VE-cadherin: at the front, center, and sides of endothelial cell organization and function

被引:232
作者
Harris, Elizabeth S. [1 ]
Nelson, W. James [1 ]
机构
[1] Stanford Univ, Dept Biol, James H Clark Ctr, Bio X Program, Stanford, CA 94305 USA
关键词
BLOOD-BRAIN-BARRIER; VASCULAR-PERMEABILITY; BETA-CATENIN; TYROSINE PHOSPHORYLATION; ADHERENS JUNCTIONS; TIGHT JUNCTIONS; GROWTH-FACTOR; IN-VIVO; DEPENDENT ENDOCYTOSIS; UP-REGULATION;
D O I
10.1016/j.ceb.2010.07.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endothelial cells form cell-cell adhesive structures, called adherens and tight junctions, which maintain tissue integrity, but must be dynamic for leukocyte transmigration during the inflammatory response and cellular remodeling during angiogenesis. This review will focus on Vascular Endothelial (VE)-cadherin, an endothelial-specific cell-cell adhesion protein of the adherens junction complex. VE-cadherin plays a key role in endothelial barrier function and angiogenesis, and consequently VE-cadherin availability and function are tightly regulated. VE-cadherin also participates directly and indirectly in intracellular signaling pathways that control cell dynamics and cell cycle progression. Here we highlight recent work that has advanced our understanding of multiple regulatory and signaling mechanisms that converge on VE-cadherin and have consequences for endothelial barrier function and angiogenic remodeling.
引用
收藏
页码:651 / 658
页数:8
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