Post-transcriptional regulation of LTC4 synthase activity by retinoic acid in rat basophilic leukemia cells

Biochim Biophys Acta. 1997 Aug 16;1347(2-3):205-11. doi: 10.1016/s0005-2760(97)00076-3.

Abstract

Calcium ionophore-stimulated production of leukotriene (LT) C4 was enhanced by 16- to 26-h incubation with retinoic acid (RA) in rat basophilic leukemia-1 cells. Production of LTC4 by enzyme assay using cell lysates as the enzyme source and LTA4 as the substrate was also enhanced by RA-treatment. Production of LTB4 was not enhanced under these two experimental conditions, suggesting the preferential activation of LTC4 synthase activity. The RA-induced enhancement of LTC4 synthesis by the cells was suppressed by co-incubation with dexamethasone (DEX) or cyclosporine A (CSA). However, the expression of mRNA for LTC4 synthase was not affected by the exposure to RA, DEX or CSA. These results indicate that RA-induced enhancement of LTC4 production and its inhibition by DEX and CSA was determined by post-transcriptional regulation of LTC4 synthase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcimycin / pharmacology
  • Cyclosporine / pharmacology
  • Dexamethasone / pharmacology
  • Drug Synergism
  • Enzyme Activation
  • Glutathione Transferase / antagonists & inhibitors
  • Glutathione Transferase / metabolism*
  • Leukotriene C4 / biosynthesis
  • Leukotriene C4 / genetics
  • RNA, Messenger / analysis
  • Rats
  • Tretinoin / pharmacology*
  • Tumor Cells, Cultured / drug effects

Substances

  • RNA, Messenger
  • Leukotriene C4
  • Calcimycin
  • Tretinoin
  • Dexamethasone
  • Cyclosporine
  • Glutathione Transferase
  • leukotriene-C4 synthase