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3,5,7,3',4'-五甲氧基黄酮通过转录调控人肠道 Caco-2 细胞紧密连接增强屏障功能。

3,5,7,3',4'-Pentamethoxyflavone Enhances the Barrier Function through Transcriptional Regulation of the Tight Junction in Human Intestinal Caco-2 Cells.

机构信息

Graduate School of Biosphere Science, Hiroshima University, 1-4-4 Kagamiyama, Higashi-Hiroshima 739-8528, Japan.

Faculty of Agricultural Technology, Gadjah Mada University, Jl. Flora No 1, Depok, Sleman, Yogyakarta 55281, Indonesia.

出版信息

J Agric Food Chem. 2021 Sep 8;69(35):10174-10183. doi: 10.1021/acs.jafc.1c04295. Epub 2021 Aug 27.

Abstract

The intestinal tight junction (TJ) barrier plays a pivotal role in the regulation of intestinal homeostasis. This study investigated the effects of 3,5,7,3',4'-pentamethoxyflavone (PMF), a major polymethoxyflavone found in black ginger, on TJ barrier regulation using intestinal Caco-2 cells. PMF treatment enhanced the TJ barrier integrity in Caco-2 cells, indicated by increased transepithelial electrical resistance (control, 1261 ± 36 Ω·cm; 100 μM PMF, 1383 ± 55 Ω·cm at 48 h, < 0.05) and decreased permeability to fluorescein-conjugated dextran (control, 24.2 ± 1.8 pmol/(cm × h); 100 μM PMF, 18.6 ± 1.0 pmol/(cm × h), < 0.05). Immunoblot analysis revealed that PMF increased the cytoskeletal association and cellular expression of the TJ proteins, zonula occludens-1, claudin-3, and claudin-4 (e.g., occludin; control, 1.00 ± 0.2; 100 μM PMF, 3.69 ± 0.86 at 48 h, < 0.05). Quantitative reverse transcriptase-polymerase chain reaction analysis and a luciferase promoter assay showed that PMF enhanced the transcription of occludin, claudin-3, and claudin-4. The promoter assay with site-directed mutagenesis indicated that PMF-induced occludin and claudin-3 transcription was mediated by transcription factors, KLF5 and EGR1, respectively, while PMF activated claudin-4 transcription through GATA1 and AP1. Taken together, the transcriptional regulation of TJ proteins is involved in PMF-mediated promotion of the intestinal barrier .

摘要

肠道紧密连接 (TJ) 屏障在调节肠道内稳态方面发挥着关键作用。本研究使用肠道 Caco-2 细胞研究了 3,5,7,3',4'-五甲氧基黄酮 (PMF),一种黑姜中发现的主要多甲氧基黄酮,对 TJ 屏障调节的影响。PMF 处理增强了 Caco-2 细胞中的 TJ 屏障完整性,表现为跨上皮电阻增加(对照,1261 ± 36 Ω·cm;100 μM PMF 在 48 小时时为 1383 ± 55 Ω·cm, < 0.05)和荧光素结合葡聚糖的通透性降低(对照,24.2 ± 1.8 pmol/(cm × h);100 μM PMF,18.6 ± 1.0 pmol/(cm × h), < 0.05)。免疫印迹分析显示,PMF 增加了 TJ 蛋白,紧密连接蛋白-1、闭合蛋白-3 和闭合蛋白-4 的细胞表达和细胞骨架关联(例如,闭合蛋白;对照,1.00 ± 0.2;100 μM PMF 在 48 小时时为 3.69 ± 0.86, < 0.05)。定量逆转录-聚合酶链反应分析和荧光素酶启动子测定表明,PMF 增强了闭合蛋白-1、闭合蛋白-3 和闭合蛋白-4 的转录。具有定点突变的启动子测定表明,PMF 诱导的闭合蛋白和闭合蛋白-3 转录分别由转录因子 KLF5 和 EGR1 介导,而 PMF 通过 GATA1 和 AP1 激活闭合蛋白-4 转录。总之,TJ 蛋白的转录调节参与了 PMF 介导的肠道屏障促进作用。

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