| Literature DB >> 27259983 |
Jianxing Zeng1,2, Yingying Jing1, Rongyu Shi1,2, Xiaorong Pan1,2, Fobao Lai1,2, Wenting Liu1, Rong Li1, Lu Gao1, Xiaojuan Hou1, Mengchao Wu3, Lixin Wei1.
Abstract
Autophagy plays important roles in self-renewal and differentiation of stem cells. Hepatic progenitor cells (HPCs) are thought to have the ability of self-renewal as well as possess a bipotential capacity, which allows them to differentiate into both hepatocytes and bile ductular cells. However, how autophagy contributes to self-renewal and differentiation of hepatic progenitor cells is not well understood. In this study, we use a well-established rat hepatic progenitor cell lines called WB-F344, which is treated with 3.75 mM sodium butyrate (SB) to promote the differentiation of WB-F344 along the biliary phenotype. We found that autophagy was decreased in the early stage of biliary differentiation, and maintained a low level at the late stage. Activation of autophagy by rapamycin or starvation suppressed the biliary differentiation of WB-F344. Further study reported that autophagy inhibited Notch1 signaling pathway, which contributed to biliary differentiation and morphogenesis. In conclusions, autophagy regulates biliary differentiation of hepatic progenitor cells through Notch1 signaling pathway.Entities:
Keywords: Notch1; autophagy; biliary differentiation; hepatic progenitor cells
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Year: 2016 PMID: 27259983 PMCID: PMC4934079 DOI: 10.1080/15384101.2016.1181234
Source DB: PubMed Journal: Cell Cycle ISSN: 1551-4005 Impact factor: 4.534