Gypakis A, Wasner H K
Deutsches Diabetes-Forschungsinstitut, Abteilung für klinische Biochemie, Düsseldorf, Germany.
Biol Chem. 2000 Nov;381(11):1139-41. doi: 10.1515/BC.2000.140.
It has been suggested that downstream signaling from the insulin receptor to the level of the protein kinases and protein phosphatases is accomplished by prosta-glandylinositol cyclic phosphate (cyclic PIP), a proposed second messenger of insulin. However, evidence points also to both phosphatidylinositol 3-kinase, which binds to the tyrosine phosphorylated insulin receptor substrate-1, and the Ras complex in insulin's downstream signaling. We have examined whether a correlation exists between these various observations. It was found that wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase, prevented insulin-induced, as well as cyclic PIP-induced activation of glucose transport, indicating that PI 3-kinase action on glucose transport involves downstream signaling of both insulin and cyclic PIP. Wortmannin has no effect on cyclic PIP synthase activity nor on the substrate production for cyclic PIP synthesis either, indicating that the functional role of PI 3-kinase is exclusively downstream of cyclic PIP.
有人提出,从胰岛素受体到蛋白激酶和蛋白磷酸酶水平的下游信号传导是由前列腺素肌醇环磷酸酯(环PIP)完成的,环PIP是一种推测的胰岛素第二信使。然而,证据也指向磷脂酰肌醇3激酶(它与酪氨酸磷酸化的胰岛素受体底物-1结合)以及胰岛素下游信号传导中的Ras复合物。我们研究了这些不同观察结果之间是否存在相关性。结果发现,磷脂酰肌醇3激酶的特异性抑制剂渥曼青霉素可阻止胰岛素诱导的以及环PIP诱导的葡萄糖转运激活,这表明PI 3激酶对葡萄糖转运的作用涉及胰岛素和环PIP的下游信号传导。渥曼青霉素对环PIP合酶活性以及环PIP合成的底物产生均无影响,这表明PI 3激酶的功能作用仅在环PIP的下游。