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MDA5 and LGP2: Accomplices and Antagonists of Antiviral Signal Transduction
被引:96
作者:
Rodriguez, Kenny R.
[1
]
Bruns, Annie M.
[1
]
Horvath, Curt M.
[1
]
机构:
[1] Northwestern Univ, Dept Mol Biosci, Evanston, IL 60208 USA
关键词:
DOUBLE-STRANDED-RNA;
I-LIKE RECEPTORS;
INDUCIBLE GENE-I;
PARAMYXOVIRUS V-PROTEINS;
INNATE IMMUNE-RESPONSES;
IFN-BETA PROMOTER;
NF-KAPPA-B;
RIG-I;
STRUCTURAL BASIS;
HELICASE LGP2;
D O I:
10.1128/JVI.00640-14
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Mammalian cells have the ability to recognize virus infection and mount a powerful antiviral transcriptional response that provides an initial barrier to replication and impacts both innate and adaptive immune responses. Retinoic acid-inducible gene I (RIG-I)-like receptor (RLR) proteins mediate intracellular virus recognition and are activated by viral RNA ligands to induce antiviral signal transduction. While the mechanisms of RIG-I regulation are already well understood, less is known about the more enigmatic melanoma differentiation-associated 5 (MDA5) and laboratory of genetics and physiology 2 (LGP2). Emerging evidence suggests that these two RLRs are intimately associated as both accomplices and antagonists of antiviral signal transduction.
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页码:8194 / 8200
页数:7
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