植物和無脊椎動物能在病毒感染中將RNA沉默用作一種保護(hù)機(jī)制?，F(xiàn)在，細(xì)胞微RNA也被發(fā)現(xiàn)在哺乳動物細(xì)胞中有一種抗病毒功能,。β-干擾素參與人體細(xì)胞中若干種細(xì)胞微RNA的調(diào)控,，其中的8種對于抵抗丙肝病毒上的序列具有活性,。此外,，細(xì)胞微RNA水平的調(diào)控還被發(fā)現(xiàn)能夠顯著改變β-干擾素的抗病毒效應(yīng),，說明它們是哺乳動物先天免疫反應(yīng)體系的一個功能性構(gòu)成部分。
原始出處:
Nature 449, 919-922 (18 October 2007) | doi:10.1038/nature06205; Received 26 July 2007; Accepted 29 August 2007
Interferon modulation of cellular microRNAs as an antiviral mechanism
Irene M. Pedersen1, Guofeng Cheng3, Stefan Wieland3, Stefano Volinia4, Carlo M. Croce4, Francis V. Chisari3 & Michael David1,2
Department of Molecular Biology,
Division of Biological Sciences, and,
Moores Cancer Center, University of California San Diego, La Jolla, California 92093, USA
Division of Experimental Pathology, The Scripps Research Institute, La Jolla, California 92037, USA
Department of Molecular Virology, Immunology & Medical Genetics, Ohio State University, Columbus, Ohio 43210, USA
Correspondence to: Michael David1,2 Correspondence and requests for materials should be addressed to M.D. (Email: [email protected]).
RNA interference through non-coding microRNAs (miRNAs) represents a vital component of the innate antiviral immune response in plants and invertebrate animals; however, a role for cellular miRNAs in the defence against viral infection in mammalian organisms has thus far remained elusive1. Here we show that interferon beta (IFN) rapidly modulates the expression of numerous cellular miRNAs, and that eight of these IFN-induced miRNAs have sequence-predicted targets within the hepatitis C virus (HCV) genomic RNA. The introduction of synthetic miRNA-mimics corresponding to these IFN-induced miRNAs reproduces the antiviral effects of IFN on HCV replication and infection, whereas neutralization of these antiviral miRNAs with anti-miRNAs reduces the antiviral effects of IFN against HCV. In addition, we demonstrate that IFN treatment leads to a significant reduction in the expression of the liver-specific miR-122, an miRNA that has been previously shown to be essential for HCV replication2. Therefore, our findings strongly support the notion that mammalian organisms too, through the interferon system, use cellular miRNAs to combat viral infections.
