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辛酸和中链甘油三酯抑制Caco-2细胞中白细胞介素-8基因的转录:与强效组蛋白脱乙酰酶抑制剂曲古抑菌素A的比较。

Caprylic acid and medium-chain triglycerides inhibit IL-8 gene transcription in Caco-2 cells: comparison with the potent histone deacetylase inhibitor trichostatin A.

作者信息

Hoshimoto Aihiro, Suzuki Yasuo, Katsuno Tatsuro, Nakajima Hiroshi, Saito Yasushi

机构信息

Department of Clinical Cell Biology, Graduate School of Medicine, Chiba University, Chiba, Japan.

出版信息

Br J Pharmacol. 2002 May;136(2):280-6. doi: 10.1038/sj.bjp.0704719.

Abstract
  1. Medium-chain triglyceride (MCT) is often administered to patients with Crohn's disease (CD) or short-bowel syndrome. However, little is known about the effects of medium-chain fatty acids (MCFAs) and MCT on intestinal inflammation. In this study we examined whether caprylic acid, one of the MCFAs, and MCT suppress IL-8 secretion by differentiated Caco-2 cells. 2. We found for the first time that caprylic acid and MCT suppress IL-8 secretion by Caco-2 cells at the transcriptional level when precultured together for 24 h. We also tried to clarify the mechanism of IL-8 gene inhibition by examining the activation of NF-kappaB and other transcription factors by electrophoretic mobility shift assay (EMSA), and found that caprylic acid did not modulate their activation. 3. The result of dual-luciferase assay using Caco-2 cells transfected with IL-8 promoter/luciferase reporter plasmid revealed that caprylic acid inhibited the activation of IL-8 promoter. 4. Similar results were observed when cells were precultured with the well-known potent histone deacetylase inhibitor trichostatin A (TSA). 5. We examined the state of H4 acetylation in IL-8 promoter using the technique known as chromatin immunoprecipitation (Chr-IP). TSA rapidly induced H4 acetylation in IL-8 promoter chromatin, whereas caprylic acid did not. These results suggest that the inhibition of IL-8 gene transcription induced by caprylic acid and TSA does not necessarily require the marked suppression of transcription factors, and the mechanism of inhibition of IL-8 gene transcription may be different between caprylic acid and TSA.
摘要
  1. 中链甘油三酯(MCT)常用于克罗恩病(CD)或短肠综合征患者。然而,关于中链脂肪酸(MCFAs)和MCT对肠道炎症的影响知之甚少。在本研究中,我们检测了MCFAs之一的辛酸以及MCT是否能抑制分化的Caco-2细胞分泌白细胞介素-8(IL-8)。2. 我们首次发现,辛酸和MCT在共同预培养24小时时,能在转录水平抑制Caco-2细胞分泌IL-8。我们还试图通过电泳迁移率变动分析(EMSA)检测核因子κB(NF-κB)和其他转录因子的激活情况,以阐明IL-8基因抑制的机制,结果发现辛酸并未调节它们的激活。3. 使用转染了IL-8启动子/荧光素酶报告质粒的Caco-2细胞进行双荧光素酶分析的结果显示,辛酸抑制了IL-8启动子的激活。4. 当细胞与著名的强效组蛋白去乙酰化酶抑制剂曲古抑菌素A(TSA)共同预培养时,观察到了类似的结果。5. 我们使用染色质免疫沉淀(Chr-IP)技术检测了IL-8启动子中组蛋白H4的乙酰化状态。TSA能迅速诱导IL-8启动子染色质中H4的乙酰化,而辛酸则不能。这些结果表明,辛酸和TSA诱导的IL-8基因转录抑制不一定需要显著抑制转录因子,并且辛酸和TSA抑制IL-8基因转录的机制可能不同。

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