Mesenchymal-Epithelial Transition in Culture of Stromal Progenitor Cells Isolated from the Liver of a Patient with Alcoholic Cirrhosis

Bull Exp Biol Med. 2016 Nov;162(1):115-119. doi: 10.1007/s10517-016-3559-z. Epub 2016 Nov 23.

Abstract

The cells isolated from biopsy specimen of a patient with alcoholic liver cirrhosis and cultured under standard conditions for obtaining stromal cell culture clearly diverged during early passages into two morphologically and phenotypically different subtypes: epithelial and mesenchymal. Mesenchymal cells expressed CD90 and CD44 and epithelial cells expressed CD166, CD227, and hepatocyte growth factor receptor Met. Starting from passage 6, the culture underwent spontaneous morphological changes and by passages 8-10 contained only epithelium-like cells. CD90 and CD44 expression disappeared, CD166 and CD227 expression remained unchanged, and Met expression increased. A small fraction of cells expressed GATA-4, HNF3β, HNF1α, and HNF4α. After addition of inducers of hepatogeneic differentiation, the cells started producing albumin.

Keywords: hepatogeneic differentiation; liver stromal progenitor cells; mesenchymal-epithelial transition.

Publication types

  • Case Reports

MeSH terms

  • Albumins / biosynthesis
  • Albumins / genetics
  • Antigens, CD / genetics
  • Antigens, CD / metabolism
  • Biomarkers / metabolism
  • Cell Differentiation
  • Cell Proliferation
  • Epithelial-Mesenchymal Transition / genetics*
  • GATA4 Transcription Factor / genetics
  • GATA4 Transcription Factor / metabolism
  • Gene Expression
  • Hepatocyte Nuclear Factor 1-alpha / genetics
  • Hepatocyte Nuclear Factor 1-alpha / metabolism
  • Hepatocyte Nuclear Factor 3-beta / genetics
  • Hepatocyte Nuclear Factor 3-beta / metabolism
  • Hepatocyte Nuclear Factor 4 / genetics
  • Hepatocyte Nuclear Factor 4 / metabolism
  • Humans
  • Liver / metabolism*
  • Liver / pathology
  • Liver Cirrhosis, Alcoholic / genetics*
  • Liver Cirrhosis, Alcoholic / metabolism
  • Liver Cirrhosis, Alcoholic / pathology
  • Mesenchymal Stem Cells / metabolism*
  • Mesenchymal Stem Cells / pathology
  • Primary Cell Culture
  • Proto-Oncogene Proteins c-met / genetics
  • Proto-Oncogene Proteins c-met / metabolism
  • Stem Cells / metabolism*
  • Stem Cells / pathology

Substances

  • Albumins
  • Antigens, CD
  • Biomarkers
  • FOXA2 protein, human
  • GATA4 Transcription Factor
  • GATA4 protein, human
  • HNF1A protein, human
  • HNF4A protein, human
  • Hepatocyte Nuclear Factor 1-alpha
  • Hepatocyte Nuclear Factor 4
  • Hepatocyte Nuclear Factor 3-beta
  • MET protein, human
  • Proto-Oncogene Proteins c-met