Carel K, Kummer J L, Schubert C, Leitner W, Heidenreich K A, Draznin B
Medical Research Service, Veterans Affairs Medical Center, Denver, Colorado 80220, USA.
J Biol Chem. 1996 Nov 29;271(48):30625-30. doi: 10.1074/jbc.271.48.30625.
To characterize tissue-specific differences in insulin signaling, we compared the mechanisms of mitogen-activated protein (MAP) kinase activation by insulin in the mitogenically active 3T3-L1 fibroblasts with the metabolically active 3T3-L1 adipocytes. In both cell lines, insulin significantly increased p21(ras).GTP loading (1.5-2-fold) and MAP kinase activity (5-8-fold). Inhibition of Ras farnesylation with lovastatin blocked activation of p21(ras) and Raf-1 kinase in both 3T3-L1 fibroblasts and 3T3-L1 adipocytes. In 3T3-L1 fibroblasts, this was accompanied by an inhibition of the stimulatory effect of insulin on MAP kinase. In contrast, in 3T3-L1 adipocytes, despite an inhibition of activation of p21(ras) and Raf-1 by lovastatin, insulin continued to stimulate MAP kinase activity. Fractionation of the cell lysates on the FPLC Mono-Q column revealed that lovastatin inhibited insulin stimulation of ERK2 (and, to a lesser extent, ERK1) in 3T3-L1 fibroblasts and had no effect on the insulin-stimulated ERK2 in 3T3-L1 adipocytes. These results demonstrate an important distinction between the mechanism of insulin signaling in the metabolically and mitogenically active cells. Insulin activates MAP kinase by the Ras-dependent pathway in the 3T3-L1 fibroblasts and by the Ras-independent pathway in the 3T3-L1 adipocytes.
为了描述胰岛素信号传导中的组织特异性差异,我们比较了胰岛素在有丝分裂活性的3T3-L1成纤维细胞和代谢活性的3T3-L1脂肪细胞中激活丝裂原活化蛋白(MAP)激酶的机制。在这两种细胞系中,胰岛素均显著增加p21(ras).GTP负载(1.5至2倍)和MAP激酶活性(5至8倍)。用洛伐他汀抑制Ras法尼基化可阻断3T3-L1成纤维细胞和3T3-L1脂肪细胞中p21(ras)和Raf-1激酶的激活。在3T3-L1成纤维细胞中,这伴随着胰岛素对MAP激酶刺激作用的抑制。相反,在3T3-L1脂肪细胞中,尽管洛伐他汀抑制了p21(ras)和Raf-1的激活,但胰岛素仍继续刺激MAP激酶活性。在FPLC Mono-Q柱上对细胞裂解物进行分级分离显示,洛伐他汀抑制3T3-L1成纤维细胞中胰岛素对ERK2(以及程度较轻的ERK1)的刺激,而对3T3-L1脂肪细胞中胰岛素刺激的ERK2没有影响。这些结果表明了代谢活性和有丝分裂活性细胞中胰岛素信号传导机制的重要区别。胰岛素在3T3-L1成纤维细胞中通过Ras依赖性途径激活MAP激酶,而在3T3-L1脂肪细胞中通过Ras非依赖性途径激活MAP激酶。