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胰岛素样生长因子I和胰岛素可诱导胎儿棕色脂肪细胞原代培养物中脂肪生成相关基因的表达。

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

作者信息

Teruel T, Valverde A M, Benito M, Lorenzo M

机构信息

Departamento de Bioquímica y Biología Molecular II, Facultad de Farmacia, Universidad Complutense, Madrid, Spain.

出版信息

Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):627-32. doi: 10.1042/bj3190627.

Abstract

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.

摘要

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。

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