Lysophosphatidylcholine induces keratinocyte differentiation and upregulation of AP-1- and NF-kappaB DNA-binding activity

Acta Derm Venereol. 2004;84(6):433-8. doi: 10.1080/00015550410016930.

Abstract

Lysophosphatidylcholine (lysoPC) is generated by the action of phospholipase A2 on membrane phosphatidylcholine, the most abundant cellular phospholipid. In vitro, lysoPC has pro-inflammatory properties, as it upregulates the expression of adhesion molecules and is a chemoattractant to monocytes and T lymphocytes. It upregulates the expression of a variety of genes including genes encoding growth factors and cyclooxygenase-2 and modulates other cellular responses like proliferation and differentiation. A role for lysoPC as an intracellular messenger transducing signals from membrane-associated receptors has also been suggested. However, the mechanisms behind the diverse actions of lysoPC are poorly understood. In this study we found that lysoPC in non-toxic concentrations caused increased activator protein-1 (AP-1) DNA-binding activity and transglutaminase-1 expression in cultured human keratinocytes. The effects on transglutaminase-1 and AP-1 were dependent on protein kinase C and mitogen-activated protein kinase kinase. In addition, lysoPC caused a rapid and transient increase in DNA-binding activity of nuclear factor-kappaB.

MeSH terms

  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • DNA-Binding Proteins / metabolism
  • Dose-Response Relationship, Drug
  • Humans
  • Keratinocytes / cytology*
  • Keratinocytes / metabolism*
  • Lysophosphatidylcholines / pharmacology*
  • NF-kappa B / metabolism*
  • Transcription Factor AP-1 / metabolism
  • Transglutaminases / metabolism*
  • Up-Regulation / drug effects*

Substances

  • DNA-Binding Proteins
  • Lysophosphatidylcholines
  • NF-kappa B
  • Transcription Factor AP-1
  • Transglutaminases
  • transglutaminase 1