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The unified myofibrillar matrix for force generation in muscle
Human movement occurs through contraction of the basic unit of the muscle cell, the sarcomere. Sarcomeres have long been considered to be arranged end-to-end in series along the length of the muscle into tube-like myofibrils with many individual, parallel myofibrils comprising the bulk of the muscle...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381600/ https://www.ncbi.nlm.nih.gov/pubmed/32709902 http://dx.doi.org/10.1038/s41467-020-17579-6 |
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author | Willingham, T. Bradley Kim, Yuho Lindberg, Eric Bleck, Christopher K. E. Glancy, Brian |
author_facet | Willingham, T. Bradley Kim, Yuho Lindberg, Eric Bleck, Christopher K. E. Glancy, Brian |
author_sort | Willingham, T. Bradley |
collection | PubMed |
description | Human movement occurs through contraction of the basic unit of the muscle cell, the sarcomere. Sarcomeres have long been considered to be arranged end-to-end in series along the length of the muscle into tube-like myofibrils with many individual, parallel myofibrils comprising the bulk of the muscle cell volume. Here, we demonstrate that striated muscle cells form a continuous myofibrillar matrix linked together by frequently branching sarcomeres. We find that all muscle cells contain highly connected myofibrillar networks though the frequency of sarcomere branching goes down from early to late postnatal development and is higher in slow-twitch than fast-twitch mature muscles. Moreover, we show that the myofibrillar matrix is united across the entire width of the muscle cell both at birth and in mature muscle. We propose that striated muscle force is generated by a singular, mesh-like myofibrillar network rather than many individual, parallel myofibrils. |
format | Online Article Text |
id | pubmed-7381600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73816002020-07-28 The unified myofibrillar matrix for force generation in muscle Willingham, T. Bradley Kim, Yuho Lindberg, Eric Bleck, Christopher K. E. Glancy, Brian Nat Commun Article Human movement occurs through contraction of the basic unit of the muscle cell, the sarcomere. Sarcomeres have long been considered to be arranged end-to-end in series along the length of the muscle into tube-like myofibrils with many individual, parallel myofibrils comprising the bulk of the muscle cell volume. Here, we demonstrate that striated muscle cells form a continuous myofibrillar matrix linked together by frequently branching sarcomeres. We find that all muscle cells contain highly connected myofibrillar networks though the frequency of sarcomere branching goes down from early to late postnatal development and is higher in slow-twitch than fast-twitch mature muscles. Moreover, we show that the myofibrillar matrix is united across the entire width of the muscle cell both at birth and in mature muscle. We propose that striated muscle force is generated by a singular, mesh-like myofibrillar network rather than many individual, parallel myofibrils. Nature Publishing Group UK 2020-07-24 /pmc/articles/PMC7381600/ /pubmed/32709902 http://dx.doi.org/10.1038/s41467-020-17579-6 Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Willingham, T. Bradley Kim, Yuho Lindberg, Eric Bleck, Christopher K. E. Glancy, Brian The unified myofibrillar matrix for force generation in muscle |
title | The unified myofibrillar matrix for force generation in muscle |
title_full | The unified myofibrillar matrix for force generation in muscle |
title_fullStr | The unified myofibrillar matrix for force generation in muscle |
title_full_unstemmed | The unified myofibrillar matrix for force generation in muscle |
title_short | The unified myofibrillar matrix for force generation in muscle |
title_sort | unified myofibrillar matrix for force generation in muscle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381600/ https://www.ncbi.nlm.nih.gov/pubmed/32709902 http://dx.doi.org/10.1038/s41467-020-17579-6 |
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