Hypothemycin inhibits tumor necrosis factor-α production by tristetraprolin-dependent down-regulation of mRNA stability in lipopolysaccharide-stimulated macrophages

Int Immunopharmacol. 2015 Dec;29(2):863-868. doi: 10.1016/j.intimp.2015.08.030. Epub 2015 Sep 12.

Abstract

Hypothemycin, a resorcylic acid lactone polyketide, has been shown to inhibit oncogenic ras-transformation and T cell activation. In the present study, we investigated the effect of hypothemycin on tumor necrosis factor-α (TNF-α) production in macrophages and the molecular mechanisms involved in this effect. Hypothemycin potently suppressed the TNF-α production without affecting nitric oxide production in lipopolysaccharide (LPS)-stimulated macrophages. However, hypothemycin had no effect on the activity of TNF-α-converting enzyme, a key enzyme for converting membrane-bound pro-TNF-α into soluble TNF-α. Further study demonstrated that the stability of TNF-α mRNA was decreased by hypothemycin treatment. In addition, hypothemycin suppressed LPS-induced phosphorylation of p38 MAPK and ERK. Moreover, knockdown of tristetraprolin (TTP), which is an important trans-acting regulator of TNF-α mRNA stability and downstream target of p38 MAPK and ERK, reversed hypothemycin-mediated inhibition of TNF-α mRNA expression. Collectively, our results suggest that hypothemycin suppresses TNF-α production by TTP-dependent destabilization of TNF-α mRNA and this is mediated, at least in part, by blocking the activation of p38 MAPK and ERK.

Keywords: Hypothemycin; Tristetraprolin; Tumor necrosis factor-α; mRNA stability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADAM Proteins / drug effects
  • ADAM Proteins / metabolism
  • ADAM17 Protein
  • Animals
  • Down-Regulation / drug effects
  • Humans
  • Lipopolysaccharides / pharmacology*
  • Macrophages / drug effects
  • Macrophages / metabolism*
  • Mice
  • Nitric Oxide / biosynthesis
  • RAW 264.7 Cells
  • RNA Stability / drug effects*
  • Tristetraprolin / pharmacology*
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / biosynthesis*
  • Zearalenone / analogs & derivatives*
  • Zearalenone / pharmacology
  • p38 Mitogen-Activated Protein Kinases / antagonists & inhibitors

Substances

  • Lipopolysaccharides
  • Tristetraprolin
  • Tumor Necrosis Factor-alpha
  • hypothemycin
  • Nitric Oxide
  • Zearalenone
  • p38 Mitogen-Activated Protein Kinases
  • ADAM Proteins
  • ADAM17 Protein