Double-Stranded RNA Sensors and Modulators in Innate Immunity

被引:249
|
作者
Hur, Sun [1 ,2 ]
机构
[1] Harvard Med Sch, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Program Cellular & Mol Med, Boston, MA 02115 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 37, 2019 | 2019年 / 37卷
关键词
dsRNA; RIG-I-like receptor; protein kinase R; oligoadenylate synthase; dsRNA-dependent adenosine deaminase; RNA interference; PROTEIN-KINASE PKR; 2'-5' OLIGOADENYLATE SYNTHETASE; RIG-I; BINDING-PROTEIN; ADENOSINE-DEAMINASE; STRUCTURAL BASIS; DSRNA BINDING; TAR-RNA; INDUCED ACTIVATION; ANTIVIRAL ACTIVITY;
D O I
10.1146/annurev-immunol-042718-041356
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Detection of double-stranded RNAs (dsRNAs) is a central mechanism of innate immune defense in many organisms. We here discuss several families of dsRNA-binding proteins involved in mammalian antiviral innate immunity. These include RIG-I-like receptors, protein kinase R, oligoadenylate synthases, adenosine deaminases acting on RNA, RNA interference systems, and other proteins containing dsRNA-binding domains and helicase domains. Studies suggest that their functions are highly interdependent and that their interdependence could offer keys to understanding the complex regulatory mechanisms for cellular dsRNA homeostasis and antiviral immunity. This review aims to highlight their interconnectivity, as well as their commonalities and differences in their dsRNA recognition mechanisms.
引用
收藏
页码:349 / 375
页数:27
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