Hepatoblast-like progenitor cells derived from embryonic stem cells can repopulate livers of mice

Gastroenterology. 2010 Dec;139(6):2158-2169.e8. doi: 10.1053/j.gastro.2010.08.042. Epub 2010 Aug 27.

Abstract

Background & aims: Hepatocyte-like cells can be derived from pluripotent stem cells such as embryonic stem (ES) cells, but ES cell-derived hepatic cells with extensive capacity to repopulate liver have not been identified. We aimed to identify and purify ES cell-derived hepatoblast-like progenitor cells and to explore their capacity for liver repopulation in mice after in vitro expansion.

Methods: Unmanipulated mouse ES cells were cultured under defined conditions and allowed to undergo stepwise hepatic differentiation. The derived hepatic cells were examined by morphologic, fluorescence-activated cell sorting, gene expression, and clonal expansion analyses. The capacities of ES cell-derived hepatic progenitor cells to repopulate liver were investigated in mice that were deficient in fumarylacetoacetate hydrolase (Fah) (a model of liver injury).

Results: Mouse ES cells were induced to differentiate into a population that contained hepatic progenitor cells; this population included cells that expressed epithelial cell adhesion molecule (EpCAM) but did not express c-Kit. Clonal hepatic progenitors that arose from single c-Kit(-)EpCAM(+) cells could undergo long-term expansion and maintain hepatoblast-like characteristics. Enriched c-Kit(-)EpCAM(+) cells and clonally expanded hepatic progenitor cells repopulated the livers of Fah-deficient mice without inducing tumorigenesis.

Conclusions: ES cell-derived c-Kit(-)EpCAM(+) cells contain a population of hepatoblast-like progenitor cells that can repopulate livers of mice.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / physiology
  • Cell Division / physiology
  • Cell Separation / methods
  • Cells, Cultured
  • Disease Models, Animal
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism
  • Graft Survival / physiology
  • Hepatocytes / cytology*
  • Hydrolases / genetics
  • Liver Diseases / pathology*
  • Liver Diseases / therapy*
  • Liver Regeneration
  • Mice
  • Mice, Mutant Strains
  • Proto-Oncogene Proteins c-kit / metabolism
  • Stem Cell Transplantation*

Substances

  • Proto-Oncogene Proteins c-kit
  • Hydrolases
  • fumarylacetoacetase