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先天免疫信号中的核酸-蛋白凝聚物。

Nucleic acid-protein condensates in innate immune signaling.

机构信息

Department of Biochemistry, University of Colorado, Boulder, CO, USA.

Howard Hughes Medical Institute, Chevy Chase, MD, USA.

出版信息

EMBO J. 2023 Apr 3;42(7):e111870. doi: 10.15252/embj.2022111870. Epub 2022 Sep 30.

Abstract

The presence of foreign nucleic acids in the cytosol is a marker of infection. Cells have sensors, also known as pattern recognition receptors (PRRs), in the cytosol that detect foreign nucleic acid and initiate an innate immune response. Recent studies have reported the condensation of multiple PRRs including PKR, NLRP6, and cGAS, with their nucleic acid activators into discrete nucleoprotein assemblies. Nucleic acid-protein condensates form due to multivalent interactions and can create high local concentrations of components. The formation of PRR-containing condensates may alter the magnitude or timing of PRR activation. In addition, unique condensates form following RNase L activation or during paracrine signaling from virally infected cells that may play roles in antiviral defense. These observations suggest that condensate formation may be a conserved mechanism that cells use to regulate activation of the innate immune response and open an avenue for further investigation into the composition and function of these condensates. Here we review the nucleic acid-protein granules that are implicated in the innate immune response, discuss general consequences of condensate formation and signal transduction, as well as what outstanding questions remain.

摘要

细胞质中外源核酸的存在是感染的标志。细胞质中的细胞传感器,也称为模式识别受体(PRR),可识别外源核酸并启动先天免疫反应。最近的研究报告称,包括 PKR、NLRP6 和 cGAS 在内的多种 PRR 与其核酸激活剂在细胞质中凝聚成离散的核蛋白组装体。核酸-蛋白凝聚物的形成是由于多价相互作用,可以在局部形成高浓度的成分。含有 PRR 的凝聚物的形成可能会改变 PRR 激活的幅度或时间。此外,在 RNase L 激活或病毒感染细胞旁分泌信号传导期间会形成独特的凝聚物,这可能在抗病毒防御中发挥作用。这些观察结果表明,凝聚物的形成可能是细胞用来调节先天免疫反应激活的保守机制,并为进一步研究这些凝聚物的组成和功能开辟了途径。在这里,我们回顾了参与先天免疫反应的核酸-蛋白颗粒,讨论了凝聚物形成和信号转导的一般后果,以及仍然存在哪些悬而未决的问题。

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