Inducible expression of human hepatitis B virus (HBV) in stably transfected hepatoblastoma cells: A novel system for screening potential inhibitors of HBV replication

被引:534
作者
Ladner, SK
Otto, MJ
Barker, CS
Zaifert, K
Wang, GH
Guo, JT
Seeger, C
King, RW
机构
[1] AVID THERAPEUT INC,PHILADELPHIA,PA 19104
[2] FOX CHASE CANC CTR,INST CANC RES,PHILADELPHIA,PA 19111
关键词
D O I
10.1128/AAC.41.8.1715
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We report the development and isolation of a cell line, termed HepAD38, that replicates human hepatitis B virus (HBV) under conditions that can be regulated with tetracycline. In the presence of the antibiotic, this cell line is free of virus due to the repression of pregenomic (pg) RNA synthesis, Upon removal of tetracycline from the culture medium, the cells express viral pg RNA, accumulate subviral particles in the cytoplasm that contain DNA intermediates characteristic of viral replication, and secrete virus-like particles Into the supernatant. Since the HepAD38 cell line can produce high levels of HBV DNA, it should be useful for analyses of the viral replication cycle that depend upon viral DNA synthesis in a synchronized fashion, In addition, this cell line has been formatted into a high-throughput, cell-based assay that permits the large-scale screening of diverse compound libraries for new classes of inhibitors of HBV replication.
引用
收藏
页码:1715 / 1720
页数:6
相关论文
共 34 条
[1]   HEPATITIS-B VIRUS PRODUCED BY TRANSFECTED HEP G2 CELLS CAUSES HEPATITIS IN CHIMPANZEES [J].
ACS, G ;
SELLS, MA ;
PURCELL, RH ;
PRICE, P ;
ENGLE, R ;
SHAPIRO, M ;
POPPER, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (13) :4641-4644
[2]  
Beasley R.P., 1984, VIRAL HEPATITIS LIVE, P209
[3]   AMPLIFICATION OF EXPRESSION OF HEPATITIS-B SURFACE-ANTIGEN IN 3T3 CELLS COTRANSFECTED WITH A DOMINANT-ACTING GENE AND CLONED VIRAL-DNA [J].
CHRISTMAN, JK ;
GERBER, M ;
PRICE, PM ;
FLORDELLIS, C ;
EDELMAN, J ;
ACS, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (06) :1815-1819
[4]   TRANSACTIVATION OF HUMAN-IMMUNODEFICIENCY-VIRUS OCCURS VIA A BIMODAL MECHANISM [J].
CULLEN, BR .
CELL, 1986, 46 (07) :973-982
[5]   INHIBITION OF HEPATITIS-B VIRUS IN TISSUE-CULTURE BY ALPHA-INTERFERON [J].
DAVIS, MG ;
JANSEN, RW .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1994, 38 (12) :2921-2924
[6]  
DEINSTAG JI, 1995, NEW ENGL J MED, V333, P1657
[7]   MUTATIONS IN THE EPSILON-SEQUENCES OF HUMAN HEPATITIS-B VIRUS AFFECT BOTH RNA ENCAPSIDATION AND REVERSE TRANSCRIPTION [J].
FALLOWS, DA ;
GOFF, SP .
JOURNAL OF VIROLOGY, 1995, 69 (05) :3067-3073
[8]   LONG-TERM FOLLOW-UP OF ANTI-HBE-POSITIVE CHRONIC ACTIVE HEPATITIS-B [J].
FATTOVICH, G ;
BROLLO, L ;
ALBERTI, A ;
PONTISSO, P ;
GIUSTINA, G ;
REALDI, G .
HEPATOLOGY, 1988, 8 (06) :1651-1654
[9]   THE EFFECT OF ABSOLUTE-CONFIGURATION ON THE ANTI-HIV AND ANTI-HBV ACTIVITY OF NUCLEOSIDE ANALOGS [J].
FURMAN, PA ;
WILSON, JE ;
REARDON, JE ;
PAINTER, GR .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1995, 6 (06) :345-355
[10]   THE MOLECULAR-BIOLOGY OF THE HEPATITIS-B VIRUSES [J].
GANEM, D ;
VARMUS, HE .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :651-693