Glucocorticoids suppress group II phospholipase A2 production by blocking mRNA synthesis and post-transcriptional expression

J Biol Chem. 1990 Jul 25;265(21):12745-8.

Abstract

We investigated the effects of glucocorticoids on group II phospholipase A2 (PLA2) expression in rat cultured smooth muscle cells. Both forskolin-induced and tumor necrosis factor (TNF)-induced PLA2 release responses were almost completely blocked by 10 and 100 nM dexamethasone, respectively, as assayed by protein blotting and PLA2 activity assays. Dexamethasone-mediated inhibition of PLA2 release appeared to be mediated by the glucocorticoid receptor. Dexamethasone at concentrations greater than 10 nM inhibited forskolin-induced elevation of the group II PLA2 mRNA level but not TNF-induced elevation. These data suggest that the mechanism mediating forskolin-induced mRNA accumulation is sensitive to glucocorticoids, but the mechanism mediating the TNF-induced accumulation is not. Inhibition of TNF-induced PLA2 release by glucocorticoids may be explained by the blocking of post-transcriptional synthesis of the group II PLA2.

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Colforsin / pharmacology
  • Dexamethasone / pharmacology
  • Gene Expression / drug effects
  • Glucocorticoids / pharmacology*
  • In Vitro Techniques
  • Inflammation / enzymology
  • Muscle, Smooth, Vascular / physiology
  • Phospholipases / genetics*
  • Phospholipases A / biosynthesis
  • Phospholipases A / genetics*
  • Phospholipases A2
  • Progesterone / pharmacology
  • RNA Processing, Post-Transcriptional / drug effects
  • RNA, Messenger / genetics
  • Rats
  • Rats, Inbred Strains
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Glucocorticoids
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Colforsin
  • Progesterone
  • Dexamethasone
  • Phospholipases
  • Phospholipases A
  • Phospholipases A2