Title

Impaired expression and function of toll-like receptor 7 in hepatitis C virus infection in human hepatoma cells

UMMS Affiliation

Department of Medicine, Division of Gastroenterology

Publication Date

1-2010

Document Type

Article

Subjects

Carcinoma, Hepatocellular; Cell Line, Tumor; Hepacivirus; Hepatitis C; Humans; Interferon Regulatory Factor-7; Interferon-alpha; Liver Neoplasms; RNA, Messenger; Toll-Like Receptor 7; Up-Regulation

Disciplines

Gastroenterology

Abstract

Hepatitis C virus (HCV) interferes with interferon (IFN)-mediated innate immune defenses. Toll-like receptor (TLR) 7 agonists robustly inhibit HCV infection. We hypothesize that HCV infection may interfere with the expression and/or function of TLR7, a sensor of single-stranded RNA. We identified reduced TLR7 RNA and protein levels in hepatoma cells expressing HCV (full-length, BB7-subgenomic, and JFH-1 clone) compared with control HCV-naive cells. The biological relevance of this finding was confirmed by the observation of decreased TLR7 RNA in livers of HCV-infected patients compared with controls. HCV clearance, by IFN-alpha treatment or restrictive culture conditions, restored the decreased TLR7 expression. Treatment with RNA polymerase inhibitors revealed a shorter TLR7 half-life in HCV-replicating cells compared with controls. Downstream of TLR7, an increased baseline IRF7 nuclear translocation was observed in HCV-positive cells compared with controls. Stimulation with the TLR7 ligand R837 resulted in significant IRF7 nuclear translocation in control cells. In contrast, HCV-replicating cells showed attenuated TLR7 ligand-induced IRF7 activation. CONCLUSION: Reduced TLR7 expression, due to RNA instability, directly correlates with HCV replication and alters TLR7-induced IRF7-mediated cell activation. These results suggest a role for TLR7 in HCV-mediated evasion of host immune surveillance.

DOI of Published Version

10.1002/hep.23256

Source

Hepatology. 2010 Jan;51(1):35-42. Link to article on publisher's site

Journal/Book/Conference Title

Hepatology (Baltimore, Md.)

Related Resources

Link to Article in PubMed

PubMed ID

19821521

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