The HepaRG cell line: a valuable in vitro tool for hepatitis virus infection studies

被引:0
作者
Liesbeth Ceelen
Marusya Lieveld
Ramses Forsyth
Mathieu Vinken
机构
[1] Pathlicon,Department of Toxicology, Faculty of Medicine and Pharmacy
[2] Center for Pharmaceutical Research,undefined
来源
Hepatology International | 2013年 / 7卷
关键词
HepaRG cell line; In vitro model; Hepatitis B virus; Hepatitis C virus; Viral entry;
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学科分类号
摘要
Hepatitis virus infections, mainly hepatitis B virus (HBV) and hepatitis C virus (HCV) infections, constitute a major problem for public health since they have a worldwide distribution and because they are associated with hepatocellular carcinoma and death. Current anti-HBV vaccines seem to be effective in the majority of people. However, an important issue waiting to be tackled nowadays is how to cure patients with chronic hepatitis B. Moreover, no vaccine is available today for the prevention of HCV infection. Therefore, the use of adequate in vitro infection systems is a prerequisite for the molecular understanding of the infection events of these viruses, which could result in the development of novel powerful therapeutics. In this respect, the HepaRG cell line exhibits a hepatocyte-like morphology and displays drug metabolism capacity similar to that of primary hepatocytes. HepaRG cells have yet been proven to be a useful tool in the study of viral infections, particularly for deciphering the mechanism of HBV entry into hepatocytes.
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页码:394 / 399
页数:5
相关论文
共 180 条
[51]  
Lütgehetmann M(2010)Hepatitis B virus requires intact caveolin-1 function for productive infection in HepaRG cells J Virol 84 243-131
[52]  
Petersen J(2007)Hepatitis B virus infection initiates with a large surface protein-dependent binding to heparan sulfate proteoglycans Hepatology 46 1759-10466
[53]  
Dandri M(1998)Dynamin and its partners: a progress report Curr Opin Cell Biol 10 504-13066
[54]  
Lutgehetmann M(2006)The role of the HBV envelope proteins in the HDV replication cycle Curr Top Microbiol Immunol 307 113-760
[55]  
Volz T(2005)Role of the antigenic loop of the hepatitis B virus envelope proteins in infectivity of hepatitis delta virus J Virol 79 10460-1275
[56]  
Petersen J(2007)Entry of hepatitis delta virus requires the conserved cysteine residues of the hepatitis B virus envelope protein antigenic loop and is blocked by inhibitors of thiol-disulfide exchange J Virol 81 13057-322
[57]  
Zoulim F(2006)Characterization of a hepatitis B and hepatitis delta virus receptor binding site Hepatology 43 750-60
[58]  
Tariq H(2012)Decreased infectivity of nucleoside analogs-resistant hepatitis B virus mutants J Hepatol 56 1269-1003
[59]  
Manzoor S(2001)Kinetics of hepadnavirus loss from the liver during inhibition of viral DNA synthesis J Virol 75 311-8918
[60]  
Parvaiz F(2010)Development of cell cultures that express hepatitis B virus to high levels and accumulate cccDNA J Virol Methods 169 52-1716