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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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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Shanghai University of Sport
2018
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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. |
format | Online Article Text |
id | pubmed-6189248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Shanghai University of Sport |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT schappachertilpgudrun titinmediatedthickfilamentactivationstabilizesmyofibrilsonthedescendinglimboftheirforcelengthrelationship |