Jiang Zhen Y, Zhou Qiong L, Coleman Kerri A, Chouinard My, Boese Queta, Czech Michael P
Program in Molecular Medicine, University of Massachusetts Medical School, 373 Plantation Street, Worcester, MA 01605, USA.
Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7569-74. doi: 10.1073/pnas.1332633100. Epub 2003 Jun 13.
Glucose homeostasis is controlled by insulin in part through the translocation of intracellular glucose transporter 4 to the plasma membrane in muscle and fat cells. Akt/protein kinase B downstream of phosphatidylinositol 3-kinase has been implicated in this insulin-signaling pathway, but results with a variety of reagents including Akt1-/- and Akt2-/- mice have been equivocal. Here we report the application of small interfering RNA-directed gene silencing to deplete both Akt1 and Akt2 in cultured 3T3-L1 adipocytes. Loss of Akt1 alone slightly impaired insulin-mediated hexose transport activity but had no detectable effect on glycogen synthase kinase (GSK)-3 phosphorylation. In contrast, depletion of Akt2 alone by 70% inhibited approximately half of the insulin responsiveness. Combined depletions of Akt1 plus Akt2 in these cells even more markedly attenuated insulin action on glucose transporter 4 movements, hexose transport activity, and GSK-3 phosphorylation. These data demonstrate a primary role of Akt2 in insulin signaling, significant functional redundancy of Akt1 and Akt2 isoforms in this pathway, and an absolute requirement of Akt protein kinases for regulation of glucose transport and GSK-3 in cultured adipocytes.
葡萄糖稳态部分受胰岛素控制,通过细胞内葡萄糖转运蛋白4向肌肉和脂肪细胞质膜的转位来实现。磷脂酰肌醇3激酶下游的Akt/蛋白激酶B参与了这一胰岛素信号通路,但包括Akt1 - / - 和Akt2 - / - 小鼠在内的各种试剂的实验结果并不明确。在此,我们报告了应用小干扰RNA介导的基因沉默技术,在培养的3T3 - L1脂肪细胞中同时敲低Akt1和Akt2。单独敲低Akt1会轻微损害胰岛素介导的己糖转运活性,但对糖原合酶激酶(GSK)-3磷酸化没有可检测到的影响。相反,单独将Akt2敲低70%会抑制约一半的胰岛素反应性。在这些细胞中同时敲低Akt1和Akt2,更显著地减弱了胰岛素对葡萄糖转运蛋白4转位、己糖转运活性和GSK - 3磷酸化的作用。这些数据表明Akt2在胰岛素信号传导中起主要作用,Akt1和Akt2亚型在该通路中存在显著的功能冗余,并且在培养的脂肪细胞中,Akt蛋白激酶对于调节葡萄糖转运和GSK - 3是绝对必需的。