Suppr超能文献

IRF3 依赖性 RXRα 抑制在病毒感染相关肝毒性中的作用。

A role for IRF3-dependent RXRalpha repression in hepatotoxicity associated with viral infections.

作者信息

Chow Edward K, Castrillo Antonio, Shahangian Arash, Pei Liming, O'Connell Ryan M, Modlin Robert L, Tontonoz Peter, Cheng Genhong

机构信息

Molecular Biology Institute, Department of Pathology and Laboratory Medicine, Jonsson Comprehensive Cancer Center, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.

出版信息

J Exp Med. 2006 Nov 27;203(12):2589-602. doi: 10.1084/jem.20060929. Epub 2006 Oct 30.

Abstract

Viral infections and antiviral responses have been linked to several metabolic diseases, including Reye's syndrome, which is aspirin-induced hepatotoxicity in the context of a viral infection. We identify an interferon regulatory factor 3 (IRF3)-dependent but type I interferon-independent pathway that strongly inhibits the expression of retinoid X receptor alpha (RXRalpha) and suppresses the induction of its downstream target genes, including those involved in hepatic detoxification. Activation of IRF3 by viral infection in vivo greatly enhances bile acid- and aspirin-induced hepatotoxicity. Our results provide a critical link between the innate immune response and host metabolism, identifying IRF3-mediated down-regulation of RXRalpha as a molecular mechanism for pathogen-associated metabolic diseases.

摘要

病毒感染和抗病毒反应与多种代谢性疾病有关,包括瑞氏综合征,它是在病毒感染背景下由阿司匹林引起的肝毒性。我们鉴定出一条依赖干扰素调节因子3(IRF3)但不依赖I型干扰素的途径,该途径强烈抑制视黄酸X受体α(RXRα)的表达,并抑制其下游靶基因的诱导,包括那些参与肝脏解毒的基因。体内病毒感染激活IRF3会极大增强胆汁酸和阿司匹林诱导的肝毒性。我们的结果提供了先天免疫反应与宿主代谢之间的关键联系,确定IRF3介导的RXRα下调是病原体相关代谢性疾病的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f31/2118146/83a5530d29a6/jem2032589f01.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验