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Modulation of interferon signaling by hepatitis C virus non-structural 5A protein: Implication of genotypic difference in interferon treatment
被引:7
|作者:
Kang, Sang-Min
[1
]
Won, Seung-Jae
[1
]
Lee, Gun-Hee
[1
]
Lim, Yun-Sook
[1
]
Hwang, Soon B.
[1
]
机构:
[1] Hallym Univ, Natl Res Lab Hepatitis C Virus, Ilsong Inst Life Sci, Anyang 431060, South Korea
关键词:
Hepatitis C virus;
NS5A protein;
Interferon signaling;
Differential interferon antagonism;
NECROSIS-FACTOR-ALPHA;
KAPPA-B;
EXPRESSION;
PATHWAY;
INTERLEUKIN-8;
KINASE;
INHIBITION;
INDUCTION;
TRANSDUCTION;
ACTIVATION;
D O I:
10.1016/j.febslet.2010.08.032
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Interferon (IFN) response rate in hepatitis C virus (HCV) patients has been varied with genotypes. In this study, we investigated the effects of HCV NS5A protein on IFN resistance and compared the genotypic differences of NS5A. We showed that IFN-alpha-, poly I:C-, and Sendai virus-induced ISRE transcriptional activities were inhibited by both genotype 1b and 2a NS5A protein. We demonstrated that not only genotype 1b but also genotype 2a NS5A exerted the similar extent of IFN-alpha-induced antiviral activity. We showed that NS5A derived from both genotype 1b and 2a showed no significant differential IFN responses as seen in HCV patients. These data imply that some other host factor may be involved in genotypic differences of IFN antagonism in HCV patients. (c) 2010 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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页码:4069 / 4076
页数:8
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