Inhibition of peroxisome proliferator-activated receptor (PPAR)-mediated keratinocyte differentiation by lipoxygenase inhibitors

Biochem J. 2002 Sep 15;366(Pt 3):901-10. doi: 10.1042/BJ20020377.

Abstract

Lipoxygenase (LOX) metabolites from arachidonic acid and linoleic acid have been implicated in atherosclerosis, inflammation, keratinocyte differentiation and tumour progression. We previously showed that peroxisome proliferator-activated receptors (PPARs) play a role in keratinocyte differentiation and that the PPARalpha ligand 8S-hydroxyeicosatetraenoic acid is important in this process. We hypothesized that blocking LOX activity would block PPAR-mediated keratinocyte differentiation. Three LOX inhibitors, nordihydroguaiaretic acid, quercetin and morin, were studied for their effects on primary keratinocyte differentiation and PPAR activity. All three LOX inhibitors blocked calcium-induced expression of the differentiation marker keratin 1. In addition, activity of a PPAR-responsive element was inhibited in the presence of all three inhibitors, and this effect was mediated primarily through PPARalpha and PPARgamma. LOX inhibitors decreased the activity of a chimaeric PPAR-Gal4-ligand-binding domain reporter system and this effect was reversed by addition of PPAR ligands. Ligand-binding studies revealed that the LOX inhibitors bind directly to PPARs and demonstrate a novel mechanism for these inhibitors in altering PPAR-mediated gene expression.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Arachidonic Acid / metabolism
  • Blotting, Northern
  • Blotting, Western
  • Cell Differentiation
  • Cell Survival
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Enzyme Inhibitors / pharmacology
  • Genes, Reporter
  • Inhibitory Concentration 50
  • Keratinocytes / metabolism*
  • Keratins / metabolism
  • Ligands
  • Linoleic Acid / metabolism
  • Lipoxygenase / metabolism*
  • Mice
  • Protein Binding
  • Receptors, Cytoplasmic and Nuclear / metabolism*
  • Time Factors
  • Transcription Factors / metabolism*

Substances

  • Enzyme Inhibitors
  • Ligands
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Arachidonic Acid
  • Keratins
  • Linoleic Acid
  • Lipoxygenase