PUBLICATION

Rap1 promotes VEGFR2 activation and angiogenesis by a mechanism involving integrin alpha v beta 3

Authors
Lakshmikanthan, S., Sobczak, M., Chun, C., Henschel, A., Dargatz, J., Ramchandran, R., and Chrzanowska-Wodnicka, M.
ID
ZDB-PUB-110609-57
Date
2011
Source
Blood   118(7): 2015-26 (Journal)
Registered Authors
Chun, Chang Zoon, Ramchandran, Ramani
Keywords
none
MeSH Terms
  • Animals
  • Cells, Cultured
  • Down-Regulation
  • Endothelial Cells/cytology
  • Endothelial Cells/metabolism
  • Gene Deletion
  • Integrin alphaVbeta3/metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Neovascularization, Physiologic*
  • Vascular Endothelial Growth Factor Receptor-2/metabolism*
  • Zebrafish
  • rap GTP-Binding Proteins/genetics
  • rap GTP-Binding Proteins/metabolism
  • rap1 GTP-Binding Proteins/genetics
  • rap1 GTP-Binding Proteins/metabolism*
PubMed
21636859 Full text @ Blood
Abstract

Vascular Endothelial Growth Factor (VEGF) acting through Vascular Endothelial Growth Factor Receptor 2 (VEGFR2) on endothelial cells (ECs) is a key regulator of angiogenesis, a process essential for wound healing and tumor metastasis. Rap1a and Rap1b, two highly homologous small G proteins are both required for angiogenesis in vivo and for normal EC responses to VEGF. Here we sought to determine the mechanism through which Rap1 promotes VEGF-mediated angiogenesis. Using lineage-restricted Rap1-knockout mice we show that Rap1-deficiency in endothelium leads to defective angiogenesis in vivo, in a dose-dependent manner. Using ECs obtained from Rap1-deficient mice we demonstrate that Rap1b promotes VEGF-VEGFR2 kinase activation and regulates integrin activation. Importantly, the Rap1b-dependent VEGF-VEGFR2 activation is in part mediated via integrin αvβ3. Further, in an in vivo model of zebrafish angiogenesis, we demonstrate that Rap1b is essential for the sprouting of intersomitic vessels, a process known to be dependent on VEGF-signaling. Using two distinct pharmacological VEGFR2 inhibitors we show that Rap1b and VEGFR2 act additively to control angiogenesis in vivo. We conclude that Rap1b promotes VEGF-mediated angiogenesis by promoting VEGFR2 activation in ECs via integrin αvβ3. These results provide a novel insight into the role of Rap1 in VEGF signaling in ECs.

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