Ena/VASP is required for endothelial barrier function in vivo

Craig Furman, Alisha L. Sieminski, Adam V. Kwiatkowski, Douglas A. Rubinson, Eliza Vasile, Roderick T. Bronson, Reinhard Fässler, Frank B. Gertler

Research output: Contribution to journalArticlepeer-review

96 Scopus citations

Abstract

Enabled/vasodilator-stimulated phosphoprotein (Ena/VASP) proteins are key actin regulators that localize at regions of dynamic actin remodeling, including cellular protrusions and cell-cell and cell-matrix junctions. Several studies have suggested that Ena/VASP proteins are involved in the formation and function of cellular junctions. Here, we establish the importance of Ena/VASP in endothelial junctions in vivo by analysis of Ena/VASP-deficient animals. In the absence of Ena/VASP, the vasculature exhibits patterning defects and lacks structural integrity, leading to edema, hemorrhaging, and late stage embryonic lethality. In endothelial cells, we find that Ena/VASP activity is required for normal F-actin content, actomyosin contractility, and proper response to shear stress. These findings demonstrate that Ena/VASP is critical for actin cytoskeleton remodeling events involved in the maintenance of functional endothelia.

Original languageEnglish
Pages (from-to)761-775
Number of pages15
JournalJournal of Cell Biology
Volume179
Issue number4
DOIs
StatePublished - 19 Nov 2007
Externally publishedYes

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