| Literature DB >> 25752958 |
Hiroyuki Yamamoto1, Manuel Ehling1, Katsuhiro Kato1, Kenichi Kanai1, Max van Lessen1, Maike Frye2, Dagmar Zeuschner3, Masanori Nakayama1, Dietmar Vestweber2, Ralf H Adams1.
Abstract
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.Entities:
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Year: 2015 PMID: 25752958 DOI: 10.1038/ncomms7429
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919