Responsiveness assessment of a 3D tetra-culture alveolar model exposed to diesel exhaust particulate matter

Toxicol In Vitro. 2018 Dec:53:67-79. doi: 10.1016/j.tiv.2018.07.019. Epub 2018 Aug 3.

Abstract

The aim of the current study was to evaluate the responses of a 3D tetra-culture alveolar model cultivated at the air-liquid-interface (ALI) after apical exposure to diesel exhaust particulate matter (DEPM) based on the three-tiered oxidative stress concept. The alveolar model exposed to increasing doses of DEPM (1.75-5 μg/cm2) responded with increasing activity of the anti-oxidant defense mechanisms (Nrf2 translocation, increased gene expression for anti-oxidant proteins and increased HMOX-1 synthesis) (tier 1). Higher exposure generated a proinflammatory response (NF-kB translocation, increased gene expression of pro-inflammatory cytokines and adhesion molecules, and increased IL-6 and IL-8 synthesis) (tier 2) and, finally, the highest doses applied resulted in a decrease of cell viability due to necrosis (extra-cellular release of LDH) or apoptosis (increased expression of the pro-apoptotic genes CASP7 and FAS) (tier 3). Overall, the results of our study demonstrate that the 3D tetra-culture model when directly exposed to DEPM potently generates a realistic response according to the three-tiered oxidative stress concept. Further evaluation and benchmarking against currently used in vivo rodent models is needed to show its suitability, and to serve in the future as an alternative for in vivo studies in the hazard evaluation of inhalable irritants.

Keywords: Air-liquid exposure; Diesel exhaust particulate matter; Inflammation; Oxidative stress; Tetra-culture.

MeSH terms

  • Air Pollutants / toxicity*
  • Apoptosis / drug effects
  • Cell Culture Techniques
  • Cell Line
  • Cell Survival / drug effects
  • Gene Expression / drug effects
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Membrane Proteins / metabolism
  • Necrosis / chemically induced
  • Particulate Matter / toxicity*
  • Pulmonary Alveoli*
  • Vehicle Emissions / toxicity*

Substances

  • Air Pollutants
  • CXCL8 protein, human
  • IL6 protein, human
  • Interleukin-6
  • Interleukin-8
  • Membrane Proteins
  • Particulate Matter
  • Vehicle Emissions
  • Heme Oxygenase-1
  • Hmox1 protein, mouse