Direct chemical induction of hepatocyte‐like cells with capacity for liver repopulation

重编程 肝细胞 细胞生物学 生物 肝细胞核因子4 细胞 肝细胞核因子 转录因子 核受体 生物化学 体外 基因
作者
Ya Na Bai,Zhenghao Yang,Xiaochan Xu,Wanqiu Ding,Juntian Qi,Feng Liu,Xiaoxiao Wang,Bin Zhou,Wenpeng Zhang,Xiaomei Zhuang,Guanglu Li,Yang Zhao
出处
期刊:Hepatology [Wiley]
卷期号:77 (5): 1550-1565 被引量:8
标识
DOI:10.1002/hep.32686
摘要

Background and Aims: Cell fate can be directly reprogrammed from accessible cell types (e.g., fibroblasts) into functional cell types by exposure to small molecule stimuli. However, no chemical reprogramming method has been reported to date that successfully generates functional hepatocyte‐like cells that can repopulate liver tissue, casting doubt over the feasibility of chemical reprogramming approaches to obtain desirable cell types for therapeutic applications. Approach and Results: Here, through chemical induction of phenotypic plasticity, we provide a proof‐of‐concept demonstration of the direct chemical reprogramming of mouse fibroblasts into functional hepatocyte‐like cells using exposure to small molecule cocktails in culture medium to successively stimulate endogenous expression of master transcription factors associated with hepatocyte development, such as hepatocyte nuclear factor 4a, nuclear receptor subfamily 1, group I, member 2, and nuclear receptor subfamily 1, group H, member 4. RNA sequencing analysis, metabolic assays, and in vivo physiological experiments show that chemically induced hepatocytes (CiHeps) exhibit comparable activity and function to primary hepatocytes, especially in liver repopulation to rescue liver failure in fumarylacetoacetate hydrolase−/−recombination activating gene 2−/−interleukin 2 receptor, gamma chain−/− mice in vivo. Single‐cell RNA‐seq further revealed that gastrointestinal‐like and keratinocyte‐like cells were induced along with CiHeps, resembling the activation of an intestinal program within hepatic reprogramming as described in transgenic approaches. Conclusions Our findings show that direct chemical reprogramming can generate hepatocyte‐like cells with high‐quality physiological properties, providing a paradigm for establishing hepatocyte identity in fibroblasts and demonstrating the potential for chemical reprogramming in organ/tissue repair and regeneration therapies. Export
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