Alignment, cross linking, and beyond: a collagen architect's guide to the skeletal muscle extracellular matrix

• Published in: American Journal of Physiology: Cell Physiology Vol. 325; no. 4; pp. C1017 - C1030
• Main Authors: Wohlgemuth, Ross P, Brashear, Sarah E, Smith, Lucas R
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.10.2023
• Series: Decoding Fibrosis
• Subjects: Collagen - metabolism; Extracellular Matrix - metabolism; Fibrosis; Humans; Muscle, Skeletal - metabolism; Proteoglycans - metabolism; Review; perimysium; fibrosis; muscle matrix; collagen architecture; muscle mechanics
• ISSN: 0363-6143; 1522-1563; 1522-1563
• DOI: 10.1152/ajpcell.00287.2023

The muscle extracellular matrix (ECM) forms a complex network of collagens, proteoglycans, and other proteins that produce a favorable environment for muscle regeneration, protect the sarcolemma from contraction-induced damage, and provide a pathway for the lateral transmission of contractile force. In each of these functions, the structure and organization of the muscle ECM play an important role. Many aspects of collagen architecture, including collagen alignment, cross linking, and packing density affect the regenerative capacity, passive mechanical properties, and contractile force transmission pathways of skeletal muscle. The balance between fortifying the muscle ECM and maintaining ECM turnover and compliance is highly dependent on the integrated organization, or architecture, of the muscle matrix, especially related to collagen. While muscle ECM remodeling patterns in response to exercise and disease are similar, in that collagen synthesis can increase in both cases, one outcome leads to a stronger muscle and the other leads to fibrosis. In this review, we provide a comprehensive analysis of the architectural features of each layer of muscle ECM: epimysium, perimysium, and endomysium. Further, we detail the importance of muscle ECM architecture to biomechanical function in the context of exercise or fibrosis, including disease, injury, and aging. We describe how collagen architecture is linked to active and passive muscle biomechanics and which architectural features are acutely dynamic and adapt over time. Future studies should investigate the significance of collagen architecture in muscle stiffness, ECM turnover, and lateral force transmission in the context of health and fibrosis.