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Anti-viral protein APOBEC3G is induced by interferon-α stimulation in human hepatocytes
被引:127
作者:
Tanaka, Y
Marusawa, H
Seno, H
Matsumoto, Y
Ueda, Y
Kodama, Y
Endo, Y
Yamauchi, J
Matsumoto, T
Takaori-Kondo, A
Ikai, I
Chiba, T
[1
]
机构:
[1] Kyoto Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Hematol & Oncol, Kyoto 6068507, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Surg Gastroenterol, Kyoto 6068507, Japan
基金:
日本学术振兴会;
关键词:
APOBEC3G;
interferon-alpha;
hepatocytes;
D O I:
10.1016/j.bbrc.2005.12.192
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:
Apolipoprotein B mRNA-editing enzyme catalytic-polypeptide 3G (APOBEC3G) is a potent inhibitor of infection by a wide range of retroviruses. Although recent reports have suggested that human APOBEC3G exerts antiviral activity against hepatitis B virus, APOBEC3G expression is normally low in the human liver. To clarify the role of APOBEOG in cellular defenses against hepatitis Viruses, the regulation of the APOBEOG expression was investigated in human hepatocytes. Endogenous transcripts of nine APOBEC family members were barely detectable in quiescent liver cells. However, APOBEC3G was significantly up-regulated in response to interferon-alpha (IFN-alpha) stimulation in HepG2 Huh-7, and primary human hepatocytcs. IFN regulatory factor elements that are important for IFN-inducible promoter activity were identified 5' upstream from the human APOBEC3G gene. Our findings provided the first evidence showing that APOBEOG is induced by IFN stimulation in human hepatocytes and thus could be involved in host defense mechanisms directed against hepatitis Viruses. (c) 2006 Elsevier Inc. All rights reserved.
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页码:314 / 319
页数:6
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