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Downregulation of IL-13 gene transcription by T-bet in human T cells.

机译:人T细胞中T-bet对IL-13基因转录的下调。

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BACKGROUND: Downregulation of a Th2 cytokine, IL-4, by a Th1-specific transcription factor, T-bet, has been demonstrated. However, the regulatory role of T-bet in another Th2 cytokine, IL-13, is not fully delineated. METHODS: IL-13 mRNA expression in Jurkat cells was examined by quantitative RT-PCR, while the transcriptional activity of 5'-flanking region in the IL-13 gene encompassing -1077 to +49 was investigated by fluorescence-based promoter reporter assay. The effect of T-bet was investigated by transfection of the cells with the T-bet expression vector. RESULTS: Stimulation with phorbol ester plus Ca2+ ionophore clearly induced IL-13 gene transcription in Jurkat cells. Ectopically expressed T-bet significantly suppressed the inducible mRNA expression and promoter activity of IL-13. CONCLUSION: IL-13 expression was downregulated by T-bet at the level of gene transcription, independently of the modulation of Th1/Th2 balance. T-bet is the potential key factor in the development of Th1/Th2-related diseases.
机译:背景:已证明Th1特异性转录因子T-bet对Th2细胞因子IL-4的下调。但是,T-bet在另一个Th2细胞因子IL-13中的调节作用尚未完全阐明。方法:采用定量RT-PCR技术检测Jurkat细胞中IL-13 mRNA的表达,并通过基于荧光的启动子报告基因检测IL-13基因5'侧翼区域的转录活性,该基因的表达范围为-1077至+49。通过用T-bet表达载体转染细胞来研究T-bet的作用。结果:佛波酯加Ca2 +离子载体刺激明显诱导Jurkat细胞中IL-13基因转录。异位表达的T-bet显着抑制了IL-13的诱导型mRNA表达和启动子活性。结论:T-bet在基因转录水平下下调了IL-13的表达,与Th1 / Th2平衡的调节无关。 T-bet是与Th1 / Th2相关疾病发展的潜在关键因素。

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