Stretch-induced contractile differentiation of vascular smooth muscle: sensitivity to actin polymerization inhibitors

Am J Physiol Cell Physiol. 2003 Jun;284(6):C1387-96. doi: 10.1152/ajpcell.00508.2002. Epub 2003 Jan 29.

Abstract

Signaling mechanisms for stretch-dependent growth and differentiation of vascular smooth muscle were investigated in mechanically loaded rat portal veins in organ culture. Stretch-dependent protein synthesis was found to depend on endogenous release of angiotensin II. Autoradiography after [(35)S]methionine incorporation revealed stretch-dependent synthesis of several proteins, of which SM22 and actin were particularly prominent. Inhibition of RhoA activity by cell-permeant C3 toxin increased tissue mechanical compliance and reduced stretch-dependent extracellular signal-regulated kinase (ERK)1/2 activation, growth, and synthesis of actin and SM22, suggesting a role of the actin cytoskeleton. In contrast, inhibition of Rho-associated kinase by Y-27632 did not reduce ERK1/2 phosphorylation or actin and SM22 synthesis and did not affect tissue mechanical compliance but still inhibited overall growth. The actin polymerization inhibitors latrunculin B and cytochalasin D both inhibited growth and caused increased tissue compliance. Whereas latrunculin B concentration-dependently reduced actin and SM22 synthesis, cytochalasin D did so at low (10(-8) M) but not at high (10(-6) M) concentration. The results show that stretch stabilizes the contractile smooth muscle phenotype. Stretch-dependent differentiation marker expression requires an intact cytoskeleton for stretch sensing, control of protein expression via the level of unpolymerized G-actin, or both.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Actins / metabolism*
  • Angiotensin II / metabolism
  • Animals
  • Bridged Bicyclo Compounds, Heterocyclic / metabolism
  • Cell Differentiation / physiology*
  • Culture Techniques
  • Cytochalasin D / metabolism
  • Cytoskeleton / metabolism
  • Enzyme Activation
  • Enzyme Inhibitors / metabolism*
  • Female
  • MAP Kinase Signaling System / physiology
  • Microfilament Proteins / metabolism
  • Muscle Contraction / physiology*
  • Muscle Proteins / metabolism
  • Muscle, Smooth, Vascular / physiology*
  • Nucleic Acid Synthesis Inhibitors / metabolism
  • Portal Vein
  • Rats
  • Rats, Sprague-Dawley
  • Stress, Mechanical
  • Thiazoles / metabolism
  • Thiazolidines
  • rhoA GTP-Binding Protein / metabolism

Substances

  • Actins
  • Bridged Bicyclo Compounds, Heterocyclic
  • Enzyme Inhibitors
  • Microfilament Proteins
  • Muscle Proteins
  • Nucleic Acid Synthesis Inhibitors
  • Tagln protein, mouse
  • Thiazoles
  • Thiazolidines
  • transgelin
  • Angiotensin II
  • Cytochalasin D
  • rhoA GTP-Binding Protein
  • latrunculin B