PDGF-dependent regulation of regulator of G protein signaling-5 expression and vascular smooth muscle cell functionality

Am J Physiol Cell Physiol. 2011 Aug;301(2):C478-89. doi: 10.1152/ajpcell.00348.2010. Epub 2011 May 18.

Abstract

Regulator of G protein signaling (RGS) proteins, and notably members of the RGS-R4 subfamily, control vasocontractility by accelerating the inactivation of Gα-dependent signaling. RGS5 is the most highly and differently expressed RGS-R4 subfamily member in arterial smooth muscle. Expression of RGS5 first appears in pericytes during development of the afferent vascular tree, suggesting that RGS5 is a good candidate for a regulator of arterial contractility and, perhaps, for determining the mass of the smooth muscle coats required to regulate blood flow in the branches of the arterial tree. Consistent with this hypothesis, using cultured vascular smooth muscle cells (VSMCs), we demonstrate RGS5 overexpression inhibits G protein-coupled receptor (GPCR)-mediated hypertrophic responses. The next objective was to determine which physiological agonists directly control RGS5 expression in VSMCs. GPCR agonists failed to directly regulate RGS5 mRNA expression; however, platelet-derived growth factor (PDGF) acutely represses expression. Downregulation of RGS5 results in the induction of migration and the activation of the GPCR-mediated signaling pathways. This stimulation leads to the activation of mitogen-activated protein kinases directly downstream of receptor stimulation, and ultimately VSMC hypertrophy. These results demonstrate that RGS5 expression is a critical mediator of both VSMC contraction and potentially, arterial remodeling.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Angiotensin II / metabolism
  • Animals
  • Becaplermin
  • Cell Line
  • Cell Movement
  • Gene Expression Regulation
  • Hypertrophy
  • Ligands
  • Mitogen-Activated Protein Kinases / metabolism
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / metabolism*
  • Myocytes, Smooth Muscle / drug effects
  • Myocytes, Smooth Muscle / metabolism*
  • Platelet-Derived Growth Factor / metabolism*
  • Proto-Oncogene Proteins c-sis
  • RGS Proteins / deficiency
  • RGS Proteins / genetics
  • RGS Proteins / metabolism*
  • RNA Interference
  • Rats
  • Receptors, G-Protein-Coupled / agonists
  • Receptors, G-Protein-Coupled / metabolism*
  • Receptors, Platelet-Derived Growth Factor / metabolism*
  • Signal Transduction* / drug effects
  • Time Factors
  • Transfection
  • Vasoconstriction

Substances

  • Ligands
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins c-sis
  • RGS Proteins
  • Receptors, G-Protein-Coupled
  • Rgs5 protein, rat
  • Angiotensin II
  • Becaplermin
  • Receptors, Platelet-Derived Growth Factor
  • Mitogen-Activated Protein Kinases