N-acetylcysteine attenuates TNF-alpha-dependent reduction of IL-4-induced Fc epsilon RII expression in human monocytes

Allergy. 1997 Sep;52(9):909-13. doi: 10.1111/j.1398-9995.1997.tb01250.x.

Abstract

We have previously shown that tumor necrosis factor-alpha (TNF-alpha) reduces interleukin-4 (IL-4)-induced Fc epsilon RII expression in human monocytes. It has been shown that TNF-alpha activates nuclear transcriptional factors through the generation of reactive oxygen intermediates (ROIs), and antioxidant N-acetylcysteine (NAC) inhibits TNF-alpha-induced activation of nuclear transcriptional factors. Therefore, we hypothesized that TNF-alpha-dependent reduction of IL-4-induced Fc epsilon RII expression in monocytes might be mediated through the ROIs-activated mechanism. In the present study, to test our hypothesis, we examined the effect of NAC on TNF-alpha-dependent reduction of IL-4-induced Fc epsilon RII expression in human monocytes. NAC attenuated TNF-alpha-dependent reduction of IL-4-induced Fc epsilon RII expression by attenuating TNF-alpha-dependent reduction of Fc epsilon RII mRNA expression. Similarly, the structurally unrelated antioxidant, pyrrolidine dithiocarbamate (PDTC), also effectively attenuated this-reduction. These results indicate that an ROIs-activated and antioxidant-sensitive mechanism might be involved in TNF-alpha-dependent reduction of IL-4-induced Fc epsilon RII expression in monocytes.

MeSH terms

  • Acetylcysteine / pharmacology*
  • Antioxidants / pharmacology
  • Cells, Cultured
  • Free Radical Scavengers / pharmacology*
  • Humans
  • Interleukin-4 / immunology*
  • Monocytes / drug effects*
  • Monocytes / immunology
  • Pyrrolidines / pharmacology
  • Receptors, IgE / analysis*
  • Receptors, IgE / drug effects*
  • Receptors, IgE / genetics
  • Thiocarbamates / pharmacology
  • Tumor Necrosis Factor-alpha / drug effects*
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Antioxidants
  • Free Radical Scavengers
  • Pyrrolidines
  • Receptors, IgE
  • Thiocarbamates
  • Tumor Necrosis Factor-alpha
  • Interleukin-4
  • pyrrolidine dithiocarbamic acid
  • Acetylcysteine