VEGF signaling inside vascular endothelial cells and beyond

被引:239
作者
Eichmann, Anne [1 ,2 ]
Simons, Michael [1 ,3 ]
机构
[1] Yale Univ, Sch Med, Dept Internal Med, Yale Cardiovasc Res Ctr,Sect Cardiovasc Med, New Haven, CT 06510 USA
[2] Coll France, Ctr Interdisciplinary Res Biol CIRB, F-75231 Paris, France
[3] Yale Univ, Sch Med, Dept Cell Biol, New Haven, CT 06510 USA
关键词
BRANCHING MORPHOGENESIS; MOLECULAR-MECHANISMS; BLOOD-VESSELS; ANGIOGENESIS; GROWTH; TIP; TRAFFICKING; PATHWAY; TRANSDUCTION; RECEPTORS;
D O I
10.1016/j.ceb.2012.02.002
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Vascular endothelial growth factor-A (VEGF-A) has long been recognized as the key regulator of vascular development and function in health and disease. VEGF is a secreted polypeptide that binds to transmembrane tyrosine kinase VEGF receptors on the plasma membrane, inducing their dimerization, activation and assembly of a membrane-proximal signaling complex. Recent studies have revealed that many key events of VEGFR signaling occur inside the endothelial cell and are regulated by endosomal receptor trafficking. Plasma membrane VEGFR interacting molecules, including vascular guidance receptors Neuropilins and Ephrins also regulate VEGFR endocytosis and trafficking. VEGF signaling is increasingly recognized for its roles outside of the vascular system, notably during neural development, and blood vessels regulate epithelial branching morphogenesis. We review here recent advances in our understanding of VEGF signaling and its biological roles.
引用
收藏
页码:188 / 193
页数:6
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