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Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship

PURPOSE: The aim of this study was to extend current half-sarcomere models by involving a recently found force-mediated activation of the thick filament and analyze the effect of this mechanosensing regulation on the length stability of half-sarcomeres arranged in series. METHODS: We included a supe...

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Autor principal: Schappacher-Tilp, Gudrun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Shanghai University of Sport 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189248/
https://www.ncbi.nlm.nih.gov/pubmed/30356636
http://dx.doi.org/10.1016/j.jshs.2018.05.002
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author Schappacher-Tilp, Gudrun
author_facet Schappacher-Tilp, Gudrun
author_sort Schappacher-Tilp, Gudrun
collection PubMed
description PURPOSE: The aim of this study was to extend current half-sarcomere models by involving a recently found force-mediated activation of the thick filament and analyze the effect of this mechanosensing regulation on the length stability of half-sarcomeres arranged in series. METHODS: We included a super-relaxed state of myosin motors and its force-dependent activation in a conventional cross-bridge model. We simulated active stretches of a sarcomere consisting of 2 non-uniform half-sarcomeres on the descending limb of the force–length relationship. RESULTS: The mechanosensing model predicts that, in a passive sarcomere on the descending limb of the force–length relationship, the longer half-sarcomere has a higher fraction of myosin motors in the on-state than the shorter half-sarcomere. The difference in the number of myosin motors in the on-state ensures that upon calcium-mediated thin filament activation, the force-dependent thick filament activation keeps differences in active force within 20% during an active stretch. In the classical cross-bridge model, the corresponding difference exceeds 80%, leading to great length instabilities. CONCLUSION: Our simulations suggest that, in contrast to the classical cross-bridge model, the mechanosensing regulation is able to stabilize a system of non-uniform half-sarcomeres arranged in series on the descending limb of the force–length relationship.
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spelling pubmed-61892482018-10-23 Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship Schappacher-Tilp, Gudrun J Sport Health Sci Original Article PURPOSE: The aim of this study was to extend current half-sarcomere models by involving a recently found force-mediated activation of the thick filament and analyze the effect of this mechanosensing regulation on the length stability of half-sarcomeres arranged in series. METHODS: We included a super-relaxed state of myosin motors and its force-dependent activation in a conventional cross-bridge model. We simulated active stretches of a sarcomere consisting of 2 non-uniform half-sarcomeres on the descending limb of the force–length relationship. RESULTS: The mechanosensing model predicts that, in a passive sarcomere on the descending limb of the force–length relationship, the longer half-sarcomere has a higher fraction of myosin motors in the on-state than the shorter half-sarcomere. The difference in the number of myosin motors in the on-state ensures that upon calcium-mediated thin filament activation, the force-dependent thick filament activation keeps differences in active force within 20% during an active stretch. In the classical cross-bridge model, the corresponding difference exceeds 80%, leading to great length instabilities. CONCLUSION: Our simulations suggest that, in contrast to the classical cross-bridge model, the mechanosensing regulation is able to stabilize a system of non-uniform half-sarcomeres arranged in series on the descending limb of the force–length relationship. Shanghai University of Sport 2018-07 2018-05-17 /pmc/articles/PMC6189248/ /pubmed/30356636 http://dx.doi.org/10.1016/j.jshs.2018.05.002 Text en © 2018 Published by Elsevier B.V. on behalf of Shanghai University of Sport. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Schappacher-Tilp, Gudrun
Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title_full Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title_fullStr Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title_full_unstemmed Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title_short Titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
title_sort titin-mediated thick filament activation stabilizes myofibrils on the descending limb of their force–length relationship
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6189248/
https://www.ncbi.nlm.nih.gov/pubmed/30356636
http://dx.doi.org/10.1016/j.jshs.2018.05.002
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