The unified myofibrillar matrix for force generation in muscle

• Published in: Nature communications 2020-07, Vol.11 (1), p.3722-3722, Article 3722
• Main Authors: Willingham, T. Bradley, Kim, Yuho, Lindberg, Eric, Bleck, Christopher K. E., Glancy, Brian
• Format: Article
• Language: English
• Subjects: 14/28; 631/443; 631/535/1258; 692/698/1671/1668/1973; Cell size; Contraction; Human motion; Humanities and Social Sciences; multidisciplinary; Muscle contraction; Muscles; Musculoskeletal system; Myofibrils; Sarcomeres; Scanning electron microscopy; Science; Science (multidisciplinary); Skeletal muscle
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-020-17579-6

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. Skeletal muscle cells have long been considered to be made primarily of many individual, parallel myofibrils. Here, the authors show that the striated muscle contractile machinery forms a highly branched, mesh-like myofibrillar matrix connected across the entire length and width of the muscle cell.