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金橘素通过调节肝细胞核因子 LXRα 激活抑制血管生成素样蛋白 3(ANGPTL3)基因表达的调脂作用。

The Lipid-Modulating Effect of Tangeretin on the Inhibition of Angiopoietin-like 3 (ANGPTL3) Gene Expression through Regulation of LXRα Activation in Hepatic Cells.

机构信息

Center of Medical Genetics, Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation, Hualien 97004, Taiwan.

Department of Molecular Biology and Human Genetics, Tzu Chi University, Hualien 97004, Taiwan.

出版信息

Int J Mol Sci. 2021 Sep 12;22(18):9853. doi: 10.3390/ijms22189853.

Abstract

The excessive accumulation of TG-rich lipoproteins (TGRLs) in plasma is associated with dyslipidemia and atherosclerotic cardiovascular diseases (ASCVDs). Tangeretin is a bioactive pentamethoxyflavone mainly found in citrus peels, and it has been reported to protect against hyperlipidemia, diabetes, and obesity. The aim of this study was to investigate the lipid-modulating effects and the underlying mechanisms of tangeretin action in hepatic cells. Transcriptome and bioinformatics analyses with the Gene Ontology (GO) database showed that tangeretin significantly regulated a set of 13 differentially expressed genes (DEGs) associated with the regulation of lipoprotein lipase (LPL) activity. Among these DEGs, angiopoietin-like 3 (ANGPTL3), an essential inhibitor of LPL catalytic activity that regulates TGRL metabolism in plasma, was markedly downregulated by tangeretin. We demonstrated that tangeretin significantly inhibited the mRNA expression of ANGPTL3 in HepG2 and Huh-7 cells. Tangeretin treatment of hepatic cells also reduced the levels of both intracellular and secreted ANGPTL3 proteins. Moreover, we found that inhibition of ANGPTL3 production by tangeretin augmented LPL activity. We further demonstrated that the transcriptional activity of the ANGPTL3 promoter was significantly attenuated by tangeretin, and we identified a DNA element located between the -250 and -121 positions that responded to tangeretin. Furthermore, we found that tangeretin did not alter the levels of the nuclear liver X receptor α (LXRα) protein, an essential transcription factor that binds to the tangeretin-responsive element, but it can counteract LXRα-mediated ANGPTL3 transcription. On the basis of molecular docking analysis, tangeretin was predicted to bind to the ligand-binding domain of LXRα, which would result in suppression of LXRα activation. Our findings support the hypothesis that tangeretin exerts a lipid-lowering effect by modulating the LXRα-ANGPTL3-LPL pathway, and thus, it can be used as a potential phytochemical for the prevention or treatment of dyslipidemia.

摘要

血浆中甘油三酯(TG)丰富脂蛋白(TGRL)的过度积累与血脂异常和动脉粥样硬化性心血管疾病(ASCVD)有关。桔皮素是一种主要存在于桔皮中的生物活性五甲氧基黄酮,已被报道可预防高脂血症、糖尿病和肥胖症。本研究旨在研究桔皮素在肝细胞中的调脂作用及其作用机制。通过基因本体(GO)数据库进行转录组和生物信息学分析表明,桔皮素显著调节了一组与脂蛋白脂肪酶(LPL)活性调节相关的 13 个差异表达基因(DEG)。在这些 DEG 中,血管生成素样 3(ANGPTL3)是 LPL 催化活性的必需抑制剂,可调节血浆中的 TGRL 代谢,其表达明显被桔皮素下调。我们证明桔皮素显著抑制 HepG2 和 Huh-7 细胞中 ANGPTL3 的 mRNA 表达。桔皮素处理肝细胞还降低了细胞内和分泌的 ANGPTL3 蛋白水平。此外,我们发现桔皮素抑制 ANGPTL3 的产生可增强 LPL 活性。我们进一步证明,桔皮素显著减弱了 ANGPTL3 启动子的转录活性,并且我们鉴定了位于-250 到-121 位置之间的一个 DNA 元件,该元件对桔皮素反应。此外,我们发现桔皮素不会改变核肝 X 受体α(LXRα)蛋白的水平,LXRα 是一种必需的转录因子,可与桔皮素反应元件结合,但它可以拮抗 LXRα 介导的 ANGPTL3 转录。基于分子对接分析,桔皮素被预测与 LXRα 的配体结合域结合,从而抑制 LXRα 的激活。我们的研究结果支持桔皮素通过调节 LXRα-ANGPTL3-LPL 通路发挥降脂作用的假说,因此它可用作预防或治疗血脂异常的潜在植物化学物质。

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