Rasip1 is required for endothelial cell motility, angiogenesis and vessel formation

Ke Xu, Diana C. Chong, Scott A. Rankin, Aaron M. Zorn, Ondine Cleaver

Research output: Contribution to journalArticle

43 Scopus citations

Abstract

Ras proteins are small GTPases that regulate cellular growth and differentiation. Components of the Ras signaling pathway have been shown to be important during embryonic vasculogenesis and angiogenesis. Here, we report that Rasip1, which encodes a novel Ras-interacting protein, is strongly expressed in vascular endothelial cells throughout development, in both mouse and frog. Similar to the well-characterized vascular markers VEGFR2 and PECAM, Rasip1 is specifically expressed in angioblasts prior to vessel formation, in the initial embryonic vascular plexus, in the growing blood vessels during angiogenesis and in the endothelium of mature blood vessels into the postnatal period. Rasip1 expression is undetectable in VEGFR2 null embryos, which lack endothelial cells, suggesting that Rasip1 is endothelial specific. siRNA-mediated reduction of Rasip1 severely impairs angiogenesis and motility in endothelial cell cultures, and morpholino knockdown experiments in frog embryos demonstrate that Rasip1 is required for embryonic vessel formation in vivo. Together, these data identify Rasip1 as a novel endothelial factor that plays an essential role in vascular development.

Original languageEnglish (US)
Pages (from-to)269-279
Number of pages11
JournalDevelopmental Biology
Volume329
Issue number2
DOIs
StatePublished - May 15 2009

Keywords

  • Angiogenesis
  • Blood vessel
  • Endothelium
  • Flk-1
  • Migration
  • Proliferation
  • Ras
  • Rasip1
  • VEGFR2
  • Vasculogenesis

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology

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