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Excitation-Contraction Coupling Alterations in Myopathies

During the complex series of events leading to muscle contraction, the initial electric signal coming from motor neurons is transformed into an increase in calcium concentration that triggers sliding of myofibrils. This process, referred to as excitation–contraction coupling, is reliant upon the cal...

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Detalles Bibliográficos
Autores principales: Marty, Isabelle, Fauré, Julien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240595/
https://www.ncbi.nlm.nih.gov/pubmed/27911331
http://dx.doi.org/10.3233/JND-160172
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author Marty, Isabelle
Fauré, Julien
author_facet Marty, Isabelle
Fauré, Julien
author_sort Marty, Isabelle
collection PubMed
description During the complex series of events leading to muscle contraction, the initial electric signal coming from motor neurons is transformed into an increase in calcium concentration that triggers sliding of myofibrils. This process, referred to as excitation–contraction coupling, is reliant upon the calcium-release complex, which is restricted spatially to a sub-compartment of muscle cells (“the triad”) and regulated precisely. Any dysfunction in the calcium-release complex leads to muscle impairment and myopathy. Various causes can lead to alterations in excitation–contraction coupling and to muscle diseases. The latter are reviewed and classified into four categories: (i) mutation in a protein of the calcium-release complex; (ii) alteration in triad structure; (iii) modification of regulation of channels; (iv) modification in calcium stores within the muscle. Current knowledge of the pathophysiologic mechanisms in each category is described and discussed.
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spelling pubmed-52405952017-01-23 Excitation-Contraction Coupling Alterations in Myopathies Marty, Isabelle Fauré, Julien J Neuromuscul Dis Review During the complex series of events leading to muscle contraction, the initial electric signal coming from motor neurons is transformed into an increase in calcium concentration that triggers sliding of myofibrils. This process, referred to as excitation–contraction coupling, is reliant upon the calcium-release complex, which is restricted spatially to a sub-compartment of muscle cells (“the triad”) and regulated precisely. Any dysfunction in the calcium-release complex leads to muscle impairment and myopathy. Various causes can lead to alterations in excitation–contraction coupling and to muscle diseases. The latter are reviewed and classified into four categories: (i) mutation in a protein of the calcium-release complex; (ii) alteration in triad structure; (iii) modification of regulation of channels; (iv) modification in calcium stores within the muscle. Current knowledge of the pathophysiologic mechanisms in each category is described and discussed. IOS Press 2016-11-29 /pmc/articles/PMC5240595/ /pubmed/27911331 http://dx.doi.org/10.3233/JND-160172 Text en IOS Press and the authors. All rights reserved https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Marty, Isabelle
Fauré, Julien
Excitation-Contraction Coupling Alterations in Myopathies
title Excitation-Contraction Coupling Alterations in Myopathies
title_full Excitation-Contraction Coupling Alterations in Myopathies
title_fullStr Excitation-Contraction Coupling Alterations in Myopathies
title_full_unstemmed Excitation-Contraction Coupling Alterations in Myopathies
title_short Excitation-Contraction Coupling Alterations in Myopathies
title_sort excitation-contraction coupling alterations in myopathies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5240595/
https://www.ncbi.nlm.nih.gov/pubmed/27911331
http://dx.doi.org/10.3233/JND-160172
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