Targeting of the cGAS-STING system by DNA viruses

被引:30
作者
Phelan, Thomas [1 ]
Little, Mark A. [1 ,2 ]
Brady, Gareth [1 ]
机构
[1] Trinity Coll Dublin, Trinity Hlth Kidney Ctr, Trinity Translat Med Inst, St James Hosp Campus, Dublin, Ireland
[2] Trinity Coll Dublin, Irish Ctr Vasc Biol, Dublin, Ireland
基金
英国惠康基金; 爱尔兰科学基金会;
关键词
cGAS; STING; DNA virus; NF-kappa B; IRF; NF-KAPPA-B; HERPES-SIMPLEX-VIRUS; CYCLIC GMP-AMP; HUMAN CYTOMEGALOVIRUS; GENE INDUCTION; PROTEIN; ACTIVATION; INTERFERON; ADAPTER; KINASE;
D O I
10.1016/j.bcp.2020.113831
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Innate sensing of viruses by cytosolic nucleic acid sensors is a key feature of anti-viral immunity against these pathogens. The DNA sensing pathway through the sensor cyclic GMP-AMP synthase (cGAS) and its downstream effector stimulator of interferon genes (STING) has emerged in recent years as a key, front-line means of driving interferons and pro-inflammatory cytokines in response to DNA virus infection in vertebrates. Unsurprisingly, many DNA viruses have evolved effective inhibitors of this signalling system which target at a wide variety of points from sensing all the way down to the activation of Interferon Regulatory Factor (IRF)-family and Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B)-family transcription factors which drive a program of pro-inflammatory and anti-viral gene expression. Here we review DNA viruses that have been shown to inhibit this pathway and the inhibitors they have evolved to do it.
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页数:9
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