論文

査読有り
2006年3月

Anti-viral protein APOBEC3G is induced by interferon-alpha stimulation in human hepatocytes

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
  • Y Tanaka
  • H Marusawa
  • H Seno
  • Y Matsumoto
  • Y Ueda
  • Y Kodama
  • Y Endo
  • J Yamauchi
  • T Matsumoto
  • A Takaori-Kondo
  • Ikai, I
  • T Chiba
  • 全て表示

341
2
開始ページ
314
終了ページ
319
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1016/j.bbrc.2005.12.192
出版者・発行元
ACADEMIC PRESS INC ELSEVIER SCIENCE

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.

リンク情報
DOI
https://doi.org/10.1016/j.bbrc.2005.12.192
J-GLOBAL
https://jglobal.jst.go.jp/detail?JGLOBAL_ID=200902229272852412
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/16426578
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000235414400007&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.bbrc.2005.12.192
  • ISSN : 0006-291X
  • J-Global ID : 200902229272852412
  • PubMed ID : 16426578
  • Web of Science ID : WOS:000235414400007

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