Cytokine and chemokine expression patterns in lung epithelial cells exposed to components characteristic of particulate air pollution

Toxicology. 2009 May 2;259(1-2):46-53. doi: 10.1016/j.tox.2009.01.028. Epub 2009 Feb 12.

Abstract

Airborne particulate matter (PM) has a complex composition, and the relative contribution of different compounds to PM-induced effects is only partly understood. The present study compared the capability of selected components commonly found in PM, to induce pro-inflammatory responses in lung epithelial cells. Ultrafine carbon black (ufCB), ZnCl(2), FeSO(4), 1-nitropyrene (1-NP), lipopolysaccharide (LPS), and crystalline silica (positive control) were screened for effects on the expression of 84 inflammation-related genes in the bronchial epithelial cell line, BEAS-2B. A total of 22 genes were up-regulated by one or more of the tested compounds, and 5 cytokine and 11 chemokine genes were selected for further studies. After 10h exposure, silica induced significantly increased expression of CCL20, CXCL1/-3/-8/-10/-11, lymphotoxin (LT)beta and interleukin (IL)-6; ufCB induced CXCL8/-10 and -11; ZnCl(2) induced CCL11/-20/-26, CXCL1/-5/-8/-14 and tumor necrosis factor (TNF)-alpha; FeSO(4) induced a weak up-regulation of CXCL8 and TNF-alpha; LPS induced CCL20, CXCL1/-5/-8/-10/-11, LTbeta and IL-6; and 1-NP induced expression of CCL20, CXCL1/-3/-8, TNF-alpha and IL-6. Despite obvious differences, all compounds induced response-patterns that correlated relatively well with that of silica, the positive control. The predominant response appeared to be increased gene expression of neutrophil-recruiting CXC-chemokines. CXCL8 was the only gene induced by all tested PM-components, the most up-regulated on average, and also dominating the gene-expression patterns induced by coarse PM. The data show quantitative, and to a certain extent qualitative differences in cytokine/chemokine gene-expression profiles of the compounds tested. However, there were also striking similarities in the response-patterns induced by these physically/chemically widely different compounds.

Publication types

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

MeSH terms

  • Air Pollutants / chemistry
  • Air Pollutants / toxicity*
  • Bronchi / cytology
  • Bronchi / drug effects
  • Bronchi / metabolism
  • Cell Line, Transformed
  • Cell Line, Tumor
  • Chemokines / drug effects*
  • Chemokines / genetics
  • Chemokines / metabolism
  • Cytokines / drug effects*
  • Cytokines / genetics
  • Cytokines / metabolism
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Humans
  • Lung / cytology
  • Lung / drug effects
  • Lung / metabolism
  • Lung Neoplasms / metabolism
  • Neutrophils / drug effects
  • Neutrophils / metabolism
  • Silicon Dioxide / toxicity
  • Up-Regulation / drug effects*

Substances

  • Air Pollutants
  • Chemokines
  • Cytokines
  • Silicon Dioxide