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Essential role of IPS-1 in innate immune responses against RNA viruses

IFN-β 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...

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Detalles Bibliográficos
Autores principales: Kumar, Himanshu, Kawai, Taro, Kato, Hiroki, Sato, Shintaro, Takahashi, Ken, Coban, Cevayir, Yamamoto, Masahiro, Uematsu, Satoshi, Ishii, Ken J., Takeuchi, Osamu, Akira, Shizuo
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118350/
https://www.ncbi.nlm.nih.gov/pubmed/16785313
http://dx.doi.org/10.1084/jem.20060792
Descripción
Sumario:IFN-β 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 κB 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.