固有免疫系统是宿主抵御病毒入侵的第一道防线.Ⅰ型干扰素是关键的抗病毒细胞因子,它在细胞建立抗病毒状态的过程中发挥了核心的作用.Ⅰ型干扰素的诱导表达是固有免疫的重要调节与效应机制.已有的研究表明:多种转录因子(NF-kappa B、ATF-2/c-Jun、IRF3、IRF7)通过在Ⅰ型干扰素的转录调控区形成稳定的转录增强复合物(enhanceosome),迅速并大量地诱导Ⅰ型干扰素表达.体内与体外的生物学分析已确立,干扰素调控因子3 (IRF3)是介导细胞表达Ⅰ型干扰素最关键的转录因子,其转录活力与生物学功能直接影响细胞的抗病毒的能力.近年来,IRF3相关的细胞信号转导与调控机制等研究取得重大进展.围绕IRF3的结构、功能以及分子调控机制等方面,概述相关的研究进展,并做前沿展望.
The innate immune system is the first line of host defense against viruses. TypeⅠ interferons (IFNs),the vital antiviral cytokines, play a critical role in establishing host antiviral state. Induction of typeⅠ IFN requires the formation of a multi-protein enhanceosome, including three families of key transcription factors (NF-κB, IRF3/7, and ATF-2/c-Jun). Transcription factor IRF3 (interferon regulatory factor 3) plays a pivotal role and is tightly regulated in this process. Recently, much progress has been made on cellular signal transduction and regulation of IRF3. Relevant advances in IRF3 biology were summarized with respect to its structure, function and regulatory mechanisms.
刘星,石贺欣,王琛.干扰素调控因子3:细胞抗病毒反应的核心转录因子[J].生物化学与生物物理进展,2010,37(8):817-825
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