Department of Pharmacology, Oita University Faculty of Medicine, Hasama, Yufu, Oita, Japan.
Mol Cell Biol. 2013 Dec;33(24):4834-43. doi: 10.1128/MCB.00895-13. Epub 2013 Oct 7.
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 site.
募集特定分子到特定膜位点对于专门的膜细胞器之间的通讯是至关重要的。在本研究中,我们鉴定了 IQGAP1 作为一种新型的 GDP 结合 Rab27a 相互作用蛋白。我们发现,IQGAP1 与 GDP 结合的 Rab27a 相互作用,当它与 GTP 结合的 Cdc42 形成复合物时。我们还发现 IQGAP1 调节胰岛素分泌膜的内吞作用。IQGAP1 的沉默抑制了内吞作用和葡萄糖诱导的内吞机制的重新分布,包括 Rab27a 及其结合蛋白 coronin 3。这些过程也可以通过破坏与显性负性 IQGAP1 和 Cdc42 的三聚复合物来抑制。这些结果表明,胰岛素分泌激动剂葡萄糖激活 Cdc42 募集内吞机制到 IQGAP1 在细胞外周,并调节该膜位点的内吞作用。