Src-Mediated Phosphorylation of Dynamin and Cortactin Regulates the "Constitutive" Endocytosis of Transferrin

被引:86
作者
Cao, Hong
Chen, Jing
Krueger, Eugene W.
McNiven, Mark A. [1 ]
机构
[1] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
PROTEIN-TYROSINE KINASES; GROWTH-FACTOR; V-SRC; RECEPTOR INTERNALIZATION; VESICLE FORMATION; K562; CELLS; CLATHRIN; COMPLEX; MEMBRANE; BINDING;
D O I
10.1128/MCB.00330-09
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 mechanisms by which epithelial cells regulate clathrin-mediated endocytosis (CME) of transferrin are poorly defined and generally viewed as a constitutive process that occurs continuously without regulatory constraints. In this study, we demonstrate for the first time that endocytosis of the transferrin receptor is a regulated process that requires activated Src kinase and, subsequently, phosphorylation of two important components of the endocytic machinery, namely, the large GTPase dynamin 2 (Dyn2) and its associated actin-binding protein, cortactin (Cort). To our knowledge these findings are among the first to implicate an Src-mediated endocytic cascade in what was previously presumed to be a nonregulated internalization process.
引用
收藏
页码:781 / 792
页数:12
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