Vascular endothelial growth factor receptor-2 induces survival of hematopoietic progenitor cells

J Biol Chem. 2003 Jun 13;278(24):22006-13. doi: 10.1074/jbc.M212158200. Epub 2003 Mar 30.

Abstract

Vascular endothelial growth factor (VEGF) and its receptors play an essential role in the formation and maintenance of the hematopoietic and vascular compartments. The VEGF receptor-2 (VEGFR-2) is expressed on a population of hematopoietic cells, although its role in hematopoiesis is still unclear. In this report, we have utilized a strategy to selectively activate VEGFR-2 and study its effects in primary bone marrow cells. We found that VEGFR-2 can maintain the hematopoietic progenitor population in mouse bone marrow cultured in the absence of exogenous cytokines. Maintenance of the hematopoietic progenitor population is due to increased cell survival with minimal effect on proliferation. Progenitor survival is mainly mediated by activation of the phosphatidylinositol 3'-kinase/Akt pathway. Although VEGFR-2 also activated Erk1/2 mitogen-activated protein kinase, it did not induce cell proliferation, and blockade of this pathway only partially decreased VEGFR-2-mediated survival of hematopoietic progenitors. Thus, the role of VEGFR-2 in hematopoiesis is likely to maintain survival of hematopoietic progenitors through the activation of antiapoptotic pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Apoptosis
  • Bone Marrow Cells / cytology
  • Cell Division
  • Cell Line
  • Cell Survival
  • Cytokines / metabolism
  • Dimerization
  • Genetic Vectors
  • Hematopoietic Stem Cells / metabolism*
  • Immunoblotting
  • MAP Kinase Signaling System
  • Mice
  • Microscopy, Fluorescence
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Plasmids / metabolism
  • Protein Binding
  • Recombinant Fusion Proteins / metabolism
  • Retroviridae / genetics
  • Stem Cells
  • Time Factors
  • Vascular Endothelial Growth Factor Receptor-2 / metabolism*

Substances

  • Cytokines
  • Recombinant Fusion Proteins
  • Phosphatidylinositol 3-Kinases
  • Vascular Endothelial Growth Factor Receptor-2
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases