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神秘机制:NLRX1在病毒感染中的复杂作用

Mystery machine: the complex roles of NLRX1 in viral infection.

作者信息

Woolls Mackenzie K, Elliott Carley M, Ivester Hannah M, Allen Irving Coy

机构信息

Graduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Roanoke, VA, United States.

Biomedical and Veterinary Sciences Graduate Program, Virginia Maryland College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, United States.

出版信息

Front Immunol. 2025 Apr 28;16:1581313. doi: 10.3389/fimmu.2025.1581313. eCollection 2025.

DOI:10.3389/fimmu.2025.1581313
PMID:40356929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12066249/
Abstract

Effective antiviral immunity requires a delicate balance between controlling infection and preventing excessive inflammation. NLRX1, an atypical member of the NOD-like receptor family, plays a crucial regulatory role in this process by modulating immune responses to both RNA and DNA viruses. Unlike other NLRs, NLRX1 does not directly activate inflammatory pathways, but rather fine tunes immune responses through interactions with key signaling initiators like MAVS, FAF1, viral RNA, and FBXO6. These interactions allow NLRX1 to influence antiviral pathways in a highly context-dependent manner. In RNA virus infections, NLRX1 can either enhance immune signaling to restrict viral replication or suppress type 1 IFN responses to promote viral persistence. Similarly, in DNA viral infections, NLRX1 exerts either protective or pathogenic effects, though the precise mechanisms remain unclear. Emerging evidence suggests that NLRX1 may also serve as a key regulator of inflammation and metabolic processes during infection, further contributing to its complex role in immunity. By synthesizing current research, this review provides insight into how NLRX1 regulates immune signaling in RNA and DNA viral infections, highlighting its dynamic role in antiviral immunity and the remaining gaps in our understanding.

摘要

有效的抗病毒免疫需要在控制感染和预防过度炎症之间保持微妙的平衡。NLRX1是NOD样受体家族的一个非典型成员,通过调节对RNA和DNA病毒的免疫反应,在这一过程中发挥关键的调节作用。与其他NLR不同,NLRX1不直接激活炎症途径,而是通过与MAVS、FAF1、病毒RNA和FBXO6等关键信号启动子相互作用来微调免疫反应。这些相互作用使NLRX1能够以高度依赖环境的方式影响抗病毒途径。在RNA病毒感染中,NLRX1既可以增强免疫信号以限制病毒复制,也可以抑制1型干扰素反应以促进病毒持续存在。同样,在DNA病毒感染中,NLRX1发挥保护或致病作用,尽管确切机制尚不清楚。新出现的证据表明,NLRX1在感染过程中也可能作为炎症和代谢过程的关键调节因子,进一步促成其在免疫中的复杂作用。通过综合当前的研究,本综述深入探讨了NLRX1如何在RNA和DNA病毒感染中调节免疫信号,突出了其在抗病毒免疫中的动态作用以及我们理解中存在的差距。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/12066249/b43a727dc636/fimmu-16-1581313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/12066249/f9e0287401fb/fimmu-16-1581313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/12066249/b43a727dc636/fimmu-16-1581313-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/12066249/f9e0287401fb/fimmu-16-1581313-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c61/12066249/b43a727dc636/fimmu-16-1581313-g002.jpg

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本文引用的文献

1
An NLR family member X1 mutation (p.Arg707Cys) suppresses hepatitis B virus infection in hepatocytes and favors the interaction of retinoic acid-inducible gene 1 with mitochondrial antiviral signaling protein.一个 NLR 家族成员 X1 突变(p.Arg707Cys)抑制了肝细胞中的乙型肝炎病毒感染,并有利于维甲酸诱导基因 1 与线粒体抗病毒信号蛋白的相互作用。
Arch Virol. 2024 Nov 5;169(11):238. doi: 10.1007/s00705-024-06133-0.
2
Cellular Context Dictates the Suppression or Augmentation of Triple-Negative Mammary Tumor Metastasis by NLRX1.细胞微环境决定 NLRX1 对三阴性乳腺癌转移的抑制或增强作用。
J Immunol. 2023 Dec 15;211(12):1844-1857. doi: 10.4049/jimmunol.2200834.
3
FBXO6 regulates the antiviral immune responses via mediating alveolar macrophages survival.
FBXO6通过介导肺泡巨噬细胞存活来调节抗病毒免疫反应。
J Med Virol. 2023 Jan;95(1):e28203. doi: 10.1002/jmv.28203. Epub 2022 Oct 31.
4
NLRX1 can counteract innate immune response induced by an external stimulus favoring HBV infection by competitive inhibition of MAVS-RLRs signaling in HepG2-NTCP cells.NLRX1 可以通过在 HepG2-NTCP 细胞中竞争抑制 MAVS-RLRs 信号来抵抗外部刺激诱导的先天免疫反应,从而有利于 HBV 感染。
Sci Prog. 2021 Oct;104(4):368504211058036. doi: 10.1177/00368504211058036.
5
Anti-glomerular basement membrane disease (Goodpasture disease): From pathogenesis to plasma exchange to IdeS.抗肾小球基底膜病(Goodpasture 病):从发病机制到血浆置换再到 IdeS。
Ther Apher Dial. 2022 Feb;26(1):24-31. doi: 10.1111/1744-9987.13718. Epub 2021 Aug 10.
6
NLRX1 promotes immediate IRF1-directed antiviral responses by limiting dsRNA-activated translational inhibition mediated by PKR.NLRX1通过限制由PKR介导的双链RNA激活的翻译抑制来促进由IRF1直接引导的即时抗病毒反应。
Nat Immunol. 2017 Dec;18(12):1299-1309. doi: 10.1038/ni.3853. Epub 2017 Oct 2.
7
NLRX1 Mediates MAVS Degradation To Attenuate the Hepatitis C Virus-Induced Innate Immune Response through PCBP2.NLRX1 通过 PCBP2 介导 MAVS 降解,从而减弱丙型肝炎病毒诱导的先天免疫反应。
J Virol. 2017 Nov 14;91(23). doi: 10.1128/JVI.01264-17. Print 2017 Dec 1.
8
FAS-associated factor-1 positively regulates type I interferon response to RNA virus infection by targeting NLRX1.FAS相关因子1通过靶向NLRX1正向调节I型干扰素对RNA病毒感染的反应。
PLoS Pathog. 2017 May 22;13(5):e1006398. doi: 10.1371/journal.ppat.1006398. eCollection 2017 May.
9
NLRX1 negatively modulates type I IFN to facilitate KSHV reactivation from latency.NLRX1负向调节I型干扰素,以促进卡波西肉瘤相关疱疹病毒从潜伏期重新激活。
PLoS Pathog. 2017 May 1;13(5):e1006350. doi: 10.1371/journal.ppat.1006350. eCollection 2017 May.
10
NLRX1 Sequesters STING to Negatively Regulate the Interferon Response, Thereby Facilitating the Replication of HIV-1 and DNA Viruses.NLRX1隔离STING以负向调节干扰素反应,从而促进HIV-1和DNA病毒的复制。
Cell Host Microbe. 2016 Apr 13;19(4):515-528. doi: 10.1016/j.chom.2016.03.001.