Characteristics and cellular effects of ambient particulate matter from Beijing

Environ Pollut. 2014 Aug:191:63-9. doi: 10.1016/j.envpol.2014.04.008. Epub 2014 May 8.

Abstract

In vitro tests using human adenocarcinomic alveolar epithelial cell line A549 and small mouse monocyte-macrophage cell line J774A.1 were conducted to test toxicity of six PM (particulate matter) samples from Beijing. The properties of the samples differ significantly. The production of inflammatory cytokine (TNF-α for J774A.1) and chemokine (IL-8 for A549) and the level of intracellular reactive oxygen species (ROS) were used as endpoints. There was a positive correlation between water soluble organic carbon and DTT-based redox activity. Both cell types produced increased levels of inflammatory mediators and had higher level of intracelllar ROS, indicating the presence of PM-induced inflammatory response and oxidative stress, which were dose-dependent and significantly different among the samples. The releases of IL-8 from A549 and TNF-α from J774A.1 were significantly correlated to PM size, Zeta potential, endotoxin, major metals, and polycyclic aromatic hydrocarbons. No correlation between ROS and these properties was identified.

Keywords: Cytotoxicity; Inflammatory effect; In vitro test; Particulate matter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Endotoxins / analysis
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Humans
  • Interleukin-8 / metabolism
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Metals / analysis
  • Mice
  • Oxidation-Reduction
  • Oxidative Stress / drug effects
  • Particulate Matter / chemistry
  • Particulate Matter / toxicity*
  • Polycyclic Aromatic Hydrocarbons / analysis
  • Reactive Oxygen Species / metabolism
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Endotoxins
  • Interleukin-8
  • Metals
  • Particulate Matter
  • Polycyclic Aromatic Hydrocarbons
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha