9727
Deane, Colleen S.
3320532e-f411-4ea8-9a14-4a9f248da898
Ames, Ryan M.
b4509923-155a-4026-88f0-9e116ece7f0f
Bass, Joseph J.
e93cd462-0593-4ef4-9088-c23cf42ef1e5
Wilkinson, Daniel J.
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Smith, Kenneth
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Phillips, Bethan E.
311cbf08-ee74-4841-9e7e-6a96ce5049d1
Szewczyk, Nathaniel J.
e0310853-8847-46b8-8694-50d248af114d
Atherton, Philip J.
c777bf46-a14b-420b-9278-d5935acd818f
Etheridge, Timothy
b835c46c-bb14-44ab-bd68-08a03943c1a3

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. and Etheridge, Timothy (2021) Transcriptomic adaptation during skeletal muscle habituation to eccentric or concentric exercise training. Scientific Reports, 11, [23930]. (doi:10.1038/s41598-021-03393-7).

Record type: Article

Abstract

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.

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Accepted/In Press date: 19 November 2021
e-pub ahead of print date: 14 December 2021

Identifiers

Local EPrints ID: 483343
URI: http://eprints.soton.ac.uk/id/eprint/483343
ISSN: 2045-2322
PURE UUID: a9a88639-6125-4e5a-b131-7370f9ea0050
ORCID for Colleen S. Deane: ORCID iD orcid.org/0000-0002-2281-6479

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Date deposited: 30 Oct 2023 07:57
Last modified: 17 Mar 2024 04:15

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Contributors

Author: Craig R.G. Willis
Author: Colleen S. Deane ORCID iD
Author: Ryan M. Ames
Author: Joseph J. Bass
Author: Daniel J. Wilkinson
Author: Kenneth Smith
Author: Bethan E. Phillips
Author: Nathaniel J. Szewczyk
Author: Philip J. Atherton
Author: Timothy Etheridge

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