Moreno-Aliaga M J, Stanhope K L, Havel P J
Department of Physiology and Nutrition, University of Navarra, Pamplona, 31008, Spain.
Biochem Biophys Res Commun. 2001 May 11;283(3):544-8. doi: 10.1006/bbrc.2001.4822.
Insulin-stimulated glucose metabolism plays a key role in the regulation of leptin mRNA expression and protein secretion. However, it is not known whether stimulation of leptin production by glucose metabolism is regulated at the level of promoter activation or at a step distal to the promoter. Therefore, in order to investigate the transcriptional regulation of the leptin promoter by insulin-stimulated glucose metabolism, 3T3-L1 cells were transfected with a plasmid containing the leptin promoter driving a luciferase reporter gene. Leptin promoter activity was increased after 48 hours of treatment by 219 +/- 64 (p = 0.028) and 225 +/- 69% (p = 0.046) at insulin concentrations of 16 and 160 nM, respectively. The activation of the leptin promoter induced by insulin (16 nM) was markedly inhibited by 2-deoxy-D-glucose (2-DG, 50 mg/dl), a competitive inhibitor of glucose metabolism. The increment of insulin-stimulated leptin promoter activation was reduced by 52 +/- 11% (p = 0.028 vs insulin alone). The activity of a control plasmid (pGL2-Control) was unaffected by insulin or 2-DG. These results provide strong evidence that insulin-stimulated glucose metabolism, and not insulin per se, mediates the effects of insulin to increase the transcriptional activity of the leptin promoter.
胰岛素刺激的葡萄糖代谢在瘦素mRNA表达和蛋白质分泌的调节中起关键作用。然而,葡萄糖代谢对瘦素产生的刺激是否在启动子激活水平或启动子远端的步骤受到调节尚不清楚。因此,为了研究胰岛素刺激的葡萄糖代谢对瘦素启动子的转录调控,用含有驱动荧光素酶报告基因的瘦素启动子的质粒转染3T3-L1细胞。在胰岛素浓度分别为16和160 nM处理48小时后瘦素启动子活性分别增加了219±64(p = 0.028)和225±69%(p = 0.046)。胰岛素(16 nM)诱导的瘦素启动子激活被葡萄糖代谢的竞争性抑制剂2-脱氧-D-葡萄糖(2-DG,50 mg/dl)显著抑制。胰岛素刺激的瘦素启动子激活的增量降低了52±11%(与单独使用胰岛素相比,p = 0.028)。对照质粒(pGL2-Control)的活性不受胰岛素或2-DG的影响。这些结果提供了强有力的证据,表明胰岛素刺激的葡萄糖代谢而非胰岛素本身介导了胰岛素增加瘦素启动子转录活性的作用。