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IEX-1 suppresses apoptotic damage in human intestinal epithelial Caco-2 cells induced by co-culturing with macrophage-like THP-1 cells

机译:IEX-1抑制与巨噬细胞样THP-1细胞共培养诱导的人肠上皮Caco-2细胞凋亡损伤

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摘要

We have reported previously that apoptosis of intestinal epithelial Caco-2 cells is induced by co-culturing with human macrophage-like THP-1 cells, mainly via the action of TNFα (tumour necrosis factor α) secreted from THP-1 cells [Satsu, Ishimoto, Nakano, Mochizuki, Iwanaga and Shimizu (2006) Exp. Cell Res. 312, 3909-3919]. Our recent DNA microarray analysis of co-cultured Caco-2 cells showed that IEX-1 (immediate early-response gene X-1) is the most significantly increased gene during co-culture [Ishimoto, Nakai, Satsu, Totsuka and Shimizu (2010) Biosci. Biotechnol. Biochem. 74, 437-439]. Hence, we investigated the role of IEX-1 in the co-culture-induced damage of Caco-2 cells. We showed that IEX-1 expression induced in Caco-2 cells was suppressed by anti-TNFα antibody treatment. Experiments using IEX-1-overexpressing and -knockdown Caco-2 cells suggested that IEX-1 was involved in the suppression of Caco-2 cell damage. Increases in caspase 3 activity and TNFR1 (TNF receptor 1) mRNA expression were shown in IEX-1-knockdown Caco-2 cells, suggesting that IEX-1 plays a role in the suppression of apoptosis and protects cells by controlling sensitivity to TNFα under both normal and inflammatory conditions.
机译:我们以前曾报道过,与人巨噬细胞样THP-1细胞共培养可诱导肠道上皮Caco-2细胞凋亡,主要是通过从THP-1细胞分泌的TNFα(肿瘤坏死因子α)的作用引起的。石本,中野,望月,岩永和清水(2006)Exp。 Cell Res。 312,3909-3919]。我们最近对共培养的Caco-2细胞进行的DNA芯片分析表明,共培养期间IEX-1(立即响应的早期基因X-1)是增加最明显的基因[Ishimoto,Nakai,Satsu,Totsuka和Shimizu(2010年) )Biosci。生物技术。生化。 74,437-439]。因此,我们研究了IEX-1在共培养诱导的Caco-2细胞损伤中的作用。我们表明,抗TNFα抗体处理可抑制Caco-2细胞中诱导的IEX-1表达。使用IEX-1过表达和敲低Caco-2细胞的实验表明,IEX-1参与了Caco-2细胞损伤的抑制。在IEX-1敲​​低的Caco-2细胞中显示了caspase 3活性和TNFR1(TNF受体1)mRNA表达的增加,这表明IEX-1在抑制凋亡的过程中发挥了作用,并通过控制在两种情况下对TNFα的敏感性来保护细胞正常和发炎的情况。

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