Oxacyclododecindione, a novel inhibitor of IL-4 signaling from Exserohilum rostratum

J Antibiot (Tokyo). 2008 May;61(5):285-90. doi: 10.1038/ja.2008.40.

Abstract

In a screening program for new metabolites from fungi inhibiting the IL-4 mediated signal transduction, a novel chlorinated macrocyclic lactone, designated as oxacyclododecindione, was isolated from fermentations of the imperfect fungus Exserohilum rostratum. The structure was determined by a combination of spectroscopic techniques. Oxacyclododecindione inhibits the IL-4 induced expression of the reporter gene secreted alkaline phosphatase (SEAP) in transiently transfected HepG2 cells with IC50 values of 20-25 ng/ml (54-67.5 nM). Studies on the mode of action of the compound revealed that the inhibition of the IL-4 dependent signaling pathway is caused by blocking the binding of the activated STAT6 transcription factors to the DNA binding site without inhibiting tyrosine phosphorylation. The compound has no antibacterial or antifungal activity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blotting, Western
  • Cell Line, Tumor
  • Fermentation
  • Gene Expression / drug effects
  • Humans
  • Interleukin-4 / antagonists & inhibitors*
  • Interleukin-4 / pharmacology
  • Interleukin-4 / physiology*
  • Macrocyclic Compounds / chemistry*
  • Macrocyclic Compounds / pharmacology*
  • Magnetic Resonance Spectroscopy
  • Mitosporic Fungi / chemistry*
  • Mitosporic Fungi / metabolism
  • STAT6 Transcription Factor / antagonists & inhibitors
  • STAT6 Transcription Factor / physiology
  • Signal Transduction / drug effects
  • Spectrometry, Mass, Electrospray Ionization
  • Structure-Activity Relationship
  • Transfection

Substances

  • Macrocyclic Compounds
  • STAT6 Transcription Factor
  • oxacyclododecindione
  • Interleukin-4