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Essential role of IPS-1 in innate immune responses against RNA viruses
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Takahashi, Ken
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机构: Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan

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Yamamoto, Masahiro
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机构: Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan

Uematsu, Satoshi
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机构: Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan

Ishii, Ken J.
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机构: Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan

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Akira, Shizuo
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机构: Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan
机构:
[1] Osaka Univ, Dept Host Def, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Japan Sci & Technol Agcy, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Microbial Dis Res Inst, Combined Program Microbiol & Immunol, 21st Century COE, Suita, Osaka 5650871, Japan
关键词:
D O I:
10.1084/jem.20060792
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
IFN-beta promoter stimulator (IPS)-1 was recently identified as an adapter for retinoic acid-inducible gene I (RIG-I) and melanoma differentiation-associated gene 5 (Mda5), which recognize distinct RNA viruses. Here we show the critical role of IPS-1 in antiviral responses in vivo. IPS-1-deficient mice showed severe defects in both RIG-I- and Mda5-mediated induction of type I interferon and inflammatory cytokines and were susceptible to RNA virus infection. RNA virus-induced interferon regulatory factor-3 and nuclear factor kappa B activation was also impaired in IPS-1-deficient cells. IPS-1, however, was not essential for the responses to either DNA virus or double-stranded B-DNA. Thus, IPS-1 is the sole adapter in both RIG-I and Mda5 signaling that mediates effective responses against a variety of RNA viruses.
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页码:1795 / 1803
页数:9
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