Guangzhou Laboratory, No. 9 Xing Dao Huan Bei Road, Guangzhou International Bio Island, Guangzhou 510005, China.
School of Life Sciences, Yunnan University, Kunming 650500, China.
Int J Mol Sci. 2022 Oct 6;23(19):11850. doi: 10.3390/ijms231911850.
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.
代谢(功能)相关脂肪性肝病(MAFLD)是最常见的肝脏疾病之一,目前尚无批准的治疗方法。晚期 MAFLD 药物试验的高失败率反映了该疾病的复杂性,其发病机制和进展仍有待充分了解。在体外,人类疾病模型在阐明新的疾病驱动因素的机制研究和评估人类特异性反应的药物测试研究中发挥着关键作用。本综述重点介绍了使用人类细胞和类器官模型进行的 MAFLD 疾病建模。讨论了用于模拟各种对 MAFLD 发生和发展至关重要的肝实质和非实质细胞类型的患者来源的原代细胞和永生化细胞系的范围。还回顾了用于再现不同疾病阶段组织水平病理生理学的各种细胞培养平台。