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Early steps of the hepatitis C virus life cycle
被引:95
作者:

Dubuisson, Jean
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机构:
Univ Lille 1, CNRS, Inst Biol Lille, UMR8161, Lille, France Univ Lille 1, CNRS, Inst Biol Lille, UMR8161, Lille, France

Helle, Francois
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机构: Univ Lille 1, CNRS, Inst Biol Lille, UMR8161, Lille, France

Cocquerel, Laurence
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机构: Univ Lille 1, CNRS, Inst Biol Lille, UMR8161, Lille, France
机构:
[1] Univ Lille 1, CNRS, Inst Biol Lille, UMR8161, Lille, France
关键词:
D O I:
10.1111/j.1462-5822.2007.01107.x
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
To replicate its genome, a virus needs to cross the plasma membrane of a host cell and get access to cytosolic and/or nuclear components. For an enveloped virus, this involves binding to the plasma membrane, followed by migration of the virion to a microdomain or an endosomal vesicle where fusion between the virion envelope and a host cell membrane occurs. Increasing evidences indicate that virus entry is a tightly regulated process. Although we are still far from understanding the details of hepatitis C virus (HCV) entry, recent data show that this virus enters into target cells in a slow and complex multistep process involving the presence of several entry factors. Initial attachment of the virion may involve glycosaminoglycans and the low-density lipoprotein receptor, and it is followed by the sequential interaction with the scavenger receptor class B type I, the tetraspanin CD81 and tight junction protein Claudin-1, -6 or -9. Furthermore, the identification of EWI-2wint as a new partner of CD81 which blocks E2-CD81 interaction provides additional evidence of the complexity of the HCV entry process. The current knowledge accumulated on HCV entry is summarized in this review.
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页码:821 / 827
页数:7
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