中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Productive hbv infection of well-differentiated, hntcp-expressing human hepatoma-derived (huh7) cells

文献类型:期刊论文

作者Zhou, Ming1,2,3; Zhao, Kaitao1; Yao, Yongxuan1; Yuan, Yifei1; Pei, Rongjuan1; Wang, Yun1; Chen, Jizheng1; Hu, Xue1; Zhou, Yuan1; Chen, Xinwen1
刊名Virologica sinica
出版日期2017-12-01
卷号32期号:6页码:465-475
关键词Hepatitis b virus (hbv) Na plus /taurocholate cotransporting polypeptide (ntcp) Huh7 Dimethyl sulfoxide (dmso) Polyethylene glycol (peg) Susceptibility
ISSN号1674-0769
DOI10.1007/s12250-017-3983-x
通讯作者Wu, chunchen(wucc@wh.iov.cn)
英文摘要Feasible and effective cell models for hepatitis b virus (hbv) infection are required for investigating the complete lifecycle of this virus, including the early steps of viral entry. resistance to dimethyl sulfoxide/polyethylene glycol (dmso/peg), hntcp expression, and a differentiated state are the limiting factors for successful hbv infection models. in the present study, we used a hepatoma cell line (huh7d(hntcp)) to overcome these limiting factors so that it exhibits excellent susceptibility to hbv infection. to achieve this goal, different hepatoma cell lines were tested with 2.5% dmso / 4% peg8000, and one resistant cell line (huh7d) was used to construct a stable hntcp-expressing cell line (huh7d(hntcp)) using a recombinant lentivirus system. then, the morphological characteristics and differentiation molecular markers of huh7d(hntcp) cells with or without dmso treatment were characterized. finally, the susceptibility of huh7d(hntcp) cells to hbv infection was assessed. our results showed that huh7d cells were resistant to 2.5% dmso / 4% peg8000, whereas the others were not. huh7d(hntcp) cells were established to express a high level of hntcp compared to liver extracts, and huh7d(hntcp) cells rapidly transformed into a non-dividing, well-differentiated polarized phenotype under dmso treatment. huh7d(hntcp) cells fully supported the entire lifecycle of hbv infection. this cell culture system will be useful for the analysis of host-virus interactions, which should facilitate the discovery of antiviral drugs and vaccines.
WOS关键词HEPATITIS-B-VIRUS ; PRIMARY TUPAIA HEPATOCYTES ; ADULT HUMAN HEPATOCYTES ; HUMAN FETAL HEPATOCYTES ; C-VIRUS ; REPLICATION ; ENTRY ; LINES ; POLARIZATION ; VECTOR
WOS研究方向Virology
WOS类目Virology
语种英语
WOS记录号WOS:000419186700003
出版者SPRINGER
URI标识http://www.irgrid.ac.cn/handle/1471x/2373343
专题武汉病毒研究所
通讯作者Wu, Chunchen
作者单位1.Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Hubei, Peoples R China
2.Shenzhen Univ, State & Local Joint Canc Genome Clin Applicat Key, Shenzhen Xenotransplantat Res & Dev Ctr, Shenzhen Peoples Hosp 2,Affiliated Hosp 1, Shenzhen 518035, Peoples R China
3.Sun Yat Sen Univ, Inst Immunol, Zhongshan Sch Med, Guangdong Prov Key Lab Organ Donat & Transplant I, Guangzhou 510080, Guangdong, Peoples R China
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GB/T 7714
Zhou, Ming,Zhao, Kaitao,Yao, Yongxuan,et al. Productive hbv infection of well-differentiated, hntcp-expressing human hepatoma-derived (huh7) cells[J]. Virologica sinica,2017,32(6):465-475.
APA Zhou, Ming.,Zhao, Kaitao.,Yao, Yongxuan.,Yuan, Yifei.,Pei, Rongjuan.,...&Wu, Chunchen.(2017).Productive hbv infection of well-differentiated, hntcp-expressing human hepatoma-derived (huh7) cells.Virologica sinica,32(6),465-475.
MLA Zhou, Ming,et al."Productive hbv infection of well-differentiated, hntcp-expressing human hepatoma-derived (huh7) cells".Virologica sinica 32.6(2017):465-475.

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来源:武汉病毒研究所

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