Yes‐associated protein promotes the proliferation and differentiation of liver progenitor cells during liver fibrosis

祖细胞 纤维化 LGR5型 癌症研究 细胞生长 河马信号通路 肝细胞 生物 干细胞标记物 干细胞 病理 Wnt信号通路 信号转导 细胞生物学 医学 遗传学 生物化学 体外
作者
Zhenyang Shen,Weiming Dai,Yuecheng Guo,Junjun Wang,Bo Shen,Binghang Li,Lungen Lu,Xiaobo Cai
出处
期刊:The FASEB Journal [Wiley]
卷期号:37 (5)
标识
DOI:10.1096/fj.202201919r
摘要

Abstract Liver fibrosis is closely related to the proliferation and differentiation of liver progenitor cells (LPCs). Yes‐associated protein (YAP) is a key effector molecule of the Hippo signaling pathway and plays an important role in regulating cell proliferation and liver homeostasis. However, its role in LPCs proliferation and differentiation during liver fibrosis are not well understood. Using immunohistochemistry, immunofluorescence staining, quantitative PCR and Western blotting, we discovered that LPCs expansion and enhanced YAP expression in LPCs in either choline‐deficient, ethionine‐supplemented (CDE) diet or 3,5‐diethoxycarbonyl‐1,4‐dihydrocollidine (DDC) diet‐induced fibrotic mice, as well as in patients with liver fibrosis. By injecting adeno‐associated virus vectors under the transcriptional control of Lgr5 promoter, we found that targeted knockdown of YAP in LPCs attenuated the CDE/DDC diet‐induced ductular reaction and liver fibrosis. Using EdU incorporation and Cell Counting Kit‐8 assays, we demonstrated that YAP can modulate LPCs proliferation. Importantly, spleen transplantation of YAP‐overexpressing LPCs improved their ability to differentiate into hepatocytes and alleviated carbon tetrachloride‐induced liver fibrosis. Collectively, our findings indicate that LPCs expansion and differentiation during liver fibrosis could be modulated by YAP, further suggesting the possibility of manipulating YAP expression in LPCs as a potential treatment for chronic liver diseases.
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