| Literature DB >> 23399035 |
Lumin Zhang1, Harvey J Alter, Haiping Wang, Shuaizheng Jia, Ena Wang, Francesco M Marincola, James W-K Shih, Richard Y Wang.
Abstract
Protein kinase R (PKR), a sensor of double-stranded RNA, plays an important role in the host response to viral infection. Hepatitis C genotype 2a virus (HCV2a) has been shown to induce PKR activation to suppress the translation of antiviral interferon stimulated genes (ISGs), suggesting that PKR inhibitor can be beneficial for treating chronically HCV-infected patients in conjunction with interferon alpha and ribavirin. However, in this study, we found that PKR inhibition using siRNA PKR, shRNA PKR or PKR inhibitor enhanced HCV 1a replication and rendered Huh7.5.1 cells more susceptible to HCV1a infection. Additionally, PKR silencing suppressed NF-kB activation and NF-kB mediated STAT1 phosphorylation in Huh7.5.1 cells and HCV1a persistently infected Huh7.5.1 cells (2HDD4). These effects were accompanied by a reduction of interferon beta response and thereby enhanced HCV1a replication in Huh7.5.1 cells. We conclude that host cells can employ PKR activation to restrict HCV1a replication through regulation of NF-kB expression. Published by Elsevier Inc.Entities:
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Year: 2013 PMID： 23399035 PMCID： PMC3594529 DOI： 10.1016/j.virol.2013.01.015
Source DB: PubMed Journal: Virology ISSN： 0042-6822 Impact factor: 3.616