Generating hepatic cell lineages from pluripotent stem cells for drug toxicity screening

被引:52
作者
Baxter, Melissa A. [1 ]
Rowe, Cliff [1 ]
Alder, Jane [3 ]
Harrison, Sean [1 ]
Hanley, Karen Piper [1 ]
Park, B. Kevin [2 ]
Kitteringham, Neil R. [2 ]
Goldring, Chris E. [2 ]
Hanley, Neil A. [1 ]
机构
[1] Univ Manchester, Sch Biomed, Manchester Acad Hlth Sci Ctr, Manchester M13 9PT, Lancs, England
[2] Univ Liverpool, MRC Ctr Drug Safety Sci, Dept Pharmacol & Therapeut, Liverpool L69 3GE, Merseyside, England
[3] Univ Cent Lancashire, Sch Pharm & Pharmaceut Sci, Preston PR1 2HE, Lancs, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
HEPATOCYTE-LIKE CELLS; IN-VITRO DIFFERENTIATION; EFFICIENT DIFFERENTIATION; LIVER DEVELOPMENT; GENE-EXPRESSION; CYTOCHROME-P450; EXPRESSION; DEFINITIVE ENDODERM; PROGENITOR CELLS; NITRIC-OXIDE; ONCOSTATIN-M;
D O I
10.1016/j.scr.2010.02.002
中图分类号
Q813 [细胞工程];
学科分类号
100113 [医学细胞生物学];
摘要
Hepatotoxicity is an enormous and increasing problem for the pharmaceutical industry. Early detection of problems during the drug discovery pathway is advantageous to minimize costs and improve patient safety. However, current cellular models are sub-optimal. This review addresses the potential use of pluripotent stem cells in the generation of hepatic cell lineages. It begins by highlighting the scale of the problem faced by the pharmaceutical industry, the precise nature of drug-induced liver injury and where in the drug discovery pathway the need for additional cell models arises. Current research is discussed, mainly for generating hepatocyte-like cells rather than other liver cell-types. In addition, an effort is made to identify where some of the major barriers remain in translating what is currently hypothesis-driven laboratory research into meaningful platform technologies for the pharmaceutical industry. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:4 / 22
页数:19
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