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核因子κB与干扰素调节因子1发生物理相互作用,并协同诱导主要组织相容性复合体I类基因的表达。

NF kappa B and interferon regulatory factor 1 physically interact and synergistically induce major histocompatibility class I gene expression.

作者信息

Drew P D, Franzoso G, Becker K G, Bours V, Carlson L M, Siebenlist U, Ozato K

机构信息

Neuroimmunology Branch, National Institute of Neurological Diseases and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

出版信息

J Interferon Cytokine Res. 1995 Dec;15(12):1037-45. doi: 10.1089/jir.1995.15.1037.

Abstract

Major histocompatibility (MHC) class I gene expression is synergistically induced by the cytokines TNF-alpha and IFN-gamma. However, the mechanism that results in synergistic activation of these genes has remained unclear. We demonstrated here that TNF-alpha induced binding of NF kappa B p50 and p65 to the NF kappa B-like element of the MHC class I promoter termed region I and IFN-gamma induced binding of IRF-1 to the adjacent interferon consensus sequence (ICS). We further demonstrated that NF kappa B and IRF-1 physically interacted with each other and cooperatively induced MHC class I gene expression when cotransfected into CHP-126 neuroblastomas. These results provide a molecular mechanism by which TNF-alpha and IFN-gamma synergistically induce the expression of a variety of genes involved in immune responses, including MHC class I.

摘要

主要组织相容性复合体(MHC)I类基因的表达是由细胞因子肿瘤坏死因子-α(TNF-α)和干扰素-γ(IFN-γ)协同诱导的。然而,导致这些基因协同激活的机制仍不清楚。我们在此证明,TNF-α诱导核因子κB p50和p65与MHC I类启动子的核因子κB样元件(称为区域I)结合,而IFN-γ诱导干扰素调节因子-1(IRF-1)与相邻的干扰素共有序列(ICS)结合。我们进一步证明,当共转染到CHP-126神经母细胞瘤中时,核因子κB和IRF-1相互发生物理作用并协同诱导MHC I类基因表达。这些结果提供了一种分子机制,通过该机制TNF-α和IFN-γ协同诱导包括MHC I类在内的多种参与免疫反应的基因的表达。

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