Author: Mizui, Tomokazu; Yamashina, Shunhei; Tanida, Isei; Takei, Yoshiyuki; Ueno, Takashi; Sakamoto, Naoya; Ikejima, Kenichi; Kitamura, Tsuneo; Enomoto, Nobuyuki; Sakai, Tatsuo; Kominami, Eiki; Watanabe, Sumio
Title: Inhibition of hepatitis C virus replication by chloroquine targeting virus-associated autophagy Cord-id: qw1ig2v4 Document date: 2009_9_17
ID: qw1ig2v4
Snippet: BACKGROUND: Autophagy has been reported to play a pivotal role on the replication of various RNA viruses. In this study, we investigated the role of autophagy on hepatitis C virus (HCV) RNA replication and demonstrated anti-HCV effects of an autophagic proteolysis inhibitor, chloroquine. METHODS: Induction of autophagy was evaluated following the transfection of HCV replicon to Huh-7 cells. Next, we investigated the replication of HCV subgenomic replicon in response to treatment with lysosomal p
Document: BACKGROUND: Autophagy has been reported to play a pivotal role on the replication of various RNA viruses. In this study, we investigated the role of autophagy on hepatitis C virus (HCV) RNA replication and demonstrated anti-HCV effects of an autophagic proteolysis inhibitor, chloroquine. METHODS: Induction of autophagy was evaluated following the transfection of HCV replicon to Huh-7 cells. Next, we investigated the replication of HCV subgenomic replicon in response to treatment with lysosomal protease inhibitors or pharmacological autophagy inhibitor. The effect on HCV replication was analyzed after transfection with siRNA of ATG5, ATG7 and light-chain (LC)-3 to replicon cells. The antiviral effect of chloroquine and/or interferon-α (IFNα) was evaluated. RESULTS: The transfection of HCV replicon increased the number of autophagosomes to about twofold over untransfected cells. Pharmacological inhibition of autophagic proteolysis significantly suppressed expression level of HCV replicon. Silencing of autophagy-related genes by siRNA transfection significantly blunted the replication of HCV replicon. Treatment of replicon cells with chloroquine suppressed the replication of the HCV replicon in a dose-dependent manner. Furthermore, combination treatment of chloroquine to IFNα enhanced the antiviral effect of IFNα and prevented re-propagation of HCV replicon. Protein kinase R was activated in cells treated with IFNα but not with chloroquine. Incubation with chloroquine decreased degradation of long-lived protein leucine. CONCLUSION: The results of this study suggest that the replication of HCV replicon utilizes machinery involving cellular autophagic proteolysis. The therapy targeted to autophagic proteolysis by using chloroquine may provide a new therapeutic option against chronic hepatitis C.
Search related documents:
Co phrase search for related documents- absence presence and long term treatment: 1, 2
- absence presence and louis sigma: 1, 2
- absence presence and luciferase activity: 1, 2, 3, 4, 5
- absence presence and luciferase assay: 1
- absence presence and lysosomal function: 1
- liver disease and long term treatment: 1, 2, 3, 4, 5, 6, 7
- liver disease and luciferase activity: 1
- liver disease and luciferase assay: 1
Co phrase search for related documents, hyperlinks ordered by date