Lipid rafts and Fas/FasL pathway may involve in elaidic acid-induced apoptosis of human umbilical vein endothelial cells

J Agric Food Chem. 2014 Jan 22;62(3):798-807. doi: 10.1021/jf404834e. Epub 2014 Jan 8.

Abstract

Our previous study showed that trans-fatty acids can cause apoptosis of endothelial cells through the caspase pathway and the mitochondrial pathway. The objective of this study was to explore how trans-fatty acids activate the caspase pathway, whether there exist specific receptors induced apoptosis by comparing normal cells and non-rafts cells treated with elaidic acid (9t18:1) and oleic acid (9c18:1), respectively. Compared to normal cells treated with 9t18:1, the cell viability increased by 13% and the number of apoptotic cells decreased by 3% in non-rafts cells treated with 9t18:1 (p < 0.05), and the expression levels of pro-apoptotic proteins such as caspase-3, -8, -9, Bax, and Bid decreased, and expression of antiapoptotic protein Bcl-2 increased (p < 0.05). In addition, Fas/FasL expression in cell membrane decreased significantly (p < 0.05). In conclusion, the lipid rafts and Fas/FasL pathway may involve in 9t18:1-induced apoptosis of human umbilical vein endothelial cells.

Keywords: apoptosis; human umbilical vein endothelial cells; lipid raft; receptor; trans-fatty acid.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis / drug effects*
  • Caspase 3 / metabolism
  • Caspase 8 / metabolism
  • Cell Survival
  • Fas Ligand Protein / metabolism*
  • Human Umbilical Vein Endothelial Cells / cytology*
  • Human Umbilical Vein Endothelial Cells / metabolism*
  • Humans
  • Membrane Microdomains / metabolism*
  • Oleic Acid / chemistry
  • Oleic Acid / metabolism*
  • Oleic Acids
  • Signal Transduction
  • fas Receptor / metabolism*

Substances

  • FAS protein, human
  • Fas Ligand Protein
  • Oleic Acids
  • fas Receptor
  • Oleic Acid
  • elaidic acid
  • Caspase 3
  • Caspase 8