MDA5/RIG-I and virus recognition

被引:485
作者
Takeuchi, Osamu [1 ]
Akira, Shizuo [1 ]
机构
[1] Osaka Univ, Host Def Lab, WPI Immunol Frontier Res Ctr, Suita, Osaka 5650871, Japan
关键词
D O I
10.1016/j.coi.2008.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The innate immune system initially recognizes RNA virus infection and evokes antiviral responses by producing type I interferons (IFNs). Toll-like receptors (TLRs) and cytoplasmic retinoic acid-inducible gene I (RIG-I)-like helicases (RLHs) are the two major receptor systems for detecting RNA viruses. The RLH signaling pathways play essential roles in the recognition of RNA viruses in various cells, with the exception of plasmacytoid dendritic cells, which utilize TLRs for virus recognition. The route of infection determines the cell types responsible for type I IFN production. Recent studies have suggested that TLRs are critical for activation of adaptive immune responses against several virus infections, although it may be premature to draw such a conclusion for virus infections in general. In this review, we will discuss recent advances toward clarifying the signaling pathways activated by RLHs and TLRs.
引用
收藏
页码:17 / 22
页数:6
相关论文
共 48 条
  • [1] Pathogen recognition and innate immunity
    Akira, S
    Uematsu, S
    Takeuchi, O
    [J]. CELL, 2006, 124 (04) : 783 - 801
  • [2] Negative regulation of the RIG-I signaling by the ubiquitin ligase RNF125
    Arimoto, Kei-ichiro
    Takahashi, Hitoshi
    Hishiki, Takayuki
    Konishi, Hicleyuki
    Fujita, Takashi
    Shimotohno, Kunitada
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (18) : 7500 - 7505
  • [3] Genetic analysis of resistance to viral infection
    Beutler, Bruce
    Eidenschenk, Celine
    Crozat, Karine
    Imler, Jean-Luc
    Takeuchi, Osamu
    Hoffmann, Jules A.
    Akira, Shizuo
    [J]. NATURE REVIEWS IMMUNOLOGY, 2007, 7 (10) : 753 - 766
  • [4] IKKε and TBK1 are essential components of the IRF3 signaling pathway
    Fitzgerald, KA
    McWhirter, SM
    Faia, KL
    Rowe, DC
    Latz, E
    Golenbock, DT
    Coyle, AJ
    Liao, SM
    Maniatis, T
    [J]. NATURE IMMUNOLOGY, 2003, 4 (05) : 491 - 496
  • [5] Establishment and maintenance of the innate antiviral response to west nile virus involves both RIG-I and MDA5 signaling through IPS-1
    Fredericksen, Brenda L.
    Keller, Brian C.
    Fornek, Jamie
    Katze, Michael G.
    Gale, Michael, Jr.
    [J]. JOURNAL OF VIROLOGY, 2008, 82 (02) : 609 - 616
  • [6] TRIM25 RING-finger E3 ubiquitin ligase is essential for RIG-I-mediated antiviral activity
    Gack, Michaela U.
    Shin, Young C.
    Joo, Chul-Hyun
    Urano, Tomohiko
    Liang, Chengyu
    Sun, Lijun
    Takeuchi, Osamu
    Akira, Shizuo
    Chen, Zhijian
    Inoue, Satoshi
    Jung, Jae U.
    [J]. NATURE, 2007, 446 (7138) : 916 - U2
  • [7] Essential role of mda-5 in type IIFN responses to polyriboinosinic: polyribocytidylic acid and encephalomyocarditis picornavirus
    Gitlin, Leonid
    Barchet, Winfried
    Gilfillan, Susan
    Cella, Marina
    Beutler, Bruce
    Flavell, Richard A.
    Diamond, Michael S.
    Colonna, Marco
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (22) : 8459 - 8464
  • [8] Modulation of the interferon antiviral response by the TBK1/IKKi adaptor protein TANK
    Guo, Beichu
    Cheng, Genhong
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (16) : 11817 - 11826
  • [9] Specificity in Toll-like receptor signalling through distinct effector functions of TRAF3 and TRAF6
    Häcker, H
    Redecke, V
    Blagoev, B
    Kratchmarova, I
    Hsu, LC
    Wang, GG
    Kamps, MP
    Raz, E
    Wagner, H
    Häcker, G
    Mann, M
    Karin, M
    [J]. NATURE, 2006, 439 (7073) : 204 - 207
  • [10] IRF-7 is the master regulator of type-I interferon-dependent immune responses
    Honda, K
    Yanai, H
    Negishi, H
    Asagiri, M
    Sato, M
    Mizutani, T
    Shimada, N
    Ohba, Y
    Takaoka, A
    Yoshida, N
    Taniguchi, T
    [J]. NATURE, 2005, 434 (7034) : 772 - 777