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Antiviral signaling through pattern recognition receptors
被引:344
作者:
Kawai, Taro
Akira, Shizuo
机构:
[1] Japan Sci & Technol Agcy, Dept Host Def, Res Inst Microbial Dis, Suita, Osaka 5650871, Japan
[2] Japan Sci & Technol Agcy, ERATO, Res Inst Microbial Dis, Suita, Osaka 5650871, Japan
关键词:
innate immunity;
virus infection;
Toll-like receptor;
RIG-I-like RNA helicase;
signal transduction;
NF-KAPPA-B;
HEPATITIS-C-VIRUS;
TOLL-LIKE RECEPTOR-3;
PLASMACYTOID DENDRITIC CELLS;
DOUBLE-STRANDED-RNA;
INNATE IMMUNE-RESPONSES;
INTERFERON-ALPHA PRODUCTION;
GENE INDUCTION-PROGRAM;
RIG-I;
ADAPTER PROTEIN;
D O I:
10.1093/jb/mvm032
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Viral infection is detected by the host innate immune system. Innate immune cells such as dendritic cells and macrophages detect nucleic acids derived from viruses through pattern recognition receptors (PRRs). Viral recognition by PRRs initiates the activation of signaling pathways that lead to production of type I interferon and inflammatory cytokines, which are important for the elimination of viruses. Two types of PRRs that recognize viral nucleic acids, Toll-like receptors (TLR) and RIG-1like RNA helicases (RLH), have been identified. Of the TLRs, TLR3 recognizes viral double-stranded (ds) RNA, TLR7 and human TLR8 identify viral single-stranded (ss) RNA and TLR9 detects viral DNA. TLRs are located in endosomal compartments, whereas RLH are present in the cytoplasm where they detect viral dsRNA or ssRNA. Here we review the role of TLRs and RLHs in the antiviral innate immune response.
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页码:137 / 145
页数:9
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