Liver three-dimensional cellular models for high-throughput chemical testing

被引:40
作者
Yang, Shu [1 ]
Ooka, Masato [1 ]
Margolis, Ryan Jared [1 ]
Xia, Menghang [1 ]
机构
[1] NIH, Div Preclin Innovat, Natl Ctr Adv Translat Sci, Bethesda, MD 20892 USA
来源
CELL REPORTS METHODS | 2023年 / 3卷 / 03期
基金
美国国家卫生研究院;
关键词
PRIMARY HUMAN HEPATOCYTES; PLURIPOTENT STEM-CELLS; IN-VITRO MODEL; HEPARG CELLS; TUMOR SPHEROIDS; DRUG-METABOLISM; TOXICITY; CULTURE; GENERATION; HEPATOTOXICITY;
D O I
10.1016/j.crmeth.2023.100432
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Drug-induced hepatotoxicity is a leading cause of drug withdrawal from the market. High-throughput screening utilizing in vitro liver models is critical for early-stage liver toxicity testing. Traditionally, monolayer human hepatocytes or immortalized liver cell lines (e.g., HepG2, HepaRG) have been used to test compound liver toxicity. However, monolayer-cultured liver cells sometimes lack the metabolic competence to mimic the in vivo condition and are therefore largely appropriate for short-term toxicological testing. They may not, however, be adequate for identifying chronic and recurring liver damage caused by drugs. Recently, several three-dimensional (3D) liver models have been developed. These 3D liver models better recapitulate normal liver function and metabolic capacity. This review describes the current development of 3D liver models that can be used to test drugs/chemicals for their pharmacologic and toxicologic effects, as well as the advantages and limitations of using these 3D liver models for high-throughput screening.
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收藏
页数:14
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