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ZBP1:一种强大的先天免疫传感器,也是宿主免疫的双刃剑。

ZBP1: A Powerful Innate Immune Sensor and Double-Edged Sword in Host Immunity.

机构信息

State Key Laboratory of Veterinary Etiological Biology, College of Veterinary Medicine, Lanzhou University, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou 730000, China.

出版信息

Int J Mol Sci. 2022 Sep 6;23(18):10224. doi: 10.3390/ijms231810224.

Abstract

Z-conformation nucleic acid binding protein 1 (ZBP1), a powerful innate immune sensor, has been identified as the important signaling initiation factor in innate immune response and the multiple inflammatory cell death known as PANoptosis. The initiation of ZBP1 signaling requires recognition of left-handed double-helix Z-nucleic acid (includes Z-DNA and Z-RNA) and subsequent signaling transduction depends on the interaction between ZBP1 and its adapter proteins, such as TANK-binding kinase 1 (TBK1), interferon regulatory factor 3 (IRF3), receptor-interacting serine/threonine-protein kinase 1 (RIPK1), and RIPK3. ZBP1 activated innate immunity, including type-I interferon (IFN-I) response and NF-κB signaling, constitutes an important line of defense against pathogenic infection. In addition, ZBP1-mediated PANoptosis is a double-edged sword in anti-infection, auto-inflammatory diseases, and tumor immunity. ZBP1-mediated PANoptosis is beneficial for eliminating infected cells and tumor cells, but abnormal or excessive PANoptosis can lead to a strong inflammatory response that is harmful to the host. Thus, pathogens and host have each developed multiplex tactics targeting ZBP1 signaling to maintain strong virulence or immune homeostasis. In this paper, we reviewed the mechanisms of ZBP1 signaling, the effects of ZBP1 signaling on host immunity and pathogen infection, and various antagonistic strategies of host and pathogen against ZBP1. We also discuss existent gaps regarding ZBP1 signaling and forecast potential directions for future research.

摘要

Z 构象核酸结合蛋白 1(ZBP1)是一种强大的先天免疫传感器,已被确定为先天免疫反应中重要的信号起始因子,以及多种已知的炎症细胞程序性坏死,即 PANoptosis。ZBP1 信号的起始需要识别左手双螺旋 Z 核酸(包括 Z-DNA 和 Z-RNA),随后的信号转导依赖于 ZBP1 与其衔接蛋白之间的相互作用,如 TANK 结合激酶 1(TBK1)、干扰素调节因子 3(IRF3)、受体相互作用丝氨酸/苏氨酸蛋白激酶 1(RIPK1)和 RIPK3。ZBP1 激活先天免疫,包括 I 型干扰素(IFN-I)反应和 NF-κB 信号通路,构成了抵御病原感染的重要防线。此外,ZBP1 介导的 PANoptosis 在抗感染、自身炎症性疾病和肿瘤免疫中是一把双刃剑。ZBP1 介导的 PANoptosis 有利于清除感染细胞和肿瘤细胞,但异常或过度的 PANoptosis 可导致强烈的炎症反应,对宿主有害。因此,病原体和宿主都各自发展了针对 ZBP1 信号的多重策略,以维持强大的毒力或免疫稳态。本文综述了 ZBP1 信号的机制、ZBP1 信号对宿主免疫和病原体感染的影响,以及宿主和病原体针对 ZBP1 的各种拮抗策略。我们还讨论了 ZBP1 信号存在的差距,并预测了未来研究的潜在方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f9e0/9499459/eec7650ee952/ijms-23-10224-g001.jpg

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