Teruel T, Valverde A M, Benito M, Lorenzo M
Departamento de Bioquímica y Biología Molecular II, Facultad de Farmacia, Universidad Complutense, Madrid, Spain.
Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):627-32. doi: 10.1042/bj3190627.
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.
胎鼠棕色脂肪细胞对胰岛素样生长因子I(IGF-I)和胰岛素均显示出高亲和力结合位点。在IGF-I或胰岛素单独存在的情况下进行24小时细胞培养,可上调脂肪生成相关基因的mRNA表达,如脂肪酸合酶(FAS)、甘油-3-磷酸脱氢酶和胰岛素调节的葡萄糖转运蛋白Glut4,并以剂量依赖方式下调磷酸烯醇丙酮酸羧激酶mRNA的表达。此外,IGF-I和胰岛素在2小时时均增加了FAS基因转录率,导致FAS mRNA呈时间依赖性积累。此外,在整个24小时培养期内,IGF-I或胰岛素均增加了葡萄糖摄取和脂质含量。我们的结果表明,IGF-I和胰岛素都是参与启动和/或维持胎鼠棕色脂肪细胞中脂肪生成相关基因表达的主要信号。