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Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle
Recent X-ray diffraction studies on actively contracting fibres from skeletal muscle showed that the number of myosin motors available to interact with actin-containing thin filaments is controlled by the stress in the myosin-containing thick filaments. Those results suggested that thick filament me...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095582/ https://www.ncbi.nlm.nih.gov/pubmed/27796302 http://dx.doi.org/10.1038/ncomms13281 |
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author | Fusi, L. Brunello, E. Yan, Z. Irving, M. |
author_facet | Fusi, L. Brunello, E. Yan, Z. Irving, M. |
author_sort | Fusi, L. |
collection | PubMed |
description | Recent X-ray diffraction studies on actively contracting fibres from skeletal muscle showed that the number of myosin motors available to interact with actin-containing thin filaments is controlled by the stress in the myosin-containing thick filaments. Those results suggested that thick filament mechano-sensing might constitute a novel regulatory mechanism in striated muscles that acts independently of the well-known thin filament-mediated calcium signalling pathway. Here we test that hypothesis using probes attached to the myosin regulatory light chain in demembranated muscle fibres. We show that both the extent and kinetics of thick filament activation depend on thick filament stress but are independent of intracellular calcium concentration in the physiological range. These results establish direct control of myosin motors by thick filament mechano-sensing as a general regulatory mechanism in skeletal muscle that is independent of the canonical calcium signalling pathway. |
format | Online Article Text |
id | pubmed-5095582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-50955822016-11-18 Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle Fusi, L. Brunello, E. Yan, Z. Irving, M. Nat Commun Article Recent X-ray diffraction studies on actively contracting fibres from skeletal muscle showed that the number of myosin motors available to interact with actin-containing thin filaments is controlled by the stress in the myosin-containing thick filaments. Those results suggested that thick filament mechano-sensing might constitute a novel regulatory mechanism in striated muscles that acts independently of the well-known thin filament-mediated calcium signalling pathway. Here we test that hypothesis using probes attached to the myosin regulatory light chain in demembranated muscle fibres. We show that both the extent and kinetics of thick filament activation depend on thick filament stress but are independent of intracellular calcium concentration in the physiological range. These results establish direct control of myosin motors by thick filament mechano-sensing as a general regulatory mechanism in skeletal muscle that is independent of the canonical calcium signalling pathway. Nature Publishing Group 2016-10-31 /pmc/articles/PMC5095582/ /pubmed/27796302 http://dx.doi.org/10.1038/ncomms13281 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Fusi, L. Brunello, E. Yan, Z. Irving, M. Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title | Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title_full | Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title_fullStr | Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title_full_unstemmed | Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title_short | Thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
title_sort | thick filament mechano-sensing is a calcium-independent regulatory mechanism in skeletal muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5095582/ https://www.ncbi.nlm.nih.gov/pubmed/27796302 http://dx.doi.org/10.1038/ncomms13281 |
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