Endothelial Alpha-Parvin Controls Integrity of Developing Vasculature and Is Required for Maintenance of Cell–Cell Junctions

RATIONALE:Angiogenesis and vessel integrity depend on the adhesion of endothelial cells (ECs) to the extracellular matrix and to adjacent ECs. The focal adhesion protein α-parvin (α-pv) is essential for vascular development. However, the role of α-pv in ECs in vivo is not known. OBJECTIVE:To determi...

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Veröffentlicht in:Circulation research 2015-06, Vol.117 (1), p.29-40
Hauptverfasser: Fraccaroli, Alessia, Pitter, Bettina, Taha, Abdallah Abu, Seebach, Jochen, Huveneers, Stephan, Kirsch, Julian, Casaroli-Marano, Ricardo P, Zahler, Stefan, Pohl, Ulrich, Gerhardt, Holger, Schnittler, Hans-J, Montanez, Eloi
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Sprache:eng
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Zusammenfassung:RATIONALE:Angiogenesis and vessel integrity depend on the adhesion of endothelial cells (ECs) to the extracellular matrix and to adjacent ECs. The focal adhesion protein α-parvin (α-pv) is essential for vascular development. However, the role of α-pv in ECs in vivo is not known. OBJECTIVE:To determine the function of α-pv in ECs during vascular development in vivo and the underlying mechanisms. METHODS AND RESULTS:We deleted the α-pv gene specifically in ECs of mice to study its role in angiogenesis and vascular development. Here, we show that endothelial-specific deletion of α-pv in mice results in late embryonic lethality associated with hemorrhages and reduced vascular density. Postnatal-induced EC-specific deletion of α-pv leads to retinal hypovascularization because of reduced vessel sprouting and excessive vessel regression. In the absence of α-pv, blood vessels display impaired VE-cadherin junction morphology. In vitro, α-pv–deficient ECs show reduced stable adherens junctions, decreased monolayer formation, and impaired motility, associated with reduced formation of integrin-mediated cell–extracellular matrix adhesion structures and an altered actin cytoskeleton. CONCLUSIONS:Endothelial α-pv is essential for vessel sprouting and for vessel stability.
ISSN:0009-7330
1524-4571
DOI:10.1161/CIRCRESAHA.117.305818