诱导多能干细胞
肝损伤
酒精性肝病
肝细胞
肝病
细胞凋亡
癌症研究
生物
酒
干细胞
体外
细胞生物学
医学
生物信息学
药理学
内科学
生物化学
胚胎干细胞
肝硬化
基因
作者
Lipeng Tian,Neha Prasad,Yoon-Young Jang
出处
期刊:Methods in molecular biology
日期:2014-01-01
卷期号:: 271-283
被引量:18
标识
DOI:10.1007/7651_2014_168
摘要
Alcohol consumption has long been associated with a majority of liver diseases and has been found to influence both fetal and adult liver functions. In spite of being one of the major causes of morbidity and mortality in the world, currently, there are no effective strategies that can prevent or treat alcoholic liver disease (ALD), due to a lack of human-relevant research models. Recent success in generation of functionally active mature hepatocyte-like cells from human-induced pluripotent cells (iPSCs) enables us to better understand the effects of alcohol on liver functions. Here, we describe the method and effect of alcohol exposure on multistage hepatic cell types derived from human iPSCs, in an attempt to recapitulate the early stages of liver tissue injury associated with ALD. We exposed different stages of iPSC-induced hepatic cells to ethanol at a pathophysiological concentration. In addition to stage-specific molecular markers, we measured several key cellular parameters of hepatocyte injury, including apoptosis, proliferation, and lipid accumulation.
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