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槲皮素通过抑制C/EBPβ的转录活性来抑制载脂蛋白B的表达。

Quercetin represses apolipoprotein B expression by inhibiting the transcriptional activity of C/EBPβ.

作者信息

Shimizu Makoto, Li Juan, Inoue Jun, Sato Ryuichiro

机构信息

Department of Applied Biological Chemistry, The University of Tokyo 1-1-1 Yayoi, Bunkyo, Tokyo, Japan.

出版信息

PLoS One. 2015 Apr 15;10(4):e0121784. doi: 10.1371/journal.pone.0121784. eCollection 2015.

Abstract

Quercetin is one of the most abundant polyphenolic flavonoids found in fruits and vegetables and has anti-oxidative and anti-obesity effects. Because the small intestine is a major absorptive organ of dietary nutrients, it is likely that highly concentrated food constituents, including polyphenols, are present in the small intestinal epithelial cells, suggesting that food factors may have a profound effect in this tissue. To identify novel targets of quercetin in the intestinal enterocytes, mRNA profiling using human intestinal epithelial Caco-2 cells was performed. We found that mRNA levels of some apolipoproteins, particularly apolipoprotein B (apoB), are downregulated in the presence of quercetin. On the exposure of Caco-2 cells to quercetin, both mRNA and protein levels of apoB were decreased. Promoter analysis of the human apoB revealed that quercetin response element is localized at the 5'-proximal promoter region, which contains a conserved CCAAT enhancer-binding protein (C/EBP)-response element. We found that quercetin reduces the promoter activity of apoB, driven by the enforced expression of C/EBPβ. Quercetin had no effect on either mRNA or protein levels of C/EBPβ. In contrast, we found that quercetin inhibits the transcriptional activity of C/EBPβ but not its recruitment to the apoB promoter. On the exposure of Caco-2 cells to quercetin 3-O-glucuronide, which is in a cell-impermeable form, no notable change in apoB mRNA was observed, suggesting an intracellular action of quercetin. In vitro interaction experiments using quercetin-conjugated beads revealed that quercetin binds to C/EBPβ. Our results describe a novel regulatory mechanism of transcription of apolipoprotein genes by quercetin in the intestinal enterocytes.

摘要

槲皮素是水果和蔬菜中含量最丰富的多酚类黄酮之一,具有抗氧化和抗肥胖作用。由于小肠是膳食营养物质的主要吸收器官,包括多酚在内的高浓度食物成分可能存在于小肠上皮细胞中,这表明食物因素可能对该组织产生深远影响。为了确定槲皮素在肠道肠细胞中的新靶点,我们使用人肠上皮Caco-2细胞进行了mRNA谱分析。我们发现,在槲皮素存在的情况下,一些载脂蛋白的mRNA水平,特别是载脂蛋白B(apoB)的水平会下调。将Caco-2细胞暴露于槲皮素后,apoB的mRNA和蛋白质水平均降低。对人apoB的启动子分析表明,槲皮素反应元件位于5'-近端启动子区域,该区域包含一个保守的CCAAT增强子结合蛋白(C/EBP)反应元件。我们发现,槲皮素降低了由C/EBPβ的强制表达驱动的apoB的启动子活性。槲皮素对C/EBPβ的mRNA或蛋白质水平均无影响。相反,我们发现槲皮素抑制C/EBPβ的转录活性,但不抑制其募集到apoB启动子上。将Caco-2细胞暴露于细胞不可渗透形式的槲皮素3-O-葡萄糖醛酸后,未观察到apoB mRNA有明显变化,这表明槲皮素具有细胞内作用。使用槲皮素偶联磁珠进行的体外相互作用实验表明,槲皮素与C/EBPβ结合。我们的结果描述了槲皮素在肠道肠细胞中对载脂蛋白基因转录的一种新的调控机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be14/4398426/b37256114574/pone.0121784.g001.jpg

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