Cerium dioxide nanoparticles can interfere with the associated cellular mechanistic response to diesel exhaust exposure

Toxicol Lett. 2012 Oct 17;214(2):218-25. doi: 10.1016/j.toxlet.2012.08.026. Epub 2012 Sep 6.

Abstract

The aim of this study was to compare the biological response of a sophisticated in vitro 3D co-culture model of the epithelial airway barrier to a co-exposure of CeO(2) NPs and diesel exhaust using a realistic air-liquid exposure system. Independent of the individual effects of either diesel exhaust or CeO(2) NPs investigation observed that a combined exposure of CeO(2) NPs and diesel exhaust did not cause a significant cytotoxic effect or alter cellular morphology after exposure to diesel exhaust for 2h at 20μg/ml (low dose) or for 6h at 60μg/ml (high dose), and a subsequent 6h exposure to an aerosolized solution of CeO(2) NPs at the same doses. A significant loss in the reduced intracellular glutathione level was recorded, although a significant increase in the oxidative marker HMOX-1 was found after exposure to a low and high dose respectively. Both the gene expression and protein release of tumour necrosis factor-α were significantly elevated after a high dose exposure only. In conclusion, CeO(2) NPs, in combination with diesel exhaust, can significantly interfere with the cell machinery, indicating a specific, potentially adverse role of CeO(2) NPs in regards to the biological response of diesel exhaust exposure.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Survival / drug effects
  • Cerium / pharmacology*
  • Coculture Techniques
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Glutathione / metabolism
  • Heme Oxygenase-1 / genetics
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Microscopy, Fluorescence
  • Nanoparticles / administration & dosage*
  • Oxidative Stress / drug effects*
  • Oxidative Stress / physiology
  • RNA / chemistry
  • RNA / genetics
  • Real-Time Polymerase Chain Reaction
  • Respiratory System / drug effects*
  • Respiratory System / metabolism
  • Superoxide Dismutase / genetics
  • Superoxide Dismutase / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Vehicle Emissions / toxicity*

Substances

  • Tumor Necrosis Factor-alpha
  • Vehicle Emissions
  • Cerium
  • ceric oxide
  • RNA
  • HMOX1 protein, human
  • Heme Oxygenase-1
  • Superoxide Dismutase
  • Glutathione