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干扰素对细胞微小RNA的调节作为一种抗病毒机制。

Interferon modulation of cellular microRNAs as an antiviral mechanism.

作者信息

Pedersen Irene M, Cheng Guofeng, Wieland Stefan, Volinia Stefano, Croce Carlo M, Chisari Francis V, David Michael

机构信息

Department of Molecular Biology, University of California San Diego, La Jolla, California 92093, USA.

出版信息

Nature. 2007 Oct 18;449(7164):919-22. doi: 10.1038/nature06205.

Abstract

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 elusive. Here we show that interferon beta (IFNbeta) rapidly modulates the expression of numerous cellular miRNAs, and that eight of these IFNbeta-induced miRNAs have sequence-predicted targets within the hepatitis C virus (HCV) genomic RNA. The introduction of synthetic miRNA-mimics corresponding to these IFNbeta-induced miRNAs reproduces the antiviral effects of IFNbeta on HCV replication and infection, whereas neutralization of these antiviral miRNAs with anti-miRNAs reduces the antiviral effects of IFNbeta against HCV. In addition, we demonstrate that IFNbeta 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 replication. Therefore, our findings strongly support the notion that mammalian organisms too, through the interferon system, use cellular miRNAs to combat viral infections.

摘要

通过非编码微小RNA(miRNA)进行的RNA干扰是植物和无脊椎动物先天抗病毒免疫反应的重要组成部分;然而,细胞miRNA在哺乳动物机体抵御病毒感染中的作用至今仍不清楚。在此我们表明,干扰素β(IFNβ)能快速调节众多细胞miRNA的表达,并且这些IFNβ诱导的miRNA中有8种在丙型肝炎病毒(HCV)基因组RNA中具有序列预测靶点。引入与这些IFNβ诱导的miRNA对应的合成miRNA模拟物可重现IFNβ对HCV复制和感染的抗病毒作用,而用抗miRNA中和这些抗病毒miRNA则会降低IFNβ对HCV的抗病毒作用。此外,我们证明IFNβ处理会导致肝脏特异性miR-122的表达显著降低,miR-122是一种先前已证明对HCV复制至关重要的miRNA。因此,我们的研究结果有力地支持了这样一种观点,即哺乳动物机体也通过干扰素系统利用细胞miRNA来对抗病毒感染。

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