Ena/VASP is required for endothelial barrier function in vivo

被引:91
作者
Furman, Craig
Sieminski, Alisha L.
Kwiatkowski, Adam V.
Rubinson, Douglas A.
Vasile, Eliza
Bronson, Roderick T.
Faessler, Reinhard
Gertler, Frank B. [1 ]
机构
[1] MIT, Ctr Canc Res, Cambridge, MA 02139 USA
[2] Franklin W Olin Coll Engn, Dept Bioengn, Needham, MA 02492 USA
[3] Harvard Med Sch, Dept Pathol, Boston, MA 02115 USA
[4] Max Planck Inst Biochem, Dept Mol Med, D-82157 Martinsried, Germany
[5] Pfizer Res Technol Ctr, Cambridge, MA 02139 USA
[6] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
关键词
D O I
10.1083/jcb.200705002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
引用
收藏
页码:761 / 775
页数:15
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