Antiviral Protein Viperin Promotes Toll-like Receptor 7- and Toll-like Receptor 9-Mediated Type I Interferon Production in Plasmacytoid Dendritic Cells

被引:195
作者
Saitoh, Tatsuya [1 ,2 ]
Satoh, Takashi [1 ,2 ]
Yamamoto, Naoki [3 ]
Uematsu, Satoshi [1 ,2 ]
Takeuchi, Osamu [1 ,2 ]
Kawai, Taro [1 ,2 ]
Akira, Shizuo [1 ,2 ]
机构
[1] Osaka Univ, WPI Immunol Frontier Res Ctr, Host Def Lab, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Suita, Osaka 5650871, Japan
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Microbiol, Singapore 117597, Singapore
基金
日本学术振兴会;
关键词
NF-KAPPA-B; PATTERN-RECOGNITION RECEPTORS; AMPHIPATHIC ALPHA-HELIX; INNATE IMMUNITY; GENE INDUCTION; AUTOPHAGY; ACTIVATION; VIRUS; IDENTIFICATION; RESPONSES;
D O I
10.1016/j.immuni.2011.03.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Toll-like receptor 7 (TLR7) and TLR9 sense viral nucleic acids and induce production of type I interferon (IFN) by plasmacytoid dendritic cells (pDCs) to protect the host from virus infection. We showed that the IFN-inducible antiviral protein Viperin promoted TLR7- and TLR9-mediated production of type I IFN by pDCs. Viperin expression was potently induced after TLR7 or TLR9 stimulation and Viperin localized to the cytoplasmic lipid-enriched compartments, lipid bodies, in pDCs. Viperin interacted with the signal mediators IRAK1 and TRAF6 to recruit them to the lipid bodies and facilitated K63-linked ubiquitination of IRAK1 to induce the nuclear translocation of transcription factor IRF7. Loss of Viperin reduced TLR7- and TLR9-mediated production of type I IFN by pDCs. However, Viperin was dispensable for the production of type I IFN induced by intracellular nucleic acids. Thus, Viperin mediates its antiviral function via the regulation of the TLR7 and TLR9-IRAK1 signaling axis in pDCs.
引用
收藏
页码:352 / 363
页数:12
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