Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Willingham, T. Bradley, Kim, Yuho, Lindberg, Eric, Bleck, Christopher K. E., Glancy, Brian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
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
_version_ 1783563077236555776
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
work_keys_str_mv AT willinghamtbradley theunifiedmyofibrillarmatrixforforcegenerationinmuscle
AT kimyuho theunifiedmyofibrillarmatrixforforcegenerationinmuscle
AT lindbergeric theunifiedmyofibrillarmatrixforforcegenerationinmuscle
AT bleckchristopherke theunifiedmyofibrillarmatrixforforcegenerationinmuscle
AT glancybrian theunifiedmyofibrillarmatrixforforcegenerationinmuscle
AT willinghamtbradley unifiedmyofibrillarmatrixforforcegenerationinmuscle
AT kimyuho unifiedmyofibrillarmatrixforforcegenerationinmuscle
AT lindbergeric unifiedmyofibrillarmatrixforforcegenerationinmuscle
AT bleckchristopherke unifiedmyofibrillarmatrixforforcegenerationinmuscle
AT glancybrian unifiedmyofibrillarmatrixforforcegenerationinmuscle