The role of albumin and PPAR-α in differentiation-dependent change of fatty acid profile during differentiation of mesenchymal stem cells to hepatocyte-like cells

Cell Biochem Funct. 2014 Jul;32(5):410-9. doi: 10.1002/cbf.3031. Epub 2014 Mar 3.

Abstract

Differentiation of mesenchymal stem cells (MSCs) to hepatocyte-like cells is associated with morphological and biological changes. In this study, the effect of hepatogenic differentiation on fatty acid profile and the expression of proliferator-activated receptors-α (PPAR-α) have been studied. For this purpose, MSCs isolated from human umbilical cord were differentiated into hepatocyte-like cells on selective culture media. The morphological and biochemical changes, PPAR-α expression and reactive oxygen species (ROS) levels were studied during the differentiation process. Besides, the cells were processed to determine changes in fatty acid profile using gas chromatography analysis. The results showed that hepatic differentiation of the MSCs is associated with a decrease in major polyunsaturated fatty acids in mature hepatocytes, whereas there was an increase in the saturated fatty acid (SFA) levels during hepatocyte maturation. The differentiation-dependent shift in the ratio of SFA/USFA was associated with changes in albumin and PPAR-α expression, whereas changes in fatty acid profile were independent of ROS production and lipid peroxidation in differentiating cells. In conclusion, these data may suggest that hepatocyte formation during the stem cell differentiation is associated with a shift in the fatty acid profile that is probably a normal phenomenon in hepatogenic differentiation of the MSCs.

Keywords: PPAR-α; fatty acid profile; hepatocyte-like cells; reactive oxygen species.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Albumins / genetics
  • Albumins / metabolism*
  • Cell Differentiation*
  • Cells, Cultured
  • Chromatography, Gas
  • Fatty Acids / analysis
  • Fatty Acids / metabolism*
  • Hepatocytes / cytology
  • Hepatocytes / metabolism*
  • Humans
  • Lipid Peroxidation
  • Mesenchymal Stem Cells / cytology*
  • PPAR alpha / genetics
  • PPAR alpha / metabolism*
  • RNA, Messenger / metabolism
  • Reactive Oxygen Species / metabolism
  • Umbilical Cord / cytology

Substances

  • Albumins
  • Fatty Acids
  • PPAR alpha
  • RNA, Messenger
  • Reactive Oxygen Species