Tumor necrosis factor-inducible gene 6 reprograms hepatic stellate cells into stem-like cells, which ameliorates liver damage in mouse

Biomaterials. 2019 Oct:219:119375. doi: 10.1016/j.biomaterials.2019.119375. Epub 2019 Jul 22.

Abstract

Liver fibrosis is a major characteristic of liver disease. When the liver is damaged, quiescent hepatic stellate cells (HSCs) transdifferentiate into proliferative myofibroblastic/activated HSCs, which are the main contributors to liver fibrosis. Hence, a strategy for regulating HSC activation is important in the treatment of liver disease. Tumor necrosis factor-inducible gene 6 protein (TSG-6), a cytokine released from mesenchymal stem cells (MSCs), influences MSC stemness. Therefore, we investigated the biological effect of TSG-6 on HSCs. Human primary HSCs treated with TSG-6 showed significant downregulation of HSC activation markers and upregulation of senescence markers. TSG-6 promoted these cells to express stem cell markers and form spherical organoids, which exhibited elevated expression of stemness-related genes. These organoids differentiated into functional hepatocytic cells under specific culture conditions. Organoids derived from TSG-6-treated HSCs improved livers in organoid transplant mice subjected to CCl4 treatment (which induces liver fibrosis). Furthermore, HSC transdifferentiation by TSG-6 was mediated by Yes-associated protein 1. These findings demonstrate that TSG-6 induces the conversion of HSCs into stem cell-like cells in vitro and that organoids derived from TSG-6-treated HSCs can restore fibrotic liver, suggesting that direct reprogramming of HSCs by TSG-6 can be a useful strategy to control liver disease.

Keywords: HSC; Liver regeneration; Organoid; Reprogramming; TSG-6.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Biomarkers / metabolism
  • Cell Adhesion Molecules / pharmacology*
  • Cell Line
  • Cells, Cultured
  • Cellular Reprogramming* / drug effects
  • Cellular Senescence / drug effects
  • Hepatic Stellate Cells / drug effects
  • Hepatic Stellate Cells / metabolism*
  • Humans
  • Liver / metabolism*
  • Liver / pathology*
  • Liver / physiopathology
  • Liver Cirrhosis / pathology
  • Male
  • Mice, Inbred C57BL
  • Organoids / drug effects
  • Organoids / metabolism
  • Stem Cells / drug effects
  • Stem Cells / metabolism*

Substances

  • Biomarkers
  • Cell Adhesion Molecules