Cell entry of hepatitis C virus

被引:114
作者
Bartosch, B
Cosset, FL
机构
[1] Ecole Normale Super Lyon, INSERM, U758, F-69007 Lyon, France
[2] IFR128 BioSci Lyon Gerland, Lyon, France
关键词
hepatitis C virus; receptor; cell entry; glycoprotein; lipoprotein;
D O I
10.1016/j.virol.2005.12.027
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis C virus (HCV), an important human pathogen, is an enveloped, positive-stranded RNA virus classified in the hepacivirus genus of the Flaviviridae family. Cell attachment of flaviviruses generally leads to endocytosis of bound virions. Systems that support HCV replication and particle formation in vitro are emerging only now, 16 years after the discovery of the virus. Albeit this limitation, the route of HCV cell entry as well as 'capture' molecules involved in low-affinity interactions for the initial contact of HCV with target cells and potential high-affinity receptor candidates that may mediate HCV trafficking and fusion has been described. The objective of this review is to summarize the contribution of different HCV model systems to our Current knowledge about structure of the HCV GPs E1 and E2 and their roles in cell entry comprising cell attachment, interactions with cellular receptors, endocytosis, and fusion. (c) 2005 Elsevier Inc. All rights reserved.
引用
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页码:1 / 12
页数:12
相关论文
共 124 条
[51]   Incomplete humoral immunity against hepatitis C virus is linked with distinct recognition of putative multiple receptors by E2 envelope glycoprotein [J].
Heo, TH ;
Chang, JH ;
Lee, JW ;
Foung, SKH ;
Dubuisson, J ;
Kang, CY .
JOURNAL OF IMMUNOLOGY, 2004, 173 (01) :446-455
[52]   Identification of amino acid residues in CD81 critical for interaction with hepatitis C virus envelope glycoprotein E2 [J].
Higginbottom, A ;
Quinn, ER ;
Kuo, CC ;
Flint, M ;
Wilson, LH ;
Bianchi, E ;
Nicosia, A ;
Monk, PN ;
McKeating, JA ;
Levy, S .
JOURNAL OF VIROLOGY, 2000, 74 (08) :3642-3649
[53]   EQUILIBRIUM CENTRIFUGATION STUDIES OF HEPATITIS-C VIRUS - EVIDENCE FOR CIRCULATING IMMUNE-COMPLEXES [J].
HIJIKATA, M ;
SHIMIZU, YK ;
KATO, H ;
IWAMOTO, A ;
SHIH, JW ;
ALTER, HJ ;
PURCELL, RH ;
YOSHIKURA, H .
JOURNAL OF VIROLOGY, 1993, 67 (04) :1953-1958
[54]   Hepatitis C virus glycoproteins mediate pH-dependent cell entry of pseudotyped retroviral particles [J].
Hsu, M ;
Zhang, J ;
Flint, M ;
Logvinoff, C ;
Cheng-Mayer, C ;
Rice, CM ;
McKeating, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (12) :7271-7276
[55]  
KANTO T, 1994, HEPATOLOGY, V19, P296
[56]   Sequence analysis of hepatitis C virus isolated from a fulminant hepatitis patient [J].
Kato, T ;
Furusaka, A ;
Miyamoto, M ;
Date, T ;
Yasui, K ;
Hiramoto, J ;
Nagayama, K ;
Tanaka, T ;
Wakita, T .
JOURNAL OF MEDICAL VIROLOGY, 2001, 64 (03) :334-339
[57]   Hepatitis C virus E2 has three immunogenic domains containing conformational epitopes with distinct properties and biological functions [J].
Keck, ZY ;
Op de Beeck, A ;
Hadlock, KG ;
Xia, JM ;
Li, TK ;
Dubuisson, J ;
Foung, SKH .
JOURNAL OF VIROLOGY, 2004, 78 (17) :9224-9232
[58]  
KOUTSOUDAKIS G, COMMUNICATION
[59]   Structure of dengue virus: Implications for flavivirus organization, maturation, and fusion [J].
Kuhn, RJ ;
Zhang, W ;
Rossmann, MG ;
Pletnev, SV ;
Corver, J ;
Lenches, E ;
Jones, CT ;
Mukhopadhyay, S ;
Chipman, PR ;
Strauss, EG ;
Baker, TS ;
Strauss, JH .
CELL, 2002, 108 (05) :717-725
[60]   Functional role of hepatitis C virus chimeric glycoproteins in the infectivity of pseudotyped virus [J].
Lagging, LM ;
Meyer, K ;
Owens, RJ ;
Ray, R .
JOURNAL OF VIROLOGY, 1998, 72 (05) :3539-3546