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地塞米松通过不同的信号通路刺激L6骨骼肌细胞中GLUT1和GLUT4蛋白的表达。

Dexamethasone stimulates the expression of GLUT1 and GLUT4 proteins via different signalling pathways in L6 skeletal muscle cells.

作者信息

Ewart H S, Somwar R, Klip A

机构信息

Division of Cell Biology, The Hospital for Sick Children, Toronto, Ont., Canada.

出版信息

FEBS Lett. 1998 Jan 9;421(2):120-4. doi: 10.1016/s0014-5793(97)01549-4.

Abstract

It was recently demonstrated that dexamethasone treatment of L6 skeletal muscle cells resulted in an elevation of GLUT1 protein. However, the level of GLUT4 protein under these conditions was not examined. In addition, the signalling mechanism(s) leading to dexamethasone-induced expression of GLUT1 protein was not investigated. In the present study we investigated the effect of dexamethasone on the expression of GLUT1 and GLUT4 proteins in differentiated L6 muscle cells and the signalling mechanism(s) via which dexamethasone may act. Dexamethasone (300 nM) treatment for 24 h elevated GLUT1 and GLUT4 proteins by 68% and 94%, respectively, above control levels. These increases were due to de novo synthesis as shown by metabolic labelling with [35S]methionine. Incubation of cells with 100 nM wortmannin or 30 ng/ml rapamycin prevented the dexamethasone-stimulated elevation of GLUT1 protein. In contrast, neither of these inhibitors affected the elevation of GLUT4 protein by dexamethasone. Furthermore, dexamethasone down-regulated insulin receptor substrate-1 protein content by 42% and insulin-induced tyrosine phosphorylation of insulin receptor substrate-1 by 28%. The p70 ribosomal S6 kinase was not activated by dexamethasone and instead, dexamethasone attenuated the stimulation of this enzyme activity by insulin. These results suggest that dexamethasone induces the expression of GLUT1 and GLUT4 protein by independent signalling mechanisms with a concomitant depression of intracellular signalling by insulin.

摘要

最近有研究表明,地塞米松处理L6骨骼肌细胞会导致GLUT1蛋白水平升高。然而,在这些条件下GLUT4蛋白的水平并未被检测。此外,导致地塞米松诱导GLUT1蛋白表达的信号机制也未被研究。在本研究中,我们调查了地塞米松对分化的L6肌肉细胞中GLUT1和GLUT4蛋白表达的影响,以及地塞米松可能发挥作用的信号机制。用300 nM地塞米松处理24小时后,GLUT1和GLUT4蛋白水平分别比对照水平升高了68%和94%。这些增加是由于从头合成,如用[35S]甲硫氨酸进行代谢标记所示。用100 nM渥曼青霉素或30 ng/ml雷帕霉素处理细胞可阻止地塞米松刺激的GLUT1蛋白升高。相比之下,这些抑制剂均未影响地塞米松对GLUT4蛋白的升高作用。此外,地塞米松使胰岛素受体底物-1蛋白含量下调了42%,并使胰岛素诱导的胰岛素受体底物-1酪氨酸磷酸化降低了28%。地塞米松未激活p70核糖体S6激酶,相反,地塞米松减弱了胰岛素对该酶活性的刺激。这些结果表明,地塞米松通过独立的信号机制诱导GLUT1和GLUT4蛋白的表达,同时抑制胰岛素的细胞内信号传导。

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