Use of CYP2E1-transfected human liver cell lines in elucidating the actions of ethanol

Alcohol Clin Exp Res. 2005 Sep;29(9):1726-34. doi: 10.1097/01.alc.0000179379.03078.8f.

Abstract

This article represents the proceedings of a symposium at the 2004 RSA Meeting held in Vancouver, Canada. The chairs were Arthur I. Cederbaum and Raj Lakshman. The presentations were (1) ethanol regulates 2,6-sialyltransferase (2,6-ST) gene expression posttranscriptionally by the interaction of a cytosolic binding protein with 2,6-ST mRNA in CYP2E1- and ADH-transfected HepG2 cells, by Raj Lakshman; (2) nature versus nurture: HepG2-E47 cells as a tool to investigate mechanisms of ethanol-mediated potentiation of cell killing, by Jan B. Hoek; (3) ethanol up-regulates profibrogenic connective tissue growth factor gene expression in HepG2 cells via cytochrome P-450 2E1-mediated ethanol oxidation, by Masahiro Konishi; (4) role of calcium and calcium-activated enzymes in CYP2E1-dependent toxicity, by Arthur I Cederbaum; (5) the use of cell lines to characterize the role of CYP2E1 in the metabolism of farnesol, by Dennis Koop; and (6) studies with HepG2 cells that express the two major ethanol-metabolizing enzymes, by Terrence M. Donohue.

MeSH terms

  • Alcohol Dehydrogenase / physiology
  • Calcium / physiology
  • Cell Line
  • Connective Tissue Growth Factor
  • Cytochrome P-450 CYP2E1 / physiology*
  • Ethanol / metabolism
  • Ethanol / toxicity*
  • Farnesol / metabolism
  • Humans
  • Immediate-Early Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / genetics
  • Liver / drug effects*
  • Oxidation-Reduction
  • Sialyltransferases / genetics
  • Transfection
  • Tumor Necrosis Factor-alpha / pharmacology
  • p38 Mitogen-Activated Protein Kinases / physiology

Substances

  • CCN2 protein, human
  • Immediate-Early Proteins
  • Intercellular Signaling Peptides and Proteins
  • Tumor Necrosis Factor-alpha
  • Connective Tissue Growth Factor
  • Ethanol
  • Farnesol
  • Alcohol Dehydrogenase
  • Cytochrome P-450 CYP2E1
  • Sialyltransferases
  • p38 Mitogen-Activated Protein Kinases
  • Calcium