Proinflammatory effects of diesel exhaust particles from moderate blend concentrations of 1st and 2nd generation biodiesel in BEAS-2B bronchial epithelial cells-The FuelHealth project

Environ Toxicol Pharmacol. 2017 Jun:52:138-142. doi: 10.1016/j.etap.2017.04.004. Epub 2017 Apr 5.

Abstract

Biodiesel fuel fuels are introduced at an increasing extent as a more carbon-neutral alternative to reduce CO2-emissions, compared to conventional diesel fuel. In the present study we have investigated the impact of increasing the use of 1st generation fatty acid methyl ester (FAME) biodiesel from current 7% blend (B7) to 20% blend (B20), or by increasing the biodiesel content by adding 2nd generation hydrotreated vegetable oil (HVO) based biodiesel (SHB; Synthetic Hydrocarbon Biofuel) on toxicity of diesel exhaust particles (DEP) in an in vitro system. Human bronchial epithelial BEAS-2B cells were exposed for 4 and 20h to DEP from B7, B20 and SHB at different concentrations, and examined for effects on gene expression of interleukin 6 (IL-6), CXCL8 (IL-8), CYP1A1 and heme oxygenase-1 (HO-1). The results show that both B20 and SHB were more potent inducers of IL-6 expression compared to B7. Only B20 induced statistically significant increases in CXCL8 expression. By comparison the rank order of potency to induce CYP1A1 was SHB>B7>B20. No statistically significant difference were observed form HO-1 expression, suggesting that the differences in cytokine responses were not due to oxidative stress. The results show that even moderate increases in biodiesel blends, from 7% to 20%, may increase the proinflammatory potential of emitted DEP in BEAS-2B cells. This effect was observed for both addition of 1st generation FAME and 2nd generation HVO biodiesel.

Keywords: Air pollution; Biodiesel; Cytokines; Inflammation; Lung cells; Oxidative stress; Particulate matter.

MeSH terms

  • Air Pollutants / toxicity*
  • Biofuels*
  • Bronchi / cytology
  • Cell Line
  • Cytochrome P-450 CYP1A1 / genetics
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Gene Expression / drug effects
  • Heme Oxygenase-1 / genetics
  • Humans
  • Interleukin-6 / genetics
  • Interleukin-8 / genetics
  • Particulate Matter / toxicity*
  • Vehicle Emissions / toxicity*

Substances

  • Air Pollutants
  • Biofuels
  • CXCL8 protein, human
  • IL6 protein, human
  • Interleukin-6
  • Interleukin-8
  • Particulate Matter
  • Vehicle Emissions
  • CYP1A1 protein, human
  • Cytochrome P-450 CYP1A1
  • HMOX1 protein, human
  • Heme Oxygenase-1