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分析(-)-表没食子儿茶素没食子酸酯诱导胰岛素诱导转录因子 SHARP-2 基因的机制。

Analysis of induction mechanisms of an insulin-inducible transcription factor SHARP-2 gene by (-)-epigallocatechin-3-gallate.

机构信息

Department of Health and Nutritional Science, Faculty of Human Health Science, Matsumoto University , 2095-1 Niimura, Matsumoto, Nagano 390-1295, Japan.

出版信息

J Agric Food Chem. 2012 Oct 3;60(39):9850-5. doi: 10.1021/jf302607j. Epub 2012 Sep 21.

Abstract

The rat enhancer of split- and hairy-related protein-2 (SHARP-2) is an insulin-inducible transcription factor. In this study, we examined the mechanism(s) involved in the regulation of the rat SHARP-2 gene expression by (-)-epigallocatechin-3-gallate (EGCG). The induction of SHARP-2 mRNA by EGCG was repressed by pretreatments with inhibitors for either phosphoinositide 3-kinase (PI3K) or RNA polymerase II. Then, we examined a biological relationship between EGCG and transcription factor NF-κB interfering with the insulin action. The protein levels of the NF-κB were rapidly decreased by an EGCG treatment. Finally, the mechanism(s) of transcriptional activation of the rat SHARP-2 gene by both NF-κB and EGCG was analyzed. While overexpression of the NF-κB p65 protein decreased the promoter activity of the SHARP-2 gene, EGCG did not affect it. Thus, we conclude that EGCG induces the expression of the rat SHARP-2 gene via both the PI3K pathway and degradation of the NF-κB p65 protein.

摘要

大鼠分裂增强子结合蛋白 2(SHARP-2)是一种胰岛素诱导的转录因子。在这项研究中,我们研究了(-)-表没食子儿茶素没食子酸酯(EGCG)调控大鼠 SHARP-2 基因表达的机制。用磷酸肌醇 3-激酶(PI3K)或 RNA 聚合酶 II 的抑制剂预处理会抑制 EGCG 诱导的 SHARP-2 mRNA 的产生。然后,我们研究了 EGCG 与干扰胰岛素作用的转录因子 NF-κB 之间的生物学关系。EGCG 处理可迅速降低 NF-κB 蛋白水平。最后,分析了 NF-κB 和 EGCG 对大鼠 SHARP-2 基因转录激活的机制。虽然 NF-κB p65 蛋白的过表达会降低 SHARP-2 基因的启动子活性,但 EGCG 对此没有影响。因此,我们得出结论,EGCG 通过 PI3K 途径和 NF-κB p65 蛋白的降解诱导大鼠 SHARP-2 基因的表达。

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