Stiffness anisotropy coordinates supracellular contractility driving long-range myotube-ECM alignment

• Published in: Science advances Vol. 10; no. 22; p. eadn0235
• Main Authors: Skillin, Nathaniel P, Kirkpatrick, Bruce E, Herbert, Katie M, Nelson, Benjamin R, Hach, Grace K, Günay, Kemal Arda, Khan, Ryan M, DelRio, Frank W, White, Timothy J, Anseth, Kristi S
• Format: Journal Article
• Language: English
• Published: United States AAAS 31.05.2024
• Subjects: Animals; Anisotropy; Cell Differentiation; Cell Line; Extracellular Matrix; Mice; Muscle Contraction - physiology; Muscle Fibers, Skeletal - physiology; Myoblasts - cytology; Science & Technology - Other Topics
• ISSN: 2375-2548; 2375-2548
• DOI: 10.1126/sciadv.adn0235

The ability of cells to organize into tissues with proper structure and function requires the effective coordination of proliferation, migration, polarization, and differentiation across length scales. Skeletal muscle is innately anisotropic; however, few biomaterials can emulate mechanical anisotropy to determine its influence on tissue patterning without introducing confounding topography. Here, we demonstrate that substrate stiffness anisotropy coordinates contractility-driven collective cellular dynamics resulting in C2C12 myotube alignment over millimeter-scale distances. When cultured on mechanically anisotropic liquid crystalline polymer networks (LCNs) lacking topography, C2C12 myoblasts collectively polarize in the stiffest direction. Cellular coordination is amplified through reciprocal cell-ECM dynamics that emerge during fusion, driving global myotube-ECM ordering. Conversely, myotube alignment was restricted to small local domains with no directional preference on mechanically isotropic LCNs of the same chemical formulation. These findings provide valuable insights for designing biomaterials that mimic anisotropic microenvironments and underscore the importance of stiffness anisotropy in orchestrating tissue morphogenesis.