CD81 is required for hepatitis C virus glycoprotein-mediated viral infection

被引:284
作者
Zhang, J
Randall, G
Higginbottom, A
Monk, P
Rice, CM
McKeating, JA
机构
[1] Rockefeller Univ, Ctr Study Hepatitis C, Lab Virol & Infect Dis, New York, NY 10021 USA
[2] Univ Sheffield, Sch Med & Biomed Sci, Sheffield S10 2RX, S Yorkshire, England
关键词
D O I
10.1128/JVI.78.3.1448-1455.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
CD81 has been described as a putative receptor for hepatitis C virus (HCV); however, its role in HCV cell entry has not been characterized due to the lack of an efficient cell culture system. We have examined the role of CD81 in HCV glycoprotein-dependent entry by using a recently developed retroviral pseudotyping system. Human immunodeficiency virus (HIV) pseudotypes bearing HCV E1E2 glycoproteins show a restricted tropism for human liver cell lines. Although all of the permissive cell lines express CD81, CD81 expression alone is not sufficient to allow viral entry. CD81 is required for HIV-HCV pseudotype infection since (i) a monoclonal antibody specific for CD81 inhibited infection of susceptible target cells and (ii) silencing of CD81 expression in Huh-7.5 hepatoma cells by small interfering RNAs inhibited HIV-HCV pseudotype infection. Furthermore, expression of CD81 in human liver cells that were previously resistant to infection, HepG2 and HH29, conferred permissivity of HCV pseudotype infection. The characterization of chimeric CD9/CD81 molecules confirmed that the large extracellular loop of CD81 is a determinant for viral entry. These data suggest a functional role for CD81 as a coreceptor for HCV glycoprotein-dependent viral cell entry.
引用
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页码:1448 / 1455
页数:8
相关论文
共 46 条
[1]   Hepatitis C virus and other Flaviviridae viruses enter cells via low density lipoprotein receptor [J].
Agnello, V ;
Abel, G ;
Elfahal, M ;
Knight, GB ;
Zhang, QX .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (22) :12766-12771
[2]   Hepatitis C virus envelope protein E2 binds to CD81 of tamarins [J].
Allander, T ;
Forns, X ;
Emerson, SU ;
Purcell, RH ;
Bukh, J .
VIROLOGY, 2000, 277 (02) :358-367
[3]   Infectious hepatitis C virus pseudo-particles containing functional E1-E2 envelope protein complexes [J].
Bartosch, B ;
Dubuisson, J ;
Cosset, FL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2003, 197 (05) :633-642
[4]   Hepatitis C virus structural proteins assemble into viruslike particles in insect cells [J].
Baumert, TF ;
Ito, S ;
Wong, DT ;
Liang, TJ .
JOURNAL OF VIROLOGY, 1998, 72 (05) :3827-3836
[5]   Highly permissive cell lines for subgenomic and genomic hepatitis C virus RNA replication [J].
Blight, KJ ;
McKeating, JA ;
Rice, CM .
JOURNAL OF VIROLOGY, 2002, 76 (24) :13001-13014
[6]   Characterization of vesicular stomatitis virus recombinants that express and incorporate high levels of hepatitis C virus glycoproteins [J].
Buonocore, L ;
Blight, KJ ;
Rice, CM ;
Rose, JK .
JOURNAL OF VIROLOGY, 2002, 76 (14) :6865-6872
[7]   Alpha interferon inhibits hepatitis C virus replication in primary human hepatocytes infected in vitro [J].
Castet, V ;
Fournier, C ;
Soulier, A ;
Brillet, R ;
Coste, J ;
Larrey, D ;
Dhumeaux, D ;
Maurel, P ;
Pawlotsky, JM .
JOURNAL OF VIROLOGY, 2002, 76 (16) :8189-8199
[8]   Evaluation of prototype transmembrane 4 superfamily protein complexes and their relation to lipid rafts [J].
Claas, C ;
Stipp, CS ;
Hemler, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (11) :7974-7984
[9]   VPR IS REQUIRED FOR EFFICIENT REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 IN MONONUCLEAR PHAGOCYTES [J].
CONNOR, RI ;
CHEN, BK ;
CHOE, S ;
LANDAU, NR .
VIROLOGY, 1995, 206 (02) :935-944
[10]  
Flint K, 1999, LE EXPLORAT LIT CUL, V2, P81