Chiang Shian-Huey, Chang Louise, Saltiel Alan R
Life Sciences Institute, University of Michigan, Ann Arbor, USA.
Methods Enzymol. 2006;406:701-14. doi: 10.1016/S0076-6879(06)06055-1.
Insulin stimulates glucose uptake in insulin-responsive tissues by means of the translocation of the glucose transporter GLUT4 from intracellular sites to the plasma membrane. Two pathways are required, one involving activation of a phosphatidylinositol 3-kinase (PI 3-kinase) and downstream protein kinases, and one involving activation of the Rho-family GTPase TC10. TC10 activation by insulin is catalyzed by the exchange factor C3G, which is translocated to lipid rafts along with its binding partner CrkII as a consequence of Cbl tyrosine phosphorylation by the insulin receptor. This activation of TC10 is dependent on localization of TC10 in the lipid raft subdomains of the plasma membrane. We describe experimental approaches using the insulin-responsive cell line 3T3-L1 adipocytes to study the role of TC10 in insulin-stimulated glucose transport.
胰岛素通过葡萄糖转运蛋白GLUT4从细胞内位点转位至质膜,从而刺激胰岛素反应性组织摄取葡萄糖。这需要两条途径,一条涉及磷脂酰肌醇3激酶(PI 3激酶)及下游蛋白激酶的激活,另一条涉及Rho家族GTP酶TC10的激活。胰岛素对TC10的激活由交换因子C3G催化,由于胰岛素受体使Cbl酪氨酸磷酸化,C3G与其结合伴侣CrkII一起转位至脂筏。TC10的这种激活依赖于TC10在质膜脂筏亚结构域中的定位。我们描述了使用胰岛素反应性细胞系3T3-L1脂肪细胞的实验方法,以研究TC10在胰岛素刺激的葡萄糖转运中的作用。