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胰岛素对葡萄糖转运蛋白GLUT4的激活作用。

Activation of the glucose transporter GLUT4 by insulin.

作者信息

Furtado L Michelle, Somwar Romel, Sweeney Gary, Niu Wenyan, Klip Amira

机构信息

Programme in Cell Biology, Hospital for Sick Children, University of Toronto, ON, Canada.

出版信息

Biochem Cell Biol. 2002;80(5):569-78. doi: 10.1139/o02-156.

Abstract

The transport of glucose into cells and tissues is a highly regulated process, mediated by a family of facilitative glucose transporters (GLUTs). Insulin-stimulated glucose uptake is primarily mediated by the transporter isoform GLUT4, which is predominantly expressed in mature skeletal muscle and fat tissues. Our recent work suggests that two separate pathways are initiated in response to insulin: (i) to recruit transporters to the cell surface from intracellular pools and (ii) to increase the intrinsic activity of the transporters. These pathways are differentially inhibited by wortmannin, demonstrating that the two pathways do not operate in series. Conversely, inhibitors of p38 mitogen-activated protein kinase (MAPK) imply that p38 MAPK is involved only in the regulation of the pathway leading to the insulin-stimulated activation of GLUT4. This review discusses the evidence for the divergence of GLUT4 translocation and activity and proposed mechanisms for the regulation of GLUT4.

摘要

葡萄糖进入细胞和组织的转运是一个受到高度调控的过程,由一组易化性葡萄糖转运蛋白(GLUTs)介导。胰岛素刺激的葡萄糖摄取主要由转运体亚型GLUT4介导,GLUT4主要在成熟骨骼肌和脂肪组织中表达。我们最近的研究表明,胰岛素引发了两条独立的途径:(i)将转运体从细胞内池招募到细胞表面;(ii)增加转运体的内在活性。渥曼青霉素对这两条途径有不同的抑制作用,表明这两条途径并非串联运行。相反,p38丝裂原活化蛋白激酶(MAPK)抑制剂表明p38 MAPK仅参与导致胰岛素刺激的GLUT4活化途径的调控。本综述讨论了GLUT4转位和活性分歧的证据以及GLUT4调控的潜在机制。

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