Activated Cdc42-Bound IQGAP1 Determines the Cellular Endocytic Site

被引:24
|
作者
Kimura, Toshihide [1 ]
Yamaoka, Mami [1 ]
Taniguchi, Shigeki [1 ]
Okamoto, Mitsuhiro [1 ]
Takei, Masahiro [1 ]
Ando, Tomomi [1 ]
Iwamatsu, Akihiro [2 ]
Watanabe, Takashi [3 ]
Kaibuchi, Kozo [3 ,4 ]
Ishizaki, Toshimasa [1 ]
Niki, Ichiro [1 ]
机构
[1] Oita Univ, Fac Med, Dept Pharmacol, Oita 87011, Japan
[2] Prot Res Network Inc, Midori Ku, Yokohama, Kanagawa, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Cell Pharmacol, Showa Ku, Nagoya, Aichi 4648601, Japan
[4] JST, CREST, Kawaguchi, Saitama, Japan
关键词
GDP-DISSOCIATION INHIBITOR; INSULIN GRANULES; BINDING-PROTEIN; RAB PROTEINS; BETA-CELLS; MEMBRANE; CDC42; EFFECTOR; RAC1; EXOCYTOSIS;
D O I
10.1128/MCB.00895-13
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
Recruitment of specific molecules to a specific membrane site is essential for communication between specialized membranous organelles. In the present study, we identified IQGAP1 as a novel GDP-bound-Rab27a-interacting protein. We found that IQGAP1 interacts with GDP-bound Rab27a when it forms a complex with GTP-bound Cdc42. We also found that IQGAP1 regulates the endocytosis of insulin secretory membranes. Silencing of IQGAP1 inhibits both endocytosis and the glucose-induced redistribution of endocytic machinery, including Rab27a and its binding protein coronin 3. These processes can also be inhibited by disruption of the trimeric complex with dominant negative IQGAP1 and Cdc42. These results indicate that activation of Cdc42 in response to the insulin secretagogue glucose recruits endocytic machinery to IQGAP1 at the cell periphery and regulates endocytosis at this membrane
引用
收藏
页码:4834 / 4843
页数:10
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