Regulation of Interferon Regulatory Factor-3 by the Hepatitis C Virus Serine Protease
The University of Texas Medical Branch at Galveston · The University of Texas Southwestern Medical Center
Abstract
Persistent infections with hepatitis C virus (HCV) are likely to depend on viral inhibition of host defenses. We show that the HCV NS3/4A serine protease blocks the phosphorylation and effector action of interferon regulatory factor-3 (IRF-3), a key cellular antiviral signaling molecule. Disruption of NS3/4A protease function by mutation or a ketoamide peptidomimetic inhibitor relieved this blockade and restored IRF-3 phosphorylation after cellular challenge with an unrelated virus. Furthermore, dominant-negative or constitutively active IRF-3 mutants, respectively, enhanced or suppressed HCV RNA replication in hepatoma cells. Thus, the NS3/4A protease represents a dual therapeutic target, the inhibition of…
Citation impact
- FWCI
- 38.68
- Percentile
- 100%
- References
- 25
Authors
7- EFEileen FoyCorresponding
The University of Texas Medical Branch at Galveston, The University of Texas Southwestern Medical Center
- KLKui Li
The University of Texas Medical Branch at Galveston, The University of Texas Southwestern Medical Center
- CWChunfu Wang
The University of Texas Medical Branch at Galveston, The University of Texas Southwestern Medical Center
- RSRhea Sumpter
The University of Texas Medical Branch at Galveston, The University of Texas Southwestern Medical Center
- MIMasanori Ikeda
The University of Texas Medical Branch at Galveston, The University of Texas Southwestern Medical Center
Topics & keywords
- NS3
- NS2-3 protease
- Serine protease
- Interferon
- Viral replication
- Protease
- Hepatitis C virus
- Interferon regulatory factors
- Good health and well-being