<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Willingham TB</submitter><funding>Intramural NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Heart, Lung, and Blood Institute</funding><pagination>3722</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7381600</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>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 </pubmed_abstract><journal>Nature communications</journal><pubmed_title>The unified myofibrillar matrix for force generation in muscle.</pubmed_title><pmcid>PMC7381600</pmcid><funding_grant_id>1ZIAHL006221-03</funding_grant_id><funding_grant_id>ZIA HL006221</funding_grant_id><pubmed_authors>Willingham TB</pubmed_authors><pubmed_authors>Kim Y</pubmed_authors><pubmed_authors>Bleck CKE</pubmed_authors><pubmed_authors>Glancy B</pubmed_authors><pubmed_authors>Lindberg E</pubmed_authors></additional><is_claimable>false</is_claimable><name>The unified myofibrillar matrix for force generation in muscle.</name><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 </description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-06T19:41:12.29Z</modification><creation>2025-04-06T19:41:12.29Z</creation></dates><accession>S-EPMC7381600</accession><cross_references><pubmed>32709902</pubmed><doi>10.1038/s41467-020-17579-6</doi></cross_references></HashMap>