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白细胞介素-6是肿瘤坏死因子α诱导的3T3-L1脂肪细胞中脂肪相关蛋白的正向调节因子。

Interleukin-6 is a positive regulator of tumor necrosis factor alpha-induced adipose-related protein in 3T3-L1 adipocytes.

作者信息

Fasshauer Mathias, Kralisch Susan, Klier Margit, Lossner Ulrike, Bluher Matthias, Chambaut-Guérin Anne-Marie, Klein Johannes, Paschke Ralf

机构信息

University of Leipzig, Department of Internal Medicine III, 04103 Leipzig, Germany.

出版信息

FEBS Lett. 2004 Feb 27;560(1-3):153-7. doi: 10.1016/S0014-5793(04)00096-1.

Abstract

Tumor necrosis factor (TNF) alpha-induced adipose-related protein (TIARP) is a novel TNFalpha-stimulated protein in adipocytes. Besides TNFalpha, interleukin (IL)-6 has recently been shown to be another adipocytokine implicated in insulin resistance. Therefore, the impact of IL-6 on TIARP gene expression in 3T3-L1 adipocytes was determined by quantitative real-time reverse transcription-polymerase chain reaction. Interestingly, TIARP mRNA expression was stimulated up to 3.8-fold by IL-6 in a dose-dependent fashion with significant stimulation detectable at effector concentrations as low as 3 ng/ml and maximal effects seen at 100 ng/ml IL-6. Induction of TIARP mRNA by IL-6 was time-dependent with significant upregulation occurring as early as 2 h after effector addition and maximal effects observed at 4 h. In parallel, TIARP protein synthesis was upregulated with maximal effects seen after 8 h of IL-6 treatment. Furthermore, the Janus kinase 2 inhibitor AG490 decreased TIARP mRNA expression. The increase of TIARP mRNA could be reversed by withdrawal of IL-6 for 24 h. Furthermore, TIARP mRNA induction by IL-6 was also seen in brown adipocytes but not in muscle and liver cells. Taken together, these results show that TIARP is acutely regulated in adipose tissue not only by TNFalpha but also by IL-6 which has been shown to be another important cytokine implicated in the pathogenesis of insulin resistance.

摘要

肿瘤坏死因子(TNF)α诱导的脂肪相关蛋白(TIARP)是脂肪细胞中一种新的TNFα刺激蛋白。除了TNFα,白细胞介素(IL)-6最近被证明是另一种与胰岛素抵抗有关的脂肪细胞因子。因此,通过定量实时逆转录-聚合酶链反应测定了IL-6对3T3-L1脂肪细胞中TIARP基因表达的影响。有趣的是,IL-6以剂量依赖的方式刺激TIARP mRNA表达高达3.8倍,在低至3 ng/ml的效应浓度下即可检测到显著刺激,在100 ng/ml IL-6时达到最大效应。IL-6对TIARP mRNA的诱导是时间依赖性的,早在加入效应物后2小时就出现显著上调,在4小时时观察到最大效应。同时,TIARP蛋白合成上调,在IL-6处理8小时后达到最大效应。此外,Janus激酶2抑制剂AG490降低了TIARP mRNA表达。去除IL-6 24小时后,TIARP mRNA的增加可被逆转。此外,IL-6对TIARP mRNA的诱导在棕色脂肪细胞中也可见,但在肌肉和肝细胞中未见。综上所述,这些结果表明,TIARP在脂肪组织中不仅受到TNFα的急性调节,还受到IL-6的急性调节,IL-6已被证明是胰岛素抵抗发病机制中另一种重要的细胞因子。

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