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Integrin β1 controls VE-cadherin localization and blood vessel stability.

Hiroyuki YamamotoManuel EhlingKatsuhiro KatoKenichi KanaiMax van LessenMaike FryeDagmar ZeuschnerMasanori NakayamaDietmar VestweberRalf H Adams
Published in: Nature communications (2015)
Angiogenic blood vessel growth requires several distinct but integrated cellular activities. Endothelial cell sprouting and proliferation lead to the expansion of the vasculature and give rise to a highly branched, immature plexus, which is subsequently reorganized into a mature and stable network. Although it is known that integrin-mediated cell-matrix interactions are indispensable for embryonic angiogenesis, little is known about the function of integrins in different steps of vascular morphogenesis. Here, by investigating the integrin β1-subunit with inducible and endothelial-specific gene targeting in the postnatal mouse retina, we show that β1 integrin promotes endothelial sprouting but is a negative regulator of proliferation. In maturing vessels, integrin β1 is indispensable for proper localization of VE-cadherin and thereby cell-cell junction integrity. The sum of our findings establishes that integrin β1 has critical functions in the growing and maturing vasculature, and is required for the formation of stable, non-leaky blood vessels.
Keyphrases
  • cell adhesion
  • endothelial cells
  • cell migration
  • single cell
  • cell therapy
  • signaling pathway
  • mesenchymal stem cells
  • genome wide
  • drug delivery