Essential role of mda-5 in type IIFN responses to polyriboinosinic: polyribocytidylic acid and encephalomyocarditis picornavirus

被引:920
作者
Gitlin, Leonid
Barchet, Winfried
Gilfillan, Susan
Cella, Marina
Beutler, Bruce
Flavell, Richard A.
Diamond, Michael S.
Colonna, Marco
机构
[1] Washington Univ, Sch Med, Dept Med, Div Infect Dis, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[3] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[4] Yale Univ, Sch Med, Howard Hughes Med Inst, Immunobiol Sect, New Haven, CT 06520 USA
关键词
innate immunity; virus;
D O I
10.1073/pnas.0603082103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The innate immune system recognizes viral dsRNA through two distinct pathways; the Toll-like receptor 3 (TLR3) pathway detects dsRNA phagocytosed in endosomes; the helicases retinoic acid-induced protein I (RIG-I) and melanoma differentiation-associated gene-5 (mda-5) detect cytoplasmic dsRNA generated during viral replication. Both RIG-I and mda-5 can bind polyriboinosinic:polyribocytidylic acid (polyl:C), the synthetic analog of viral dsRNA, and mediate type I IFN responses to polyl:C and multiple RNA viruses in vitro. We generated mda-5-deficient mice and showed that mda-5 is the dominant receptor mediating type I IFIN secretion in response to polyl:C in vitro and in vivo. Moreover, mda-5-/- mice exhibited a selectively impaired antiviral response to encephalomyocarditis picornavirus, indicating functional specialization of mda-5 in vivo.
引用
收藏
页码:8459 / 8464
页数:6
相关论文
共 47 条
[21]   Cell type-specific involvement of RIG-I in antiviral response [J].
Kato, H ;
Sato, S ;
Yoneyama, M ;
Yamamoto, M ;
Uematsu, S ;
Matsui, K ;
Tsujimura, T ;
Takeda, K ;
Fujita, T ;
Takeuchi, O ;
Akira, S .
IMMUNITY, 2005, 23 (01) :19-28
[22]   IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction [J].
Kawai, T ;
Takahashi, K ;
Sato, S ;
Coban, C ;
Kumar, H ;
Kato, H ;
Ishii, KJ ;
Takeuchi, O ;
Akira, S .
NATURE IMMUNOLOGY, 2005, 6 (10) :981-988
[23]   Overexpression of helicard, a CARD-containing helicase cleaved during apoptosis, accelerates DNA degradation [J].
Kovacsovics, M ;
Martinon, F ;
Micheau, O ;
Bodmer, JL ;
Hofmann, K ;
Tschopp, J .
CURRENT BIOLOGY, 2002, 12 (10) :838-843
[24]   Hepatitis C virus protease NS3/4A cleaves mitochondrial antiviral signaling protein off the mitochondria to evade innate immunity [J].
Li, XD ;
Sun, LJ ;
Seth, RB ;
Pineda, G ;
Chen, ZJJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (49) :17717-17722
[25]   TLR-independent induction of dendritic cell maturation and adaptive immunity by negative-strand RNA viruses [J].
López, CB ;
Moltedo, B ;
Alexopoulou, L ;
Bonifaz, L ;
Flavell, RA ;
Moran, TM .
JOURNAL OF IMMUNOLOGY, 2004, 173 (11) :6882-6889
[26]   Subcellular localization of toll-like receptor 3 in human dendritic cells [J].
Matsumoto, M ;
Funami, K ;
Tanabe, M ;
Oshiumi, H ;
Shingai, M ;
Seto, Y ;
Yamamoto, A ;
Seya, T .
JOURNAL OF IMMUNOLOGY, 2003, 171 (06) :3154-3162
[27]   Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus [J].
Meylan, E ;
Curran, J ;
Hofmann, K ;
Moradpour, D ;
Binder, M ;
Bartenschlager, R ;
Tschopp, R .
NATURE, 2005, 437 (7062) :1167-1172
[28]   Critical role of TRAF3 in the Toll-like receptor-dependent and -independent antiviral response [J].
Oganesyan, G ;
Saha, SK ;
Guo, BC ;
He, JQ ;
Shahangian, A ;
Zarnegar, B ;
Perry, A ;
Cheng, GH .
NATURE, 2006, 439 (7073) :208-211
[29]   The immunogenic and pathogenic potential of short poly(C) tract mengo viruses [J].
Osorio, JE ;
Martin, LR ;
Palmenberg, AC .
VIROLOGY, 1996, 223 (02) :344-350
[30]   The RNA helicase Lgp2 inhibits TLR-independent sensing of viral replication by retinoic acid-inducible gene-I [J].
Rothenfusser, S ;
Goutagny, N ;
DiPerna, G ;
Gong, M ;
Monks, BG ;
Schoenemeyer, A ;
Yamamoto, M ;
Akira, S ;
Fitzgerald, KA .
JOURNAL OF IMMUNOLOGY, 2005, 175 (08) :5260-5268