• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Production of infectious hepatitis C virus by well-differentiated, growth-arrested human hepatoma-derived cells.高分化、生长停滞的人肝癌衍生细胞产生传染性丙型肝炎病毒。
J Virol. 2006 Oct;80(20):10253-7. doi: 10.1128/JVI.01059-06.
2
Human serum leads to differentiation of human hepatoma cells, restoration of very-low-density lipoprotein secretion, and a 1000-fold increase in HCV Japanese fulminant hepatitis type 1 titers.人血清可诱导人肝癌细胞分化,恢复极低密度脂蛋白分泌,并使 HCV 日本暴发性肝炎 1 型滴度增加 1000 倍。
Hepatology. 2013 Dec;58(6):1907-17. doi: 10.1002/hep.26566. Epub 2013 Oct 17.
3
Low perforin expression of early differentiated HCV-specific CD8+ T cells limits their hepatotoxic potential.早期分化的 HCV 特异性 CD8+T 细胞中穿孔素表达水平低,限制了其肝毒性潜能。
J Hepatol. 2012 Jul;57(1):9-16. doi: 10.1016/j.jhep.2012.02.030. Epub 2012 Mar 14.
4
Production of infectious hepatitis C virus in primary cultures of human adult hepatocytes.在原代培养的成人人类肝细胞中生产传染性丙型肝炎病毒。
Gastroenterology. 2010 Oct;139(4):1355-64. doi: 10.1053/j.gastro.2010.06.058. Epub 2010 Jul 1.
5
Hepatitis C virus triggers apoptosis of a newly developed hepatoma cell line through antiviral defense system.丙型肝炎病毒通过抗病毒防御系统触发新建立的肝癌细胞系的凋亡。
Gastroenterology. 2007 Nov;133(5):1649-59. doi: 10.1053/j.gastro.2007.09.017. Epub 2007 Sep 16.
6
Primary hepatocyte culture supports hepatitis C virus replication: a model for infection-associated hepatocarcinogenesis.原代肝细胞培养支持丙型肝炎病毒复制:感染相关肝癌发生的模型。
Hepatology. 2010 Jun;51(6):1922-32. doi: 10.1002/hep.23616.
7
Establishment of persistent hepatitis C virus infection and replication in vitro.丙型肝炎病毒体外持续感染与复制的建立。
J Gen Virol. 1997 Oct;78 ( Pt 10):2467-76. doi: 10.1099/0022-1317-78-10-2467.
8
Identification of host genes showing differential expression profiles with cell-based long-term replication of hepatitis C virus RNA.鉴定具有丙型肝炎病毒 RNA 基于细胞的长期复制的差异表达谱的宿主基因。
Virus Res. 2012 Jul;167(1):74-85. doi: 10.1016/j.virusres.2012.04.008. Epub 2012 May 1.
9
Infection of a human hepatoma cell line by hepatitis B virus.乙型肝炎病毒对人肝癌细胞系的感染。
Proc Natl Acad Sci U S A. 2002 Nov 26;99(24):15655-60. doi: 10.1073/pnas.232137699. Epub 2002 Nov 13.
10
Efficient replication systems for hepatitis C virus using a new human hepatoma cell line.利用新型人肝癌细胞系建立丙型肝炎病毒高效复制系统。
Virus Res. 2009 Dec;146(1-2):41-50. doi: 10.1016/j.virusres.2009.08.006. Epub 2009 Aug 29.

引用本文的文献

1
A novel system for simultaneous infections with hepatitis B, C, D and E viruses.一种用于同时感染乙肝、丙肝、丁肝和戊肝病毒的新型系统。
JHEP Rep. 2025 Feb 28;7(5):101383. doi: 10.1016/j.jhepr.2025.101383. eCollection 2025 May.
2
Cytoskeletal Vimentin Directs Cell-Cell Transmission of Hepatitis C Virus.细胞骨架波形蛋白指导丙型肝炎病毒的细胞间传播。
Adv Sci (Weinh). 2025 Jan;12(3):e2408917. doi: 10.1002/advs.202408917. Epub 2024 Nov 29.
3
Rapid Rescue of Goose Astrovirus Genome via Red/ET Assembly.通过 Red/ET 组装快速拯救鹅星状病毒基因组。
Food Environ Virol. 2024 Sep;16(3):297-306. doi: 10.1007/s12560-024-09593-4. Epub 2024 Apr 6.
4
A Multifaceted Approach for Evaluating Hepatitis E Virus Infectivity In Vitro: Cell Culture and Innovative Molecular Methods for Integrity Assessment.一种体外评估戊型肝炎病毒感染性的多方面方法:细胞培养及用于完整性评估的创新分子方法
Vet Sci. 2023 Nov 27;10(12):676. doi: 10.3390/vetsci10120676.
5
Role of hepcidin upregulation and proteolytic cleavage of ferroportin 1 in hepatitis C virus-induced iron accumulation.丙型肝炎病毒诱导的铁蓄积中铁调素上调和铁蛋白 1 蛋白水解切割的作用。
PLoS Pathog. 2023 Aug 16;19(8):e1011591. doi: 10.1371/journal.ppat.1011591. eCollection 2023 Aug.
6
Regulatory Role of Ribonucleotide Reductase Subunit M2 in Hepatocyte Growth and Pathogenesis of Hepatitis C Virus.核苷酸还原酶亚单位 M2 在肝细胞生长和丙型肝炎病毒发病机制中的调控作用。
Int J Mol Sci. 2023 Jan 30;24(3):2619. doi: 10.3390/ijms24032619.
7
The Rationality of Implementation of Dimethyl Sulfoxide as Differentiation-inducing Agent in Cancer Therapy.二甲基亚砜作为癌症治疗中分化诱导剂应用的合理性
Cancer Diagn Progn. 2023 Jan 3;3(1):1-8. doi: 10.21873/cdp.10172. eCollection 2023 Jan-Feb.
8
Transcriptional and Epigenetic Consequences of DMSO Treatment on HepaRG Cells.DMSO 处理对 HepaRG 细胞的转录和表观遗传后果。
Cells. 2022 Jul 26;11(15):2298. doi: 10.3390/cells11152298.
9
NS5A-ISGylation via Lysine 26 Has a Critical Role for Efficient Propagation of Hepatitis C Virus Genotype 2a.NS5A-ISGylation 通过赖氨酸 26 对丙型肝炎病毒基因型 2a 的有效复制起关键作用。
Kobe J Med Sci. 2021 Sep 30;67(2):E38-E47.
10
A human liver cell-based system modeling a clinical prognostic liver signature for therapeutic discovery.基于人源肝细胞的系统,用于对临床预后相关肝脏标志物进行建模,以发现治疗药物。
Nat Commun. 2021 Sep 17;12(1):5525. doi: 10.1038/s41467-021-25468-9.

本文引用的文献

1
Generation of infectious hepatitis C virus in immortalized human hepatocytes.在永生化人肝细胞中产生传染性丙型肝炎病毒。
J Virol. 2006 May;80(9):4633-9. doi: 10.1128/JVI.80.9.4633-4639.2006.
2
Multistable and multistep dynamics in neutrophil differentiation.中性粒细胞分化中的多稳态和多步动力学
BMC Cell Biol. 2006 Feb 28;7:11. doi: 10.1186/1471-2121-7-11.
3
Production of infectious genotype 1a hepatitis C virus (Hutchinson strain) in cultured human hepatoma cells.在培养的人肝癌细胞中产生具有传染性的1a基因型丙型肝炎病毒(哈钦森毒株)。
Proc Natl Acad Sci U S A. 2006 Feb 14;103(7):2310-5. doi: 10.1073/pnas.0510727103. Epub 2006 Feb 6.
4
Effect of cell growth on hepatitis C virus (HCV) replication and a mechanism of cell confluence-based inhibition of HCV RNA and protein expression.细胞生长对丙型肝炎病毒(HCV)复制的影响以及基于细胞汇合抑制HCV RNA和蛋白质表达的机制。
J Virol. 2006 Feb;80(3):1181-90. doi: 10.1128/JVI.80.3.1181-1190.2006.
5
Dimethyl sulfoxide as an inducer of differentiation in preosteoblast MC3T3-E1 cells.二甲基亚砜作为前成骨细胞MC3T3-E1细胞分化的诱导剂。
FEBS Lett. 2006 Jan 9;580(1):121-6. doi: 10.1016/j.febslet.2005.11.062. Epub 2005 Dec 6.
6
Dissecting the interferon-induced inhibition of hepatitis C virus replication by using a novel host cell line.利用一种新型宿主细胞系剖析干扰素诱导的丙型肝炎病毒复制抑制作用。
J Virol. 2005 Nov;79(21):13778-93. doi: 10.1128/JVI.79.21.13778-13793.2005.
7
Expression of cytochromes P450, conjugating enzymes and nuclear receptors in human hepatoma HepaRG cells.细胞色素P450、结合酶和核受体在人肝癌HepaRG细胞中的表达
Drug Metab Dispos. 2006 Jan;34(1):75-83. doi: 10.1124/dmd.105.006759. Epub 2005 Oct 4.
8
Stealth and cunning: hepatitis B and hepatitis C viruses.隐匿与狡黠:乙型肝炎病毒和丙型肝炎病毒
J Virol. 2005 Aug;79(15):9369-80. doi: 10.1128/JVI.79.15.9369-9380.2005.
9
Production of infectious hepatitis C virus in tissue culture from a cloned viral genome.从克隆的病毒基因组在组织培养中产生传染性丙型肝炎病毒。
Nat Med. 2005 Jul;11(7):791-6. doi: 10.1038/nm1268. Epub 2005 Jun 12.
10
Complete replication of hepatitis C virus in cell culture.丙型肝炎病毒在细胞培养中的完全复制。
Science. 2005 Jul 22;309(5734):623-6. doi: 10.1126/science.1114016. Epub 2005 Jun 9.

高分化、生长停滞的人肝癌衍生细胞产生传染性丙型肝炎病毒。

Production of infectious hepatitis C virus by well-differentiated, growth-arrested human hepatoma-derived cells.

作者信息

Sainz Bruno, Chisari Francis V

机构信息

Department of Molecular and Experimental Medicine, The Scripps Research Institute, 10550 North Torrey Pines Road, SBR-10, La Jolla, CA 92037, USA.

出版信息

J Virol. 2006 Oct;80(20):10253-7. doi: 10.1128/JVI.01059-06.

DOI:10.1128/JVI.01059-06
PMID:17005703
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1617281/
Abstract

Dimethyl sulfoxide (DMSO) has been shown to induce the differentiation of primary hepatocytes in vitro. When actively dividing poorly differentiated human hepatoma-derived (Huh7) cells were cultured in the presence of 1% DMSO, cells became cytologically differentiated and transitioned into a nondividing state, characterized by the induction of hepatocyte-specific genes. Moreover, these cells were highly permissive for acute hepatitis C virus (HCV) infection, and persistent long term infection of these cultures could also be achieved. As HCV naturally replicates in highly differentiated nondividing human hepatocytes, this system may more accurately mimic the conditions under which HCV replicates in vivo than previous models using poorly differentiated rapidly dividing hepatoma cells.

摘要

二甲基亚砜(DMSO)已被证明可在体外诱导原代肝细胞分化。当在1% DMSO存在的情况下培养活跃分裂的低分化人肝癌来源(Huh7)细胞时,细胞在细胞学上发生分化并转变为非分裂状态,其特征是肝细胞特异性基因的诱导。此外,这些细胞对丙型肝炎病毒(HCV)急性感染高度敏感,并且这些培养物也可实现持续的长期感染。由于HCV自然地在高度分化的非分裂人肝细胞中复制,该系统可能比以前使用低分化快速分裂肝癌细胞的模型更准确地模拟HCV在体内复制的条件。