Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise

Abstract High-force eccentric exercise results in sustained increases in cytoplasmic Ca2+ levels ([Ca2+]cyto), which can cause damage to the muscle. Here we report that a heavy-load strength training bout greatly alters the structure of the membrane network inside the fibres, the tubular (t-) system...

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Main Authors: Tanya R. Cully, Robyn M. Murphy, Llion Roberts, Truls Raastad, Robert G. Fassett, Jeff S. Coombes, Izzy Jayasinghe, Bradley S. Launikonis
Format: Article
Language:English
Published: Nature Portfolio 2017-02-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/ncomms14266
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author Tanya R. Cully
Robyn M. Murphy
Llion Roberts
Truls Raastad
Robert G. Fassett
Jeff S. Coombes
Izzy Jayasinghe
Bradley S. Launikonis
author_facet Tanya R. Cully
Robyn M. Murphy
Llion Roberts
Truls Raastad
Robert G. Fassett
Jeff S. Coombes
Izzy Jayasinghe
Bradley S. Launikonis
author_sort Tanya R. Cully
collection DOAJ
description Abstract High-force eccentric exercise results in sustained increases in cytoplasmic Ca2+ levels ([Ca2+]cyto), which can cause damage to the muscle. Here we report that a heavy-load strength training bout greatly alters the structure of the membrane network inside the fibres, the tubular (t-) system, causing the loss of its predominantly transverse organization and an increase in vacuolation of its longitudinal tubules across adjacent sarcomeres. The transverse tubules and vacuoles displayed distinct Ca2+-handling properties. Both t-system components could take up Ca2+ from the cytoplasm but only transverse tubules supported store-operated Ca2+ entry. The retention of significant amounts of Ca2+ within vacuoles provides an effective mechanism to reduce the total content of Ca2+ within the fibre cytoplasm. We propose this ability can reduce or limit resistance exercise-induced, Ca2+-dependent damage to the fibre by the reduction of [Ca2+]cyto to help maintain fibre viability during the period associated with delayed onset muscle soreness.
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spelling doaj.art-ac5dc5c88c904369b9a94eb7648f2c362023-07-02T11:20:49ZengNature PortfolioNature Communications2041-17232017-02-018111010.1038/ncomms14266Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exerciseTanya R. Cully0Robyn M. Murphy1Llion Roberts2Truls Raastad3Robert G. Fassett4Jeff S. Coombes5Izzy Jayasinghe6Bradley S. Launikonis7School of Biomedical Sciences, The University of QueenslandDepartment of Biochemistry & Genetics, La Trobe Institute for Molecular Science, La Trobe UniversitySchool of Human Movement and Nutritional Sciences, The University of QueenslandNorwegian School of Sport SciencesSchool of Human Movement and Nutritional Sciences, The University of QueenslandSchool of Human Movement and Nutritional Sciences, The University of QueenslandSchool of Biomedical Sciences, The University of QueenslandSchool of Biomedical Sciences, The University of QueenslandAbstract High-force eccentric exercise results in sustained increases in cytoplasmic Ca2+ levels ([Ca2+]cyto), which can cause damage to the muscle. Here we report that a heavy-load strength training bout greatly alters the structure of the membrane network inside the fibres, the tubular (t-) system, causing the loss of its predominantly transverse organization and an increase in vacuolation of its longitudinal tubules across adjacent sarcomeres. The transverse tubules and vacuoles displayed distinct Ca2+-handling properties. Both t-system components could take up Ca2+ from the cytoplasm but only transverse tubules supported store-operated Ca2+ entry. The retention of significant amounts of Ca2+ within vacuoles provides an effective mechanism to reduce the total content of Ca2+ within the fibre cytoplasm. We propose this ability can reduce or limit resistance exercise-induced, Ca2+-dependent damage to the fibre by the reduction of [Ca2+]cyto to help maintain fibre viability during the period associated with delayed onset muscle soreness.https://doi.org/10.1038/ncomms14266
spellingShingle Tanya R. Cully
Robyn M. Murphy
Llion Roberts
Truls Raastad
Robert G. Fassett
Jeff S. Coombes
Izzy Jayasinghe
Bradley S. Launikonis
Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
Nature Communications
title Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
title_full Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
title_fullStr Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
title_full_unstemmed Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
title_short Human skeletal muscle plasmalemma alters its structure to change its Ca2+-handling following heavy-load resistance exercise
title_sort human skeletal muscle plasmalemma alters its structure to change its ca2 handling following heavy load resistance exercise
url https://doi.org/10.1038/ncomms14266
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