Zaid Hilal, Antonescu Costin N, Randhawa Varinder K, Klip Amira
Program in Cell Biology, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
Biochem J. 2008 Jul 15;413(2):201-15. doi: 10.1042/BJ20080723.
Glucose entry into muscle cells is precisely regulated by insulin, through recruitment of GLUT4 (glucose transporter-4) to the membrane of muscle and fat cells. Work done over more than two decades has contributed to mapping the insulin signalling and GLUT4 vesicle trafficking events underpinning this response. In spite of this intensive scientific research, there are outstanding questions that continue to challenge us today. The present review summarizes the knowledge in the field, with emphasis on the latest breakthroughs in insulin signalling at the level of AS160 (Akt substrate of 160 kDa), TBC1D1 (tre-2/USP6, BUB2, cdc16 domain family member 1) and their target Rab proteins; in vesicle trafficking at the level of vesicle mobilization, tethering, docking and fusion with the membrane; and in the participation of the cytoskeleton to achieve optimal temporal and spatial location of insulin-derived signals and GLUT4 vesicles.
胰岛素通过将GLUT4(葡萄糖转运蛋白4)募集到肌肉和脂肪细胞的膜上,精确地调节葡萄糖进入肌肉细胞的过程。二十多年来的研究工作有助于描绘出支撑这一反应的胰岛素信号传导和GLUT4囊泡运输事件。尽管进行了深入的科学研究,但仍有一些悬而未决的问题在今天继续挑战着我们。本综述总结了该领域的知识,重点介绍了在AS160(160 kDa的Akt底物)、TBC1D1(tre-2/USP6、BUB2、cdc16结构域家族成员1)及其靶标Rab蛋白水平上胰岛素信号传导的最新突破;在囊泡运输方面,包括囊泡动员、拴系、对接以及与膜融合的水平;以及细胞骨架在实现胰岛素衍生信号和GLUT4囊泡的最佳时空定位中的参与情况。