Induction of hepatic differentiation in embryonic stem cells by co-culture with embryonic cardiac mesoderm

Surgery. 2003 Aug;134(2):189-96. doi: 10.1067/msy.2003.225.

Abstract

Background: Modifications in vitro have been used to direct embryonic stem (ES) cells toward endodermal phenotypes including hepatocytes; however, developmental correlates and evidence of biologic activity is lacking, and critical cell-cell interactions have not been investigated. In this study, we hypothesized that cardiac mesoderm (CM) signals ES cells in co-culture to undergo differentiation toward early hepatocyte lineage as determined by morphology and induction of genes essential for endodermal competence and hepatocyte development.

Methods: Green fluorescent protein ES derived from A129 mice were cultured with or without embryonic chick cardiac mesoderm. Cultures from day 1, 2, and 4 were analyzed for colony formation and ES morphology and 10(6) ES-derived cells were isolated for mRNA analysis.

Results: ES in co-culture with CM displayed colony formation, polymorphic appearance, and definitive interface with CM. In addition, ES + CM co-culture activated crucial transcription factors (sox 17alpha, HNF3beta, and GATA 4) required for hepatocyte development by day 1. mRNA for albumin and especially a-fetoprotein were also increased by culture days 2 and 4.

Conclusions: ES cells co-cultured with CM display morphology and gene expression pattern required for hepatocyte differentiation and appear to recapitulate the molecular events of hepatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / genetics
  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Chick Embryo
  • Coculture Techniques
  • DNA-Binding Proteins / metabolism
  • Embryo, Mammalian / cytology
  • GATA4 Transcription Factor
  • Green Fluorescent Proteins
  • Heart / embryology*
  • Hepatocyte Nuclear Factor 3-beta
  • Indicators and Reagents
  • Liver / cytology
  • Liver / embryology*
  • Luminescent Proteins
  • Mesoderm / physiology*
  • Mice
  • Mice, Inbred Strains
  • Nuclear Proteins / metabolism
  • Proteins / metabolism
  • RNA, Messenger / metabolism
  • Stem Cells / cytology*
  • Stem Cells / metabolism
  • Time Factors
  • Transcription Factors / metabolism
  • alpha-Fetoproteins / genetics

Substances

  • Albumins
  • DNA-Binding Proteins
  • Foxa2 protein, mouse
  • GATA4 Transcription Factor
  • Indicators and Reagents
  • Luminescent Proteins
  • Nuclear Proteins
  • Proteins
  • RNA, Messenger
  • Transcription Factors
  • alpha-Fetoproteins
  • Hepatocyte Nuclear Factor 3-beta
  • Green Fluorescent Proteins