Effect of diesel exhaust particles on human middle ear epithelial cells

Int J Pediatr Otorhinolaryngol. 2012 Mar;76(3):334-8. doi: 10.1016/j.ijporl.2011.12.003. Epub 2011 Dec 29.

Abstract

Objective: In the present study, we investigate whether diesel exhaust particles (DEPs) cause cytotoxicity and induce inflammation or increase the expression of mucin in immortalized human middle ear epithelial cell lines (HMEECs). Several publications have shown an association between traffic-related air pollutants and otitis media. Additionally, DEP have been shown to cause inflammation and an allergic response in the airways.

Methods: Cell viability following DEP treatment was investigated in HMEECs using the MTT assay. We measured the expression of the inflammatory cytokines TNF-α and COX-2 and the mucin genes MUC5AC and MUC5B using semiquantitative real-time reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting.

Results: Cell viability tests showed that exposure to more than 80 μg/mL of DEP caused a decrease in cell viability. DEP exposure also increased the expression of MUC5AC, but did not induce the expression of MUC5B in HMEECs.

Conclusion: DEP decreased cell viability, induced an inflammatory response, and increased mucin gene expression in HMEECs. These findings support the hypothesis that environmental diesel exposure is a risk factor for otitis media.

MeSH terms

  • Air Pollutants / pharmacology*
  • Cell Culture Techniques
  • Cell Line
  • Cell Survival / drug effects
  • Cyclooxygenase 2 / metabolism
  • Ear, Middle / drug effects*
  • Ear, Middle / metabolism
  • Ear, Middle / pathology*
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Humans
  • Mucin 5AC / metabolism
  • Mucin-5B / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Vehicle Emissions / toxicity*

Substances

  • Air Pollutants
  • MUC5AC protein, human
  • MUC5B protein, human
  • Mucin 5AC
  • Mucin-5B
  • Tumor Necrosis Factor-alpha
  • Vehicle Emissions
  • Cyclooxygenase 2