Interactive role of tyrosine kinase, protein kinase C, and Rho/Rho kinase systems in the mechanotransduction of vascular smooth muscles

Biorheology. 2003;40(1-3):307-14.

Abstract

Blood vessels are always subjected to hemodynamic stresses including blood pressure and blood flow. The cerebral artery is particularly sensitive to hemodynamic stresses such as pressure and stretch, and shows contractions that are myogenic in nature; i.e., the mechanical response is generated by the vascular smooth muscle itself. The artery constricts in response to an increase in intraluminal pressure, and dilates in response to a decrease in the intraluminal pressure. We provide herein some insights into the mechanotransduction of vascular tissue; i.e., we discuss how the tissue is receptive to mechanical force and how the latter induces the specific signals leading to myogenic contraction in terms of mechanosensor action and subsequent intracellular signaling. The interactive role of tyrosine kinase, protein kinase C, and Rho/Rho-kinase systems in the mechanotransduction process is discussed, which systems also seem to play an important role in the development of experimental cerebral vasospasm. The study of the mechanotransduction in vascular tissue may aid in clarifying the mechanisms underlying vasospastic episodes and pathologic remodeling in cardiovascular diseases, and may potentially have therapeutic consequences.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Cerebral Arteries / physiology
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Mechanotransduction, Cellular / physiology*
  • Muscle Contraction / physiology*
  • Muscle, Smooth, Vascular / enzymology*
  • Muscle, Smooth, Vascular / physiology
  • Protein Kinase C / physiology*
  • Protein Serine-Threonine Kinases / physiology
  • Protein-Tyrosine Kinases / physiology*
  • Stress, Mechanical
  • rho-Associated Kinases

Substances

  • Intracellular Signaling Peptides and Proteins
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases
  • rho-Associated Kinases
  • Protein Kinase C