Caveolin-1 regulates contractility in differentiated vascular smooth muscle

Am J Physiol Heart Circ Physiol. 2004 Jan;286(1):H91-8. doi: 10.1152/ajpheart.00472.2003. Epub 2003 Sep 11.

Abstract

Caveolin is a principal component of caveolar membranes. In the present study, we utilized a decoy peptide approach to define the degree of involvement of caveolin in PKC-dependent regulation of contractility of differentiated vascular smooth muscle. The primary isoform of caveolin in ferret aorta vascular smooth muscle is caveolin-1. Chemical loading of contractile vascular smooth muscle tissue with a synthetic caveolin-1 scaffolding domain peptide inhibited PKC-dependent increases in contractility induced by a phorbol ester or an alpha agonist. Peptide loading also resulted in a significant inhibition of phorbol ester-induced adducin Ser662 phosphorylation, an intracellular monitor of PKC kinase activity, ERK1/2 activation, and Ser789 phosphorylation of the actin binding protein caldesmon. alpha-Agonist-induced ERK1-1/2 activation was also inhibited by the caveolin-1 peptide. Scrambled peptide-loaded tissues or sham-loaded tissues were unaffected with respect to both contractility and signaling. Depolarization-induced activation of contraction was not affected by caveolin peptide loading. Similar results with respect to contractility and ERK1/2 activation during exposure to the phorbol ester or the alpha-agonist were obtained with the cholesterol-depleting agent methyl-beta-cyclodextrin. These results are consistent with a role for caveolin-1 in the coordination of signaling leading to the regulation of contractility of smooth muscle.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Anticholesteremic Agents / pharmacology
  • Aorta / metabolism
  • Calmodulin-Binding Proteins / metabolism
  • Calmodulin-Binding Proteins / pharmacology
  • Caveolin 1
  • Caveolins / pharmacology
  • Caveolins / physiology*
  • Ferrets
  • Mitogen-Activated Protein Kinases / metabolism
  • Muscle, Smooth, Vascular / physiology*
  • Peptide Fragments / pharmacology
  • Phorbol Esters / pharmacology
  • Phosphorylation
  • Protein Kinase C / metabolism
  • Vasoconstriction / drug effects
  • Vasoconstriction / physiology*

Substances

  • Anticholesteremic Agents
  • Calmodulin-Binding Proteins
  • Caveolin 1
  • Caveolins
  • Peptide Fragments
  • Phorbol Esters
  • 12-deoxyphorbol-13-isobutyrate-20-acetate
  • Protein Kinase C
  • Mitogen-Activated Protein Kinases