Uehara T, Tokumitsu Y, Nomura Y
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan.
Biochem Biophys Res Commun. 1995 May 16;210(2):574-80. doi: 10.1006/bbrc.1995.1698.
Wortmannin, a specific inhibitor of phosphatidylinositol 3-kinase (PI 3-kinase), inhibited adipocyte differentiation of 3T3-L1 fibroblasts induced by insulin/dexamethasone/IBMX (hormones/IBMX). Insulin as a key factor in the process of the adipocyte differentiation activated PI 3-kinase, Ras protein, and mitogen-activated protein kinase (MAP kinase, ERK) in 3T3-L1 fibroblasts. Pretreatment with wortmannin almost completely suppressed all these activations. These findings suggest that the sequential activation of PI 3-kinase, Ras protein, and MAP kinase is involved in the insulin signaling pathway(s) during differentiation by hormones/IBMX and in consequence of the inhibition of PI 3-kinase by wortmannin, the activation of Ras protein and MAP kinase which acts downstream of PI 3-kinase is suppressed and results in the inhibition of adipocyte differentiation.
渥曼青霉素是磷脂酰肌醇3激酶(PI 3激酶)的一种特异性抑制剂,它能抑制胰岛素/地塞米松/异丁基甲基黄嘌呤(激素/异丁基甲基黄嘌呤)诱导的3T3-L1成纤维细胞的脂肪细胞分化。胰岛素作为脂肪细胞分化过程中的关键因子,可激活3T3-L1成纤维细胞中的PI 3激酶、Ras蛋白和丝裂原活化蛋白激酶(MAP激酶,ERK)。用渥曼青霉素预处理几乎完全抑制了所有这些激活作用。这些发现表明,PI 3激酶、Ras蛋白和MAP激酶的顺序激活参与了激素/异丁基甲基黄嘌呤诱导分化过程中的胰岛素信号通路,并且由于渥曼青霉素对PI 3激酶的抑制作用,位于PI 3激酶下游的Ras蛋白和MAP激酶的激活受到抑制,从而导致脂肪细胞分化受到抑制。