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Tumour necrosis factor-alpha up-regulates decay-accelerating factor gene expression in human intestinal epithelial cells.

机译:肿瘤坏死因子-α上调人类肠道上皮细胞中的衰变加速因子基因表达。

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摘要

The increased expression of decay-accelerating factor (DAF) has been detected in intestinal epithelial cells at the inflamed mucosa. In this study, we examined the effects of tumour necrosis factor (TNF)-alpha on DAF expression in three intestinal epithelial cell lines. DAF mRNA expression was evaluated by Northern blot analysis, and DAF protein expression was analysed by biotin labelling and immunoprecipitation. TNF-alpha induced a marked increase in DAF mRNA and protein expression in HT-29, T84 and Caco-2 cells. In HT-29 cells, the effects of TNF-a on DAF mRNA accumulation were observed in a dose-dependent manner; DAF mRNA accumulation reached a maximum at 3-6 hr, and then gradually decreased. These effects of TNF-alpha required de novo protein synthesis. Messenger RNA stability studies suggested that TNF-alpha partially regulated DAF gene expression by a posttranscriptional mechanism. Moreover, the combination of TNF-alpha and interleukin (IL)-4 induced an additive increase in DAF mRNA accumulation in HT-29 and T84 cells. In human intestinal epithelial cells, TNF-alpha acts as a potent inducer of DAF mRNA expression, indicating an important role for TNF-alpha in the regulation of DAF expression at the inflamed mucosa.
机译:已经在发炎的粘膜的肠上皮细胞中检测到了衰变促进因子(DAF)表达的增加。在这项研究中,我们检查了肿瘤坏死因子(TNF)-α对三种肠上皮细胞系DAF表达的影响。通过Northern印迹分析评估DAF mRNA表达,并通过生物素标记和免疫沉淀分析DAF蛋白表达。 TNF-α诱导HT-29,T84和Caco-2细胞中DAF mRNA和蛋白表达显着增加。在HT-29细胞中,以剂量依赖的方式观察到TNF-α对DAF mRNA积累的影响。 DAF mRNA积累在3-6小时达到最大值,然后逐渐下降。 TNF-α的这些作用需要从头合成蛋白质。 Messenger RNA稳定性研究表明,TNF-α通过转录后机制部分调节DAF基因的表达。此外,TNF-α和白介素(IL)-4的组合诱导HT-29和T84细胞中DAF mRNA积累的累加增加。在人的肠上皮细胞中,TNF-α充当DAF mRNA表达的有效诱导剂,表明TNF-α在发炎的粘膜中调节DAF表达具有重要作用。

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