PKR-dependent mechanisms of interferon-α for inhibiting hepatitis B virus replication.

Abstract

Interferon-α (IFN-α) inhibits the replication of hepatitis B virus (HBV) in vivo and in vitro, but the molecular mechanism of this inhibition has been elusive. We found that while HBV replication in transfected human hepatoma Huh-7 cell was severely inhibited by IFN-α treatment as reported previously, this inhibition was markedly impaired in the cell in which the expression of IFN-inducible, double-stranded RNA-dependent protein kinase (PKR) was stably and specifically suppressed through RNA-interference. Intracellular level of viral capsids was down-regulated likewise in a PKR-dependent manner, whereas that of HBV transcripts including the viral RNA pregenome was not affected by IFN-α treatment. Ectopic expression of PKR also resulted in the reduction of viral capsids with concomitant increase of phosphorylated eIF2α. These results suggested that PKR functions as a key mediator of IFN-α in opposing HBV replication, most likely through the inhibition of protein synthesis.

DOI: 10.1007/s10059-011-1059-6
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@article{Park2011PKRdependentMO, title={PKR-dependent mechanisms of interferon-α for inhibiting hepatitis B virus replication.}, author={Il-Hyun Park and Kyung-won Baek and Eun-Young Cho and Byung-Yoon Ahn}, journal={Molecules and cells}, year={2011}, volume={32 2}, pages={167-72} }