Orchestrating the interferon antiviral response through the mitochondrial antiviral signaling (MAVS) adapter

被引:205
作者
Belgnaoui, S. Mehdi [1 ,2 ]
Paz, Suzanne [1 ,2 ]
Hiscott, John [1 ,3 ]
机构
[1] Jewish Gen Hosp, Lady Davis Inst, Terry Fox Mol Oncol Grp, Montreal, PQ, Canada
[2] McGill Univ, Dept Microbiol & Immunol, Montreal, PQ, Canada
[3] Vaccine & Gene Therapy Inst Florida, Port St Lucie, FL 34987 USA
基金
加拿大健康研究院;
关键词
INNATE IMMUNE-RESPONSES; E3 UBIQUITIN LIGASE; NF-KAPPA-B; RIG-I; MAMMALIAN-CELLS; PEROXISOMAL FISSION; NEGATIVE REGULATION; PROTEIN; VIRUS; RNA;
D O I
10.1016/j.coi.2011.08.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Sensing of RNA virus infection by the RIG-I-like receptors (RLRs) engages a complex signaling cascade that utilizes the mitochondrial antiviral signaling (MAVS) adapter protein to orchestrate the innate host response to pathogen, ultimately leading to the induction of antiviral and inflammatory responses mediated by type I interferon (IFN) and NF-kappa B pathways. MAVS is localized to the outer mitochondrial membrane, and has been associated with peroxisomes, the endoplasmic reticulum and autophagosomes, where it coordinates signaling events downstream of RLRs. MAVS not only plays a pivotal role in the induction of antiviral and inflammatory pathways but is also involved in the coordination of apoptotic and metabolic functions. This review summarizes recent findings related to the MAVS adapter and its essential role in the innate immune response to RNA viruses.
引用
收藏
页码:564 / 572
页数:9
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