Steatotic liver: a suitable source for the isolation of hepatic progenitor cells

Liver Int. 2011 Sep;31(8):1231-8. doi: 10.1111/j.1478-3231.2011.02609.x.

Abstract

Background: Alternative and/or complementary sources of cells such as hepatic progenitor cells (HPC) are under investigation for hepatic cell therapy purposes. Steatotic livers are those most commonly rejected for clinical transplantation and are also unsuitable for good quality hepatocyte isolation.

Aim: Taken together these two facts, our aim was to investigate whether they could represent a suitable source for the isolation of progenitor cells.

Methods: Rats fed for 7 weeks with methionine-choline deficient diets showing proved steatotic signs (i.e. increase in hepatic lipids; macrovesicular steatosis) and steatotic and normal human liver samples were used to study the expression of HPC markers and to isolate these cells.

Results: In the liver of the steatotic rats there was a significant increase in HPC (known as oval cells in rodents) markers such as Thy-1, epithelial cell adhesion molecule (EpCAM) and OV-6 (2-, 3- and 5-fold increase respectively). Additionally, there was an increase in the yield of isolated oval cells compared to control rats. Similarly, studies using human livers clearly confirmed an increase in the expression of HPC markers in the steatotic tissue and a significant rise in the number of isolated progenitor cells (EpCAM+, Thy-1+, OV-6+) (10, 12 and 11.6 × 10(4) cells/g of tissue respectively).

Conclusions: These data suggest that steatotic livers, discarded for orthotopic liver transplantation and hepatocyte isolation, could be a suitable source for large scale isolation of HPC which might be potential candidates in liver cell therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / metabolism
  • Antigens, Neoplasm / metabolism
  • Biomarkers / metabolism
  • Cell Adhesion Molecules / metabolism
  • Cell Separation* / methods
  • Choline Deficiency / complications
  • Disease Models, Animal
  • Epithelial Cell Adhesion Molecule
  • Fatty Liver / etiology
  • Fatty Liver / metabolism
  • Fatty Liver / pathology*
  • Flow Cytometry
  • Humans
  • Liver / metabolism
  • Liver / pathology*
  • Male
  • Methionine / deficiency
  • Rats
  • Stem Cells / metabolism
  • Stem Cells / pathology*
  • Thy-1 Antigens / metabolism
  • Time Factors

Substances

  • Antigens, Differentiation
  • Antigens, Neoplasm
  • Biomarkers
  • Cell Adhesion Molecules
  • EPCAM protein, human
  • Epithelial Cell Adhesion Molecule
  • Thy-1 Antigens
  • oval cell marker OV-6
  • Methionine