VEGF receptor trafficking in angiogenesis

被引:32
|
作者
Scott, Alice [1 ]
Mellor, Harry [1 ]
机构
[1] Univ Bristol, Sch Med Sci, Dept Biochem, Bristol BS8 1TD, Avon, England
关键词
angiogenesis; endocytosis; intracellular trafficking; vascular endothelial growth factor (VEGF); ENDOTHELIAL-CELLS; DOWN-REGULATION; KINASE-ACTIVITY; DEGRADATION; ENDOCYTOSIS; KDR; INTERNALIZATION; UBIQUITINATION; LOCALIZATION; CAVEOLIN-1;
D O I
10.1042/BST0371184
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The intracellular trafficking of receptors provides a way to control the overall sensitivity of a cell to receptor stimulation. These sorting pathways are also used to shape the balance of signals that are generated in response to receptor activation. The major pro-angiogenic growth factor receptor is VEGFR2 (vascular endothelial growth factor 2). VEGFR2 activates a very similar set of signalling pathways to other RTKs (receptor tyrosine kinases); however, its intracellular trafficking is very different. Furthermore, VEGFR2 can form a complex with a range of different angiogenic regulators that in turn regulate the trafficking of VEGFR2 through the endosomal pathway. This regulated trafficking of VEGFR2 has important consequences for angiogenic signalling and is a clear demonstration of how the endosomal pathway plays a critical role in connecting receptor signalling pathways to cellular events.
引用
收藏
页码:1184 / 1188
页数:5
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