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Insulin-like growth factor I and insulin induce adipogenic-related gene expression in fetal brown adipocyte primary cultures.

机译:胰岛素样生长因子I和胰岛素诱导胎儿棕色脂肪细胞原代培养物中的脂肪形成相关基因表达。

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摘要

Fetal rat brown adipocytes show high-affinity binding sites for both insulin-like growth factor I (IGF-I) and insulin. Cell culture for 24 h in the presence of IGF-I or insulin, independently, up-regulated the mRNA expression of adipogenic-related genes, such as fatty acid synthase (FAS), glycerol-3-phosphate de-hydrogenase and insulin-regulated glucose transporter Glut4, and down-regulated the expression of phosphoenolpyruvate carboxykinase mRNA in a dose-dependent manner. Moreover, both IGF-I and insulin increased the FAS gene transcription rate at 2 h, producing a time-dependent accumulation of FAS mRNA. Furthermore IGF-I or insulin increased glucose uptake and lipid content throughout the 24 h culture period. Our results suggest that both IGF-I and insulin are major signals involved in initiating and/or maintaining the expression of adipogenic-related genes in fetal rat brown adipocytes.
机译:胎儿大鼠棕色脂肪细胞对胰岛素样生长因子I(IGF-1)和胰岛素均显示高亲和力结合位点。在IGF-I或胰岛素存在下,细胞培养24小时独立地上调了脂肪合成相关基因的mRNA表达,例如脂肪酸合酶(FAS),3-磷酸甘油三磷酸脱氢酶和胰岛素调节葡萄糖转运蛋白Glut4,并以剂量​​依赖性方式下调磷酸烯醇丙酮酸羧化激酶mRNA的表达。此外,IGF-I和胰岛素都在2 h时增加了FAS基因的转录速度,从而产生了时间依赖性的FAS mRNA积累。此外,在整个24小时的培养过程中,IGF-1或胰岛素均可增加葡萄糖摄取和脂质含量。我们的结果表明,IGF-I和胰岛素都是在胎鼠棕色脂肪细胞中引发和/或维持脂肪形成相关基因表达的主要信号。

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