Vascular Endothelial (VE)-Cadherin, Endothelial Adherens Junctions, and Vascular Disease

被引:93
|
作者
Lampugnani, Maria Grazia [1 ,2 ]
Dejana, Elisabetta [1 ,3 ]
Giampietro, Costanza [1 ]
机构
[1] Inst Mol Oncol, FIRC, I-20139 Milan, Italy
[2] Mario Negri Inst Pharmacol Res, I-20156 Milan, Italy
[3] Uppsala Univ, Dept Immunol Genet & Pathol, S-75185 Uppsala, Sweden
来源
关键词
CEREBRAL CAVERNOUS MALFORMATIONS; BLOOD-BRAIN-BARRIER; PERMEABILITY IN-VIVO; CELL-CELL JUNCTIONS; FLUID SHEAR-STRESS; PHOSPHATASE VE-PTP; LEUKOCYTE EXTRAVASATION; CCM PATHOGENESIS; TRANSENDOTHELIAL MIGRATION; MECHANOSENSORY COMPLEX;
D O I
10.1101/cshperspect.a029322
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endothelial cell - cell adherens junctions (AJs) supervise fundamental vascular functions, such as the control of permeability and transmigration of circulating leukocytes, and the maintenance of existing vessels and formation of new ones. These processes are often dysregulated in pathologies. However, the evidence that links dysfunction of endothelial AJs to human pathologies is mostly correlative. In this review, we present an update of the molecular organization of AJ complexes in endothelial cells (ECs) that is mainly based on observations from experimental models. Furthermore, we report in detail on a human pathology, cerebral cavernous malformation (CCM), which is initiated by loss-of-function mutations in the genes that encode the three cytoplasmic components of AJs (CCM1, CCM2, and CCM3). At present, these represent a unique example of mutations in components of endothelial AJs that cause human disease. We describe also how studies into the defects of AJs in CCM are shedding light on the crucial regulatory mechanisms and signaling activities of these endothelial structures. Although these observations are specific for CCM, they support the concept that dysfunction of endothelial AJs can directly contribute to human pathologies.
引用
收藏
页数:17
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