Genotoxicity of fine and coarse fraction ambient particulate matter in immortalised normal (TT1) and cancer‐derived (A549) alveolar epithelial cells

• Published in: Environmental and molecular mutagenesis 2018-05, Vol.59 (4), p.290-301
• Main Authors: Jarvis, Ian W.H., Enlo‐Scott, Zachary, Nagy, Eszter, Mudway, Ian S., Tetley, Teresa D., Arlt, Volker M., Phillips, David H., Gollapudi, B.
• Format: Article
• Language: English
• Subjects: A549 Cells; air pollution; Airborne particulates; Alveolar Epithelial Cells - drug effects; alveolar epithelium; Alveoli; Benzo(a)pyrene; Cancer; Carcinogens; Cell Line; DNA Damage; DNA damage response; Enzyme-Linked Immunosorbent Assay; Epithelial cells; Exposure; Genotoxicity; Health risks; Humans; Lung cancer; Lungs; Mutagenesis; Mutagenicity Tests; Particle Size; Particulate emissions; Particulate matter; Particulate Matter - toxicity; Particulates; Polycyclic aromatic hydrocarbons; Polycyclic Aromatic Hydrocarbons - toxicity; Pyrene; Toxicity; Transition metals; Tumor cell lines; Tumors
• ISSN: 0893-6692; 1098-2280
• DOI: 10.1002/em.22166

Human exposure to airborne particulate matter (PM) is associated with adverse cardiopulmonary health effects, including lung cancer. Ambient PM represents a heterogeneous mixture of chemical classes including transition metals, polycyclic aromatic hydrocarbons (PAHs) and their derivatives such as nitro‐PAHs, many of which are classified as putative carcinogens. As the primary site of human exposure to PM is the lungs, we investigated the response of two alveolar epithelial cell lines, the tumour‐derived A549 and newly described TT1 cells, to fine and coarse PM collected from background and roadside locations. We show that coarse PM elicits a genotoxic response in the TT1 cells, with the strongest signal associated with the background sample. This response could be recapitulated using the organic extract derived from this sample. No responses were observed in PM‐challenged A549 cells. Fine PM failed to elicit a genotoxic response in either cell line despite the higher PAH concentrations within this fraction. Consistent with the lack of a simplistic association between PM PAH content and the observed genotoxic response, TT1 cells treated with benzo[a]pyrene (BaP) demonstrated no increase in the selected markers. In contrast, a pattern of response was observed in TT1 cells challenged with 3‐nitrobenzanthrone (3‐NBA) similar to that with coarse PM. Together, these data illustrated the suitability of the TT1 cell line for assessing PM‐induced genotoxicity and challenge the contention that fine roadside PM poses the higher cancer risk. Furthermore, the response to 3‐NBA and not BaP suggests a major contribution of nitro‐PAHs to the overall toxicity of PM. Environ. Mol. Mutagen. 59:290–301, 2018. © 2018 The Authors Environmental and Molecular Mutagenesis published by Wiley Periodicals, Inc. on behalf of Environmental Mutagen Society