Hydrogen peroxide stimulates transcription of c-jun in vascular smooth muscle cells: role of arachidonic acid

Oncogene. 1993 Oct;8(10):2759-64.

Abstract

We reported previously that hydrogen peroxide induces DNA synthesis in rat aortic smooth muscle (RASM) cells. In the present paper we studied the mechanism by which hydrogen peroxide induces c-jun mRNA, an early response gene whose activation is required for mitogen-stimulated cell growth. Hydrogen peroxide induced c-jun mRNA in growth-arrested RASM cells in a time dependent manner. This stimulation was significantly inhibited by mepacrine, a phospholipase A2 (PLA2) inhibitor. Arachidonic acid, a PLA2 product, also increased c-jun mRNA with a time course similar to that of hydrogen peroxide. The increases in c-jun mRNA induced by hydrogen peroxide and arachidonic acid were significantly reduced (55%) by down-regulation of protein kinase C with a phorbol ester. Furthermore, the effect of hydrogen peroxide on c-jun mRNA was also reduced by NDGA, an inhibitor of the lipoxygenase-cytochrome P450 mono-oxygenase system, suggesting that metabolism of arachidonic acid through this pathway is required for the induction of c-jun mRNA by oxidants. Both hydrogen peroxide and arachidonic acid significantly increased c-jun transcription as demonstrated by nuclear run-on assays. Together these observations suggest that: (1) the induction of c-jun mRNA by hydrogen peroxide is mediated by PLA2-dependent arachidonic acid release and metabolism through the lipoxygenase-cytochrome P450 mono-oxygenase system; (2) PKC appears to be involved in this signaling pathway and (3) the induction of c-jun mRNA by hydrogen peroxide in RASM cells is due to increased transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acid / pharmacology*
  • Cells, Cultured
  • Down-Regulation
  • Glyceraldehyde-3-Phosphate Dehydrogenases / metabolism
  • Hydrogen Peroxide / pharmacology*
  • Male
  • Masoprocol / pharmacology
  • Muscle, Smooth, Vascular / metabolism*
  • Peptide Fragments / metabolism
  • Phospholipases A / pharmacology
  • Phospholipases A2
  • Protein Kinase C / metabolism
  • Proto-Oncogene Proteins c-jun / metabolism*
  • Quinacrine / pharmacology
  • RNA, Messenger / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Transcription, Genetic / drug effects*

Substances

  • Peptide Fragments
  • Proto-Oncogene Proteins c-jun
  • RNA, Messenger
  • glyceraldehyde 3-phosphate dehydrogenase (304-313)
  • Arachidonic Acid
  • Masoprocol
  • Hydrogen Peroxide
  • Glyceraldehyde-3-Phosphate Dehydrogenases
  • Protein Kinase C
  • Phospholipases A
  • Phospholipases A2
  • Quinacrine