| Literature DB >> 22960666 |
Sandro Steiner1, Loretta Mueller, Olga B Popovicheva, David O Raemy, Jan Czerwinski, Pierre Comte, Andreas Mayer, Peter Gehr, Barbara Rothen-Rutishauser, Martin J D Clift.
Abstract
The aim of this study was to compare the biological response of a sophisticated in vitro 3D co-culture model of the epithelial airway barrier to a co-exposure of CeO(2) NPs and diesel exhaust using a realistic air-liquid exposure system. Independent of the individual effects of either diesel exhaust or CeO(2) NPs investigation observed that a combined exposure of CeO(2) NPs and diesel exhaust did not cause a significant cytotoxic effect or alter cellular morphology after exposure to diesel exhaust for 2h at 20μg/ml (low dose) or for 6h at 60μg/ml (high dose), and a subsequent 6h exposure to an aerosolized solution of CeO(2) NPs at the same doses. A significant loss in the reduced intracellular glutathione level was recorded, although a significant increase in the oxidative marker HMOX-1 was found after exposure to a low and high dose respectively. Both the gene expression and protein release of tumour necrosis factor-α were significantly elevated after a high dose exposure only. In conclusion, CeO(2) NPs, in combination with diesel exhaust, can significantly interfere with the cell machinery, indicating a specific, potentially adverse role of CeO(2) NPs in regards to the biological response of diesel exhaust exposure.Entities:
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Year: 2012 PMID: 22960666 DOI: 10.1016/j.toxlet.2012.08.026
Source DB: PubMed Journal: Toxicol Lett ISSN: 0378-4274 Impact factor: 4.372