4.8 Article

Integrin β1 controls VE-cadherin localization and blood vessel stability

Journal

NATURE COMMUNICATIONS
Volume 6, Issue -, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms7429

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Funding

  1. Max Planck Society
  2. University of Munster
  3. Deutsche Forschungsgemeinschaft [SFB 629]
  4. EMBO Long-Term Fellowship program

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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 beta 1-subunit with inducible and endothelial-specific gene targeting in the postnatal mouse retina, we show that beta 1 integrin promotes endothelial sprouting but is a negative regulator of proliferation. In maturing vessels, integrin beta 1 is indispensable for proper localization of VE-cadherin and thereby cell-cell junction integrity. The sum of our findings establishes that integrin beta 1 has critical functions in the growing and maturing vasculature, and is required for the formation of stable, non-leaky blood vessels.

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