Hepato-biliary profile of potential candidate liver progenitor cells from healthy rat liver

World J Gastroenterol. 2012 Jul 21;18(27):3511-9. doi: 10.3748/wjg.v18.i27.3511.

Abstract

Aim: To evaluate the presence of progenitor cells in healthy adult rat liver displaying the equivalent advanced hepatogenic profile as that obtained in human.

Methods: Rat fibroblastic-like liver derived cells (rFLDC) were obtained from collagenase-isolated liver cell suspensions and characterized and their phenotype profile determined using flow cytometry, immunocytochemistry, reverse transcription polymerase chain reaction and functional assays.

Results: rFLDC exhibit fibroblastoid morphology, express mesenchymal (CD73, CD90, vimentin, α-smooth muscle actin), hepatocyte (UGT1A1, CK8) and biliary (CK19) markers. Moreover, these cells are able to store glycogen, and have glucose 6 phosphatase activity, but not UGT1A1 activity. Under the hepatogenic differentiation protocol, rFLDC display an up-regulation of hepatocyte markers expression (albumin, tryptophan 2,3-dioxygenase, G6Pase) correlated to a down-regulation of the expression of the biliary marker CK19.

Conclusion: Advanced hepatic features observed in human liver progenitor cells could not be demonstrated in rFLDC. However, we demonstrated the presence of an original rodent hepato-biliary cell type.

Keywords: Hepato biliary profile; Hepatogenic differentiation; Liver; Progenitor cell; Rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bile Ducts / cytology
  • Bile Ducts / metabolism
  • Bile Ducts / physiology*
  • Biomarkers / metabolism
  • Cell Differentiation*
  • Cell Proliferation
  • Cell Separation / methods
  • Cell Shape
  • Cells, Cultured
  • Energy Metabolism
  • Fibroblasts / metabolism
  • Fibroblasts / physiology*
  • Flow Cytometry
  • Gene Expression Regulation
  • Hepatocytes / metabolism
  • Hepatocytes / physiology*
  • Immunohistochemistry
  • Liver / cytology
  • Liver / metabolism
  • Liver / physiology*
  • Male
  • Phenotype
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stem Cells / metabolism
  • Stem Cells / physiology*
  • Time Factors

Substances

  • Biomarkers