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催乳素或生长激素通过STAT5A介导在脂肪细胞中诱导丙酮酸脱氢酶激酶4的表达。

The STAT5A-mediated induction of pyruvate dehydrogenase kinase 4 expression by prolactin or growth hormone in adipocytes.

作者信息

White Ursula A, Coulter Ann A, Miles Tiffany K, Stephens Jacqueline M

机构信息

Department of Biological Sciences, Louisiana State University, Baton Rouge, Louisiana 70803, USA.

出版信息

Diabetes. 2007 Jun;56(6):1623-9. doi: 10.2337/db06-1286. Epub 2007 Mar 14.

Abstract

The purpose of this study was to determine whether pyruvate dehydrogenase kinase (PDK)4 was expressed in adipocytes and whether PDK4 expression was hormonally regulated in fat cells. Both Northern blot and Western blot analyses were conducted on samples isolated from 3T3-L1 adipocytes after various treatments with prolactin (PRL), growth hormone (GH), and/or insulin. Transfection of PDK4 promoter reporter constructs was performed. In addition, glucose uptake measurements were conducted. Our studies demonstrate that PRL and porcine GH can induce the expression of PDK4 in 3T3-L1 adipocytes. Our studies also show that insulin pretreatment can attenuate the ability of these hormones to induce PDK4 mRNA expression. In addition, we identified a hormone-responsive region in the murine PDK4 promoter and characterized a STAT5 binding site in this region that mediates the PRL (sheep) and GH (porcine) induction in PDK4 expression in 3T3-L1 adipocytes. PDK4 is a STAT5A target gene. PRL is a potent inducer of PDK4 protein levels, results in an inhibition of insulin-stimulated glucose transport in fat cells, and likely contributes to PRL-induced insulin resistance.

摘要

本研究的目的是确定丙酮酸脱氢酶激酶(PDK)4是否在脂肪细胞中表达,以及PDK4的表达在脂肪细胞中是否受激素调节。在用催乳素(PRL)、生长激素(GH)和/或胰岛素进行各种处理后,对从3T3-L1脂肪细胞分离的样本进行了Northern印迹和Western印迹分析。进行了PDK4启动子报告基因构建体的转染。此外,还进行了葡萄糖摄取测量。我们的研究表明,PRL和猪GH可诱导3T3-L1脂肪细胞中PDK4的表达。我们的研究还表明,胰岛素预处理可减弱这些激素诱导PDK4 mRNA表达的能力。此外,我们在小鼠PDK4启动子中鉴定出一个激素反应区域,并在该区域表征了一个STAT5结合位点,该位点介导PRL(绵羊)和GH(猪)对3T3-L1脂肪细胞中PDK4表达的诱导作用。PDK4是STAT5A的靶基因。PRL是PDK4蛋白水平的有效诱导剂,导致脂肪细胞中胰岛素刺激的葡萄糖转运受到抑制,并可能导致PRL诱导的胰岛素抵抗。

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