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Ⅰ型干扰素诱导的轨道图:亚细胞网络计划和病毒如何改变轨迹。

The Railmap of Type I Interferon Induction: Subcellular Network Plan and How Viruses Can Change Tracks.

机构信息

Junior Research Group "Cell Biology of RNA Viruses", Leibniz Institute of Virology, 20251 Hamburg, Germany.

Integrative Analysis of Pathogen-Induced Compartments, Leibniz ScienceCampus InterACt, 20251 Hamburg, Germany.

出版信息

Cells. 2022 Oct 6;11(19):3149. doi: 10.3390/cells11193149.

DOI:10.3390/cells11193149
PMID:36231111
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9563072/
Abstract

The innate immune response constitutes the cell's first line of defense against viruses and culminates in the expression of type I interferon (IFN) and IFN-stimulated genes, inducing an antiviral state in infected and neighboring cells. Efficient signal transduction is a key factor for strong but controlled type I IFN expression and depends on the compartmentalization of different steps of the signaling cascade and dynamic events between the involved compartments or organelles. This compartmentalization of the innate immune players not only relies on their association with membranous organelles but also includes the formation of supramolecular organizing centers (SMOCs) and effector concentration by liquid-liquid phase separation. For their successful replication, viruses need to evade innate defenses and evolve a multitude of strategies to impair type I IFN induction, one of which is the disruption of spatial immune signaling dynamics. This review focuses on the role of compartmentalization in ensuring an adequate innate immune response to viral pathogens, drawing attention to crucial translocation events occurring downstream of pattern recognition and leading to the expression of type I IFN. Furthermore, it intends to highlight concise examples of viral countermeasures interfering with this spatial organization to alleviate the innate immune response.

摘要

天然免疫反应构成了细胞抵御病毒的第一道防线,最终导致 I 型干扰素 (IFN) 和 IFN 刺激基因的表达,在感染和邻近细胞中诱导抗病毒状态。有效的信号转导是实现强烈但受控制的 I 型 IFN 表达的关键因素,这取决于信号级联的不同步骤在空间上的分隔以及涉及的隔室或细胞器之间的动态事件。先天免疫分子的这种分隔不仅依赖于它们与膜细胞器的关联,还包括通过液-液相分离形成超分子组织中心 (SMOC) 和效应物浓缩。为了成功复制,病毒需要逃避先天防御,并进化出多种策略来削弱 I 型 IFN 的诱导,其中之一是破坏空间免疫信号动力学。本综述重点讨论了分隔在确保对病毒病原体产生适当的先天免疫反应中的作用,提请注意发生在模式识别下游的关键易位事件,这些事件导致 I 型 IFN 的表达。此外,它旨在突出病毒对策的简明示例,这些对策干扰这种空间组织,以减轻先天免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3484/9563072/165e8f9285b8/cells-11-03149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3484/9563072/69ab9de01451/cells-11-03149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3484/9563072/165e8f9285b8/cells-11-03149-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3484/9563072/69ab9de01451/cells-11-03149-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3484/9563072/165e8f9285b8/cells-11-03149-g002.jpg

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