Chang Ming Xian
State Key Laboratory of Freshwater Ecology and Biotechnology, Key Laboratory of Aquaculture Disease Control, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, Hubei Province, 430072, China; Innovation Academy for Seed Design, Chinese Academy of Sciences, Beijing, China; University of Chinese Academy of Sciences, Beijing, China.
Dev Comp Immunol. 2021 Jun;119:104038. doi: 10.1016/j.dci.2021.104038. Epub 2021 Feb 4.
At each stage of innate immune response, there are stimulatory and inhibitory signals that modulate the strength and character of the response. RIG-I-like receptor (RLR) signaling pathway plays pivotal roles in antiviral innate immune response. Recent studies have revealed the molecular mechanisms that viral infection leads to the activation of RLRs-mediated downstream signaling cascades and the production of type I interferons (IFNs). However, antiviral immune responses must be tightly regulated in order to prevent detrimental type I IFNs production. Previous reviews have highlighted negative regulation of RLR signaling pathway, which mainly target to directly regulate RIG-I, MDA5, MAVS and TBK1 function in mammals. In this review, we summarize recent advances in our understanding of negative regulators of RLR signaling pathway in teleost, with specific focus on piscine and viral regulatory mechanisms that directly or indirectly inhibit the function of RIG-I, MDA5, LGP2, MAVS, TRAF3, TBK1, IRF3 and IRF7 both in the steady state or upon viral infection. We also further discuss important directions for future studies, especially for non-coding RNAs and post-translational modifications via fish specific TRIM proteins. The knowledge of negative regulators of RLR signaling pathway in teleost will shed new light on the critical information for potential therapeutic purposes.
在天然免疫反应的每个阶段,都存在刺激和抑制信号,这些信号调节反应的强度和特征。维甲酸诱导基因I样受体(RLR)信号通路在抗病毒天然免疫反应中起关键作用。最近的研究揭示了病毒感染导致RLR介导的下游信号级联激活和I型干扰素(IFN)产生的分子机制。然而,抗病毒免疫反应必须受到严格调控,以防止产生有害的I型干扰素。以往的综述强调了RLR信号通路的负调控,其主要针对直接调节哺乳动物中维甲酸诱导基因I、黑色素瘤分化相关基因5、线粒体抗病毒信号蛋白和TANK结合激酶1的功能。在本综述中,我们总结了硬骨鱼中RLR信号通路负调控因子的最新研究进展,特别关注硬骨鱼和病毒的调控机制,这些机制在稳态或病毒感染时直接或间接抑制维甲酸诱导基因I、黑色素瘤分化相关基因5、实验室遗传学和生理学2、线粒体抗病毒信号蛋白、肿瘤坏死因子受体相关因子3、TANK结合激酶1、干扰素调节因子3和干扰素调节因子7的功能。我们还进一步讨论了未来研究的重要方向,特别是关于非编码RNA和通过鱼类特异性TRIM蛋白进行的翻译后修饰。硬骨鱼中RLR信号通路负调控因子的知识将为潜在治疗目的的关键信息提供新的线索。