Advancements in MAFLD Modeling with Human Cell and Organoid Models

被引:14
作者
Wang, Shi-Xiang [1 ]
Yan, Ji-Song [1 ,2 ]
Chan, Yun-Shen [1 ]
机构
[1] Guangzhou Lab, 9 Xing Dao Huan Bei Rd, Guangzhou 510005, Peoples R China
[2] Yunnan Univ, Sch Life Sci, Kunming 650500, Yunnan, Peoples R China
关键词
MAFLD; human model; cell culture; organoid; microfluidics; NONALCOHOLIC FATTY LIVER; PLURIPOTENT STEM-CELLS; SINUSOIDAL ENDOTHELIAL-CELLS; HEPATIC INSULIN-RESISTANCE; HEPATOCYTE-LIKE CELLS; IN-VITRO MODEL; GENE-EXPRESSION; LIPID-ACCUMULATION; STELLATE CELLS; EFFICIENT DIFFERENTIATION;
D O I
10.3390/ijms231911850
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic (dysfunction) associated fatty liver disease (MAFLD) is one of the most prevalent liver diseases and has no approved therapeutics. The high failure rates witnessed in late-phase MAFLD drug trials reflect the complexity of the disease, and how the disease develops and progresses remains to be fully understood. In vitro, human disease models play a pivotal role in mechanistic studies to unravel novel disease drivers and in drug testing studies to evaluate human-specific responses. This review focuses on MAFLD disease modeling using human cell and organoid models. The spectrum of patient-derived primary cells and immortalized cell lines employed to model various liver parenchymal and non-parenchymal cell types essential for MAFLD development and progression is discussed. Diverse forms of cell culture platforms utilized to recapitulate tissue-level pathophysiology in different stages of the disease are also reviewed.
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页数:28
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