Tubulin acetylation increases cytoskeletal stiffness to regulate mechanotransduction in striated muscle

J Gen Physiol. 2021 Jul 5;153(7):e202012743. doi: 10.1085/jgp.202012743.

Abstract

Microtubules tune cytoskeletal stiffness, which affects cytoskeletal mechanics and mechanotransduction of striated muscle. While recent evidence suggests that microtubules enriched in detyrosinated α-tubulin regulate these processes in healthy muscle and increase them in disease, the possible contribution from several other α-tubulin modifications has not been investigated. Here, we used genetic and pharmacologic strategies in isolated cardiomyocytes and skeletal myofibers to increase the level of acetylated α-tubulin without altering the level of detyrosinated α-tubulin. We show that microtubules enriched in acetylated α-tubulin increase cytoskeletal stiffness and viscoelastic resistance. These changes slow rates of contraction and relaxation during unloaded contraction and increased activation of NADPH oxidase 2 (Nox2) by mechanotransduction. Together, these findings add to growing evidence that microtubules contribute to the mechanobiology of striated muscle in health and disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Mechanotransduction, Cellular
  • Microtubules / metabolism
  • Muscle, Striated* / metabolism
  • Tubulin* / metabolism
  • Tyrosine / metabolism

Substances

  • Tubulin
  • Tyrosine