Porcine Adipose-Derived Mesenchymal Stem Cells Retain Their Stem Cell Characteristics and Cell Activities While Enhancing the Expression of Liver-Specific Genes after Acute Liver Failure

Int J Mol Sci. 2016 Jan 5;17(1):62. doi: 10.3390/ijms17010062.

Abstract

Acute liver failure (ALF) is a kind of complicated syndrome. Furthermore, adipose-derived mesenchymal stem cells (ADMSCs) can serve as a useful cell resource for autotransplantation due to their abundance and micro-invasive accessability. However, it is unknown how ALF will influence the characteristics of ADMSCs and whether ADMSCs from patients suffering from end-stage liver diseases are potential candidates for autotransplantation. This study was designed to compare various properties of ALF-derived ADMSCs with normal ADMSCs in pig models, with regard to their cellular morphology, cell proliferative ability, cell apoptosis, expression of surface antigens, mitochondrial and lysosomal activities, multilineage potency, and expression of liver-specific genes. Our results showed that ALF does not influence the stem cell characteristics and cell activities of ADMSCs. Intriguingly, the expression levels of several liver-specific genes in ALF-derived ADMSCs are higher than in normal ADMSCs. In conclusion, our findings indicate that the stem cell characteristics and cell activities of ADMSCs were not altered by ALF and these cells can serve as a new source for regenerative medicine.

Keywords: acute liver failure (ALF); adipose-derived mesenchymal stem cells (ADMSCs); autotransplantation; biological characteristics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology*
  • Adipose Tissue / metabolism
  • Animals
  • Antigens, CD / analysis
  • Antigens, CD / genetics
  • Apoptosis
  • Cell Differentiation
  • Cell Proliferation
  • Gene Expression Regulation
  • Humans
  • Liver / metabolism
  • Liver / pathology
  • Liver Failure, Acute / genetics
  • Liver Failure, Acute / pathology
  • Liver Failure, Acute / therapy*
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Swine
  • Transplantation, Autologous

Substances

  • Antigens, CD