Basic fibroblast growth factor-induced endothelial proliferation and NO synthesis involves inward rectifier K+ current

Arterioscler Thromb Vasc Biol. 2004 Jul;24(7):1229-33. doi: 10.1161/01.ATV.0000130663.37663.6a. Epub 2004 May 6.

Abstract

Objective: Inward rectifier K+ currents (K(ir)) determine the resting membrane potential and thereby modulate essential Ca2+-dependent pathways, like cell growth and synthesis of vasoactive agents in endothelial cells. Basic fibroblast growth factor (bFGF) acts as a vasodilatator and angiogenic factor. Therefore, we investigated the effect of bFGF on K(ir) and assessed the role in proliferation and nitric oxide (NO) formation of endothelial cells.

Methods and results: Using the patch-clamp technique, we found characteristic K(ir) in human umbilical cord vein endothelial cells (HUVEC), which were dose-dependently blocked by barium (10 to 100 micromol/L). Perfusion with bFGF (50 ng/mL) caused a significant increase of K(ir), which was blocked by 100 micromol/L barium (n=18, P<0.01). The bFGF-induced HUVEC proliferation was significantly inhibited when using 50 to 100 micromol/L barium (n=6; P<0.01). NO production was examined using a cGMP radioimmunoassay. bFGF caused a significant increase of cGMP levels (n=10; P<0.05), which were blocked by barium.

Conclusions: Modulation of K(ir) plays an important role in bFGF-mediated endothelial cell growth and NO formation.

MeSH terms

  • Barium / metabolism
  • Barium / pharmacology
  • Calcium / metabolism
  • Cell Division / drug effects
  • Cells, Cultured / cytology
  • Cells, Cultured / drug effects
  • Cells, Cultured / physiology
  • Cyclic GMP / biosynthesis
  • Endothelial Cells / cytology
  • Endothelial Cells / drug effects*
  • Endothelial Cells / physiology
  • Fibroblast Growth Factor 2 / pharmacology*
  • Humans
  • Ion Channel Gating / drug effects
  • Ion Channel Gating / physiology
  • Ion Transport / drug effects
  • Ion Transport / physiology
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Nitric Oxide / biosynthesis*
  • Patch-Clamp Techniques
  • Potassium / metabolism
  • Potassium Channels, Inwardly Rectifying / physiology*

Substances

  • Potassium Channels, Inwardly Rectifying
  • Fibroblast Growth Factor 2
  • Barium
  • Nitric Oxide
  • Cyclic GMP
  • Potassium
  • Calcium