Brefeldin A reduces tumor necrosis factor-α-stimulated production of inflammatory mediators by suppressing the Akt, mTOR, and NF-κB pathways in human keratinocytes

Naunyn Schmiedebergs Arch Pharmacol. 2016 Sep;389(9):951-60. doi: 10.1007/s00210-016-1242-6. Epub 2016 May 20.

Abstract

Keratinocytes may play an important role in the pathogenesis of inflammatory skin diseases. Brefeldin A has been shown to attenuate the production and secretion of chemical mediators involved in inflammation and immune responses. However, the effect of brefeldin A on the TNF-α-stimulated production of inflammatory mediators in keratinocytes has not been studied. We investigated the effect of brefeldin A on the TNF-α-stimulated production of inflammatory mediators using HaCaT cells and primary keratinocytes in relation to the Akt, mTOR, and NF-κB pathways, which regulates the transcription genes involved in immune and inflammatory responses. Brefeldin A, Akt inhibitor, Bay 11-7085 (an inhibitor of NF-κB activation), and rapamycin (mTOR inhibitor) inhibited the TNF-α-stimulated productions of inflammatory mediators, and activations of Akt, mTOR, and NF-κB in keratinocytes. The results show that brefeldin A appears to attenuate TNF-α-stimulated inflammatory mediator production in keratinocytes by suppressing the activation of the Akt, mTOR, and NF-κB pathways.

Keywords: Akt, mTOR, and NF-κB pathways; Brefeldin A; Inflammatory mediator production; Keratinocytes; Tumor necrosis factor-α.

MeSH terms

  • Anti-Inflammatory Agents / pharmacology*
  • Brefeldin A / pharmacology*
  • Cell Line
  • Cell Survival / drug effects
  • Dermatitis / enzymology
  • Dermatitis / prevention & control*
  • Dose-Response Relationship, Drug
  • Humans
  • Inflammation Mediators / metabolism*
  • Keratinocytes / drug effects*
  • Keratinocytes / enzymology
  • Keratinocytes / pathology
  • NF-kappa B / antagonists & inhibitors
  • NF-kappa B / metabolism*
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction / drug effects
  • TOR Serine-Threonine Kinases / antagonists & inhibitors
  • TOR Serine-Threonine Kinases / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Anti-Inflammatory Agents
  • Inflammation Mediators
  • NF-kappa B
  • Protein Kinase Inhibitors
  • Tumor Necrosis Factor-alpha
  • Brefeldin A
  • MTOR protein, human
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases