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前沿:促炎细胞因子对干扰素调节因子-1和多聚免疫球蛋白受体的协同调节

Cutting edge: coordinate regulation of IFN regulatory factor-1 and the polymeric Ig receptor by proinflammatory cytokines.

作者信息

Blanch V J, Piskurich J F, Kaetzel C S

机构信息

Department of Microbiology/Immunology, University of Kentucky, Lexington, KY 40536, USA.

出版信息

J Immunol. 1999 Feb 1;162(3):1232-5.

PMID:9973374
Abstract

The polymeric IgR (pIgR) mediates transcytosis of IgA across epithelial barriers of mucous membranes and exocrine glands. Synthesis of pIgR is up-regulated by the proinflammatory cytokines TNF-alpha, IFN-gamma, and IL-1 in HT-29 human colon carcinoma cells. We previously reported that IFN-gamma and TNF-alpha induce production of the transcription factor IFN regulatory factor-1 (IRF-1) in HT-29 cells and that IRF-1 binds to an element in exon 1 of the PIGR gene. We now report that levels of IRF-1 and pIgR mRNA are coordinately regulated in HT-29 cells by TNF-alpha, IFN-gamma, and IL-1beta. Furthermore, we demonstrate that in vivo expression of pIgR mRNA is greatly depressed in the intestine and liver of IRF-1-deficient mice. Our findings indicate a major role for the IRF-1 transcription factor in regulation of the PIGR gene and suggest a model for regulation of important genes in the mucosal immune system by proinflammatory cytokines.

摘要

聚合免疫球蛋白受体(pIgR)介导IgA跨粘膜和外分泌腺上皮屏障的转胞吞作用。在HT - 29人结肠癌细胞中,促炎细胞因子TNF-α、IFN-γ和IL-1可上调pIgR的合成。我们之前报道过,IFN-γ和TNF-α可诱导HT - 29细胞中转录因子干扰素调节因子-1(IRF-1)的产生,且IRF-1可与PIGR基因外显子1中的一个元件结合。我们现在报道,TNF-α、IFN-γ和IL-1β可协同调节HT - 29细胞中IRF-1和pIgR mRNA的水平。此外,我们证明,在IRF-1缺陷小鼠的肠道和肝脏中,pIgR mRNA的体内表达显著降低。我们的研究结果表明IRF-1转录因子在PIGR基因调控中起主要作用,并提出了一种促炎细胞因子调节粘膜免疫系统重要基因的模型。

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