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首页> 外文期刊>Molecular and Cellular Endocrinology >Plasminogen activator inhibitor-1 expression and secretion are stimulated by growth hormone and interleukin-6 in 3T3-L1 adipocytes.
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Plasminogen activator inhibitor-1 expression and secretion are stimulated by growth hormone and interleukin-6 in 3T3-L1 adipocytes.

机译:在3T3-L1脂肪细胞中,生长激素和白介素6刺激纤溶酶原激活物抑制剂1的表达和分泌。

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Various adipocytokines have been described which influence insulin sensitivity and vascular function profoundly and might, therefore, potentially link obesity, insulin resistance, and atherosclerosis. Among those, plasminogen activator inhibitor (PAI)-1 is an adipose-secreted factor upregulated in obesity and insulin resistance that inhibits fibrinolysis. Furthermore, recent studies in knockout mice suggest that PAI-1 directly impairs insulin sensitivity. In the current study, the impact of growth hormone (GH) and interleukin (IL)-6 on PAI-1 mRNA synthesis and secretion was determined in 3T3-L1 adipocytes. Interestingly, 500 ng/ml GH and 30 ng/ml IL-6 increased PAI-1 secretion five-fold and 3.6-fold, respectively. Furthermore, GH and IL-6 induced PAI-1 mRNA by up to 7.3-fold, and 3.6-fold, respectively, in a time-dependent fashion with significant stimulation seen at concentrations as low as 5 ng/ml GH and 10 ng/ml IL-6. Other insulin resistance-inducing hormones which stimulated PAI-1 synthesis included insulin, TNFalpha, and dexamethasone. Studies using pharmacological inhibitors suggested that basal and GH-induced PAI-1 synthesis were at least in part mediated by p44/42 mitogen-activated protein kinase but not janus kinase 2 and phosphatidylinositol 3-kinase. Taken together, our results show a differential regulation of PAI-1 mRNA by insulin resistance-inducing hormones including GH and IL-6.
机译:已经描述了各种脂肪细胞因子,它们深刻影响胰岛素敏感性和血管功能,因此可能潜在地与肥胖症​​,胰岛素抵抗和动脉粥样硬化有关。其中,纤溶酶原激活物抑制剂(PAI)-1是肥胖和胰岛素抵抗中上调的脂肪分泌因子,可抑制纤维蛋白溶解。此外,最近在基因敲除小鼠中的研究表明,PAI-1直接损害胰岛素敏感性。在当前的研究中,确定了3T3-L1脂肪细胞中生长激素(GH)和白介素(IL)-6对PAI-1 mRNA合成和分泌的影响。有趣的是,500 ng / ml GH和30 ng / ml IL-6分别使PAI-1分泌增加了5倍和3.6倍。此外,GH和IL-6以时间依赖性方式分别诱导PAI-1 mRNA分别高达7.3倍和3.6倍,并且在浓度低至5 ng / ml GH和10 ng / ml时均能产生明显的刺激作用。 ml IL-6。刺激PAI-1合成的其他诱导胰岛素抵抗的激素包括胰岛素,TNFα和地塞米松。使用药理学抑制剂的研究表明,基础和GH诱导的PAI-1合成至少部分由p44 / 42丝裂原激活的蛋白激酶介导,而不是由janus激酶2和磷脂酰肌醇3激酶介导。两者合计,我们的结果表明,胰岛素抵抗诱导激素包括GH和IL-6对PAI-1 mRNA的差异调节。

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