Activation of receptor-mediated angiogenesis and signaling pathways after VEGF administration in fetal rat CNS explants

J Cereb Blood Flow Metab. 2003 Dec;23(12):1420-9. doi: 10.1097/01.WCB.0000090620.86921.9C.

Abstract

The angiogenic role of vascular endothelial growth factor (VEGF) receptors, flk-1 and flt-1, and their downstream signaling pathways, MAPK/ERK and PI-3 kinase, were examined in a fetal rat cortical explant model after exposure to exogenous VEGF. Treatment with VEGF resulted in substantial neovascularization characterized by increased vascular flk-1 receptor expression, whereas flt-1 receptor protein expression was absent. The specific role of flk-1 receptors in the angiogenic process was confirmed by the addition of antisense oligonucleotides (AS-ODNs) to flk-1, which blocked angiogenesis, whereas AS-ODNs to flt-1 had no effect. These results were further supported by the finding that specific chemical inhibition of flk-1 receptors caused disruption of the angiogenic response, whereas inhibition of the flt-1 receptors had no effect. Application of either MAPK/ERK or PI-3 kinase pathway inhibitors disrupted VEGF-induced angiogenesis, thereby indicating that both signaling pathways mediate this process. Thus VEGF binding to the endothelial flk-1 receptor activates the MAPK/ERK and PI-3 kinase pathways, resulting in neoangiogenic events. Of interest is the fact that although VEGF is regarded as a vascular permeability factor, its application to nascent cortical tissue caused an increase in a key physiologic protein of the blood-brain barrier function, glucose transporter-1, suggesting that the cytokine may have a role in blood-brain barrier development.

Publication types

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

MeSH terms

  • Animals
  • Blood-Brain Barrier / physiology
  • Brain Tissue Transplantation*
  • Cells, Cultured
  • Endothelium, Vascular / metabolism
  • Female
  • Fetal Tissue Transplantation*
  • Glucose Transporter Type 1
  • MAP Kinase Signaling System / drug effects
  • MAP Kinase Signaling System / physiology*
  • Monosaccharide Transport Proteins / metabolism
  • Neovascularization, Physiologic / drug effects
  • Neovascularization, Physiologic / physiology*
  • Neurons / cytology
  • Neurons / transplantation
  • Pregnancy
  • Rats
  • Rats, Wistar
  • Vascular Endothelial Growth Factor A / pharmacology*
  • Vascular Endothelial Growth Factor Receptor-2 / antagonists & inhibitors
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism

Substances

  • Glucose Transporter Type 1
  • Monosaccharide Transport Proteins
  • Slc2a1 protein, rat
  • Vascular Endothelial Growth Factor A
  • Vascular Endothelial Growth Factor Receptor-2