Cheng Guofeng, Zhong Jin, Chung Josan, Chisari Francis V
Department of Molecular and Experimental Medicine, The Scripps Research Institute, La Jolla, CA 92037, USA.
Proc Natl Acad Sci U S A. 2007 May 22;104(21):9035-40. doi: 10.1073/pnas.0703285104. Epub 2007 May 15.
Virus infection triggers IFN immune defenses in infected cells in part through viral nucleic acid interactions, but the pathways by which dsDNA and DNA viruses trigger innate defenses are only partially understood. Here we present evidence that both retinoic acid-induced gene I (RIG-I) and mitochondrial antiviral signaling protein (MAVS) are required for dsDNA-induced IFN-beta promoter activation in a human hepatoma cell line (Huh-7), and that activation is efficiently blocked by the hepatitis C virus NS3/4A protease, which is known to block dsRNA signaling by cleaving MAVS. These findings suggest that dsDNA and dsRNA share a common pathway to trigger the innate antiviral defense response in human cells, although dsDNA appears to trigger that pathway upstream of the dsRNA-interacting protein RIG-I.
病毒感染部分通过病毒核酸相互作用在受感染细胞中触发干扰素免疫防御,但双链DNA和DNA病毒触发固有防御的途径仅得到部分了解。在此,我们提供证据表明,维甲酸诱导基因I(RIG-I)和线粒体抗病毒信号蛋白(MAVS)对于双链DNA诱导的人肝癌细胞系(Huh-7)中干扰素-β启动子激活均是必需的,并且该激活被丙型肝炎病毒NS3/4A蛋白酶有效阻断,已知该蛋白酶通过切割MAVS来阻断双链RNA信号传导。这些发现表明,双链DNA和双链RNA共享一条共同途径来触发人类细胞中的固有抗病毒防御反应,尽管双链DNA似乎在与双链RNA相互作用的蛋白RIG-I的上游触发该途径。