A role of cellular glutathione in the differential effects of iron oxide nanoparticles on antigen-specific T cell cytokine expression

Int J Nanomedicine. 2011:6:2791-8. doi: 10.2147/IJN.S25588. Epub 2011 Nov 8.

Abstract

Background: Accumulating evidence indicates that iron oxide nanoparticles modulate immune responses, and induce oxidative stress in macrophages. It was recently reported that iron oxide nanoparticles attenuated antigen-specific immunity in vivo, though the underlying mechanism remains elusive. The present study investigates the direct effect of iron oxide nanoparticles on antigen-specific cytokine expression by T cells, and potential underlying mechanisms.

Methods: Ovalbumin-primed splenocytes were exposed to iron oxide nanoparticles, followed by restimulation with ovalbumin. Cell viability, cytokine production, and cellular levels of glutathione and reactive oxygen species were measured.

Results: The splenocyte viability and the production of interleukin-2 and interleukin-4 were unaffected, whereas interferon-γ production was markedly attenuated by iron oxide nanoparticles (10-100 μg iron/mL) in a concentration-dependent manner. Iron oxide nanoparticles also transiently diminished the intracellular level of glutathione, with a peak response at 6 hours posttreatment. The effects of iron oxide nanoparticles on interferon-γ and glutathione were attenuated by the presence of N-acetyl-L-cysteine, a precursor of glutathione. However, iron oxide nanoparticles did not influence the generation of reactive oxygen species.

Conclusion: Iron oxide nanoparticles induced a differential effect on antigen-specific cytokine expression by T cells, in which the T helper 1 cytokine IFN-γ was sensitive, whereas the T helper 2 cytokine interleukin-4 was refractory. In addition, the suppressive effect of iron oxide nanoparticles on interferon-γ was closely associated with the diminishment of glutathione.

Keywords: T cell; antigen-specific; cytokine; glutathione; iron oxide nanoparticle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Cell Survival / drug effects
  • Cytokines / biosynthesis*
  • Ferric Compounds / chemistry
  • Ferric Compounds / pharmacology*
  • Glutathione / metabolism*
  • Interferon-gamma / biosynthesis
  • Interleukins / biosynthesis
  • Magnetite Nanoparticles / chemistry*
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Ovalbumin
  • Reactive Oxygen Species / metabolism
  • Spleen / cytology
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / metabolism

Substances

  • Antioxidants
  • Cytokines
  • Ferric Compounds
  • Interleukins
  • Magnetite Nanoparticles
  • Reactive Oxygen Species
  • ferric oxide
  • Interferon-gamma
  • Ovalbumin
  • Glutathione