Strategies for immortalization of primary hepatocytes

被引:99
作者
Ramboer, Eva [1 ]
De Craene, Bram [2 ,3 ]
De Kock, Joery [1 ]
Vanhaecke, Tamara [1 ]
Berx, Geert [2 ,3 ]
Rogiers, Vera [1 ]
Vinken, Mathieu [1 ]
机构
[1] Vrije Univ Brussel, Pharmaceut Res Ctr, Dept Toxicol, B-1090 Brussels, Belgium
[2] VIB, Inflammat Res Ctr, Unit Mol & Cellular Oncol, B-9052 Zwijnaarde, Belgium
[3] Univ Ghent, Dept Biomed Mol Biol, B-9052 Ghent, Belgium
基金
欧洲研究理事会;
关键词
Hepatocyte; Proliferation; Senescence; Immortalization; ACUTE LIVER-FAILURE; CELL-CYCLE PROGRESSION; VIRUS CORE PROTEIN; LARGE T-ANTIGEN; DRUG-METABOLIZING-ENZYMES; EPIDERMAL-GROWTH-FACTOR; HUMAN FETAL HEPATOCYTES; NECROSIS-FACTOR-ALPHA; LARGE TUMOR-ANTIGEN; IN-VITRO;
D O I
10.1016/j.jhep.2014.05.046
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The liver has the unique capacity to regenerate in response to a damaging event. Liver regeneration is hereby largely driven by hepatocyte proliferation, which in turn relies on cell cycling. The hepatocyte cell cycle is a complex process that is tightly regulated by several well-established mechanisms. In vitro, isolated hepatocytes do not longer retain this proliferative capacity. However, in vitro cell growth can be boosted by immortalization of hepatocytes. Well-defined immortalization genes can be artificially overexpressed in hepatocytes or the cells can be conditionally immortalized leading to controlled cell proliferation. This paper discusses the current immortalization techniques and provides a state-of-the-art overview of the actually available immortalized hepatocyte-derived cell lines and their applications. (C) 2014 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:925 / 943
页数:19
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