Autophagy regulates biliary differentiation of hepatic progenitor cells through Notch1 signaling pathway

Cell Cycle. 2016 Jun 17;15(12):1602-10. doi: 10.1080/15384101.2016.1181234. Epub 2016 Jun 3.

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.

Keywords: Notch1; autophagy; biliary differentiation; hepatic progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy / drug effects
  • Autophagy / genetics
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • Bile Ducts / cytology
  • Bile Ducts / drug effects
  • Bile Ducts / metabolism
  • Butyric Acid / pharmacology*
  • Cell Differentiation / drug effects
  • Cell Line
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Gene Expression Regulation
  • Hepatocyte Nuclear Factor 1-beta / genetics
  • Hepatocyte Nuclear Factor 1-beta / metabolism
  • Hepatocyte Nuclear Factor 6 / genetics
  • Hepatocyte Nuclear Factor 6 / metabolism
  • Hepatocytes / cytology
  • Hepatocytes / drug effects*
  • Hepatocytes / metabolism
  • Jagged-1 Protein / genetics
  • Jagged-1 Protein / metabolism
  • Keratin-19 / genetics
  • Keratin-19 / metabolism
  • Liver / cytology
  • Liver / drug effects
  • Liver / metabolism
  • Rats
  • Rats, Inbred F344
  • Receptor, Notch1 / genetics*
  • Receptor, Notch1 / metabolism
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Signal Transduction
  • Sirolimus / pharmacology*
  • Stem Cells / cytology
  • Stem Cells / drug effects*
  • Stem Cells / metabolism
  • Transcription Factor HES-1 / genetics
  • Transcription Factor HES-1 / metabolism

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • Hairy, HRT1 protein
  • Hepatocyte Nuclear Factor 6
  • Hes1 protein, rat
  • Hes5 protein, rat
  • Hnf1b protein, rat
  • Jag1 protein, rat
  • Jagged-1 Protein
  • Keratin-19
  • Notch1 protein, rat
  • Onecut1 protein, rat
  • Receptor, Notch1
  • Repressor Proteins
  • Transcription Factor HES-1
  • Butyric Acid
  • Hepatocyte Nuclear Factor 1-beta
  • Sirolimus