Control of cccDNA function in hepatitis B virus infection

被引:521
作者
Levrero, Massimo [1 ,2 ,3 ]
Pollicino, Teresa [4 ]
Petersen, Jorg [5 ]
Belloni, Laura [6 ]
Raimondo, Giovanni [4 ]
Dandri, Maura [7 ]
机构
[1] Univ Roma La Sapienza, Dept Internal Med, Policlin Umberto I, I-0061 Rome, Italy
[2] Regina Elena Inst Canc Res, Gene Express Lab, Andrea Cesalpino Fdn, Oncogenom Ctr, Rome, Italy
[3] Univ Roma La Sapienza, Gene Express Lab, Cenci Bolognetti Fdn, I-0061 Rome, Italy
[4] Univ Hosp Messina, Unit Clin & Mol Hepatol, Dept Internal Med, Messina, Italy
[5] Asclepius Klin S Georg, IFI Inst Interdisciplinary Med, Ctr Liver, Hamburg, Germany
[6] Univ Roma La Sapienza, Dept Gene Express, I-0061 Rome, Italy
[7] Univ Med Ctr Hamburg Eppendorf, Dept Internal Med, Hamburg, Germany
关键词
Hepatitis B virus; Covalently closed circular DNA; Chronic hepatitis B infection; cccDNA function; CLOSED CIRCULAR DNA; PLASMACYTOID DENDRITIC CELLS; LARGE ENVELOPE PROTEIN; CHRONIC HBV INFECTION; VIRAL-DNA; IN-VIVO; HEPATOCYTE TURNOVER; HEPADNAVIRUS INFECTIONS; EPIGENETIC REGULATION; CHROMATIN-STRUCTURE;
D O I
10.1016/j.jhep.2009.05.022
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The template of hepatitis B virus (HBV) transcription, the covalently closed circular DNA (cccDNA), plays a key role in the life cycle of the virus and permits the persistence of infection. Novel molecular techniques have opened new possibilities to investigate the organization and the activity of the cccDNA minichromosome in vivo, and recent advances have started to shed light on the complexity of the mechanisms controlling cccDNA function. Nuclear cccDNA accumulates in hepatocyte nuclei as a stable minichromosome organized by histone and non-histone viral and cellular proteins. Identification of the molecular mechanisms regulating cccDNA stability and its transcriptional activity at the RNA, DNA and epigenetic levels in the course of chronic hepatitis B (CH-B) infection may reveal new potential therapeutic targets for anti-HBV drugs and hence assist in the design of strategies aimed at silencing and eventually depleting the cccDNA reservoir., (C) 2009 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:581 / 592
页数:12
相关论文
共 89 条
  • [1] HBX binds in vivo on the HBV minichromosome, modifies the epigenetic regulation of ccc-DNA function and potentiates HBV replication
    Belloni, L.
    Poliicino, T.
    Cimino, L.
    Raffa, G.
    Raimondo, G.
    Levrero, M.
    [J]. JOURNAL OF HEPATOLOGY, 2008, 48 : S25 - S25
  • [2] MODULATION OF THE EPIGENETIC REGULATION OF CCCDNA FUNCTION CONTRIBUTES TO IFNα INHIBITION OF HBV REPLICATION
    Belloni, L.
    Testoni, B.
    Scisciani, C.
    Pollicino, T.
    Raimondo, G.
    Levrero, M.
    [J]. JOURNAL OF HEPATOLOGY, 2009, 50 : S32 - S33
  • [3] Structural organization of the hepatitis B virus minichromosome
    Bock, CT
    Schwinn, S
    Locarnini, S
    Fyfe, J
    Manns, MP
    Trautwein, C
    Zentgraf, H
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (01) : 183 - 196
  • [4] HEPATITIS-B VIRUS GENOME IS ORGANIZED INTO NUCLEOSOMES IN THE NUCLEUS OF THE INFECTED CELL
    BOCK, CT
    SCHRANZ, P
    SCHRODER, CH
    ZENTGRAF, H
    [J]. VIRUS GENES, 1994, 8 (03) : 215 - 229
  • [5] Characterization of hepatitis B virus (HBV)-specific T-cell dysfunction in chronic HBV infection
    Boni, Carolina
    Fisicaro, Paola
    Valdatta, Caterina
    Amadei, Barbara
    Di Vincenzo, Paola
    Giuberti, Tiziana
    Laccabue, Diletta
    Zerbini, Alessandro
    Cavalli, Albertina
    Missale, Gabriele
    Bertoletti, Antonio
    Ferrari, Carlo
    [J]. JOURNAL OF VIROLOGY, 2007, 81 (08) : 4215 - 4225
  • [6] Persistent hepatitis B virus infection in subjects without hepatitis B surface antigen:: Clinically significant or purely "occult"?
    Bréchot, C
    Thiers, V
    Kremsdorf, D
    Nalpas, B
    Pol, S
    Paterlini-Bréchot, P
    [J]. HEPATOLOGY, 2001, 34 (01) : 194 - 203
  • [7] Occult hepatitis B virus infection in chronic liver disease: Full-length genome and analysis of mutant surface promoter
    Chaudhuri, V
    Tayal, R
    Nayak, B
    Acharya, SK
    Panda, SK
    [J]. GASTROENTEROLOGY, 2004, 127 (05) : 1356 - 1371
  • [8] Activated plasmacytoid dendritic cells act synergistically with hepatitis B core antigen-pulsed monocyte-derived dendritic cells in the induction of hepatitis B virus-specific CD8 T-cell response
    Chen, Weiwei
    Zhang, Zheng
    Shi, Ming
    Chen, Liangen
    Fu, Junliang
    Shi, Feng
    Zhang, Bing
    Zhang, Hui
    Jin, Lei
    Wang, Fu-Sheng
    [J]. CLINICAL IMMUNOLOGY, 2008, 129 (02) : 295 - 303
  • [9] COUGOT D, 2007, 2007 INT M MOL BIOL
  • [10] Increased hepatocyte turnover and inhibition of woodchuck hepatitis B virus replication by adefovir in vitro do not lead to reduction of the closed circular DNA
    Dandri, M
    Burda, MR
    Will, H
    Petersen, J
    [J]. HEPATOLOGY, 2000, 32 (01) : 139 - 146