TY - JOUR
T1 - Diesel exhaust particles are mutagenic in FE1-Muta™Mouse lung epithelial cells
AU - Jacobsen, Nicklas Raun
AU - Møller, Peter
AU - Cohn, Corey Alexander
AU - Loft, Steffen
AU - Vogel, Ulla Birgitte
AU - Wallin, Håkan
PY - 2008
Y1 - 2008
N2 - The particulate phase of diesel engine exhaust is likely carcinogenic. However, the mechanisms of diesel exhaust particles (DEPs) induced mutagenicity/carcinogenicity are still largely unknown. We determined the mutant frequency following eight repeated 72 h incubations with 37.5 or 75 mu g/ml DEP (NIST SRM 1650) in the FE1-Muta(TM)Mouse lung epithelial cell line. We measured DEP-induced acellular and intracellular production of reactive oxygen species (ROS) and compared with ROS production induced by carbon black, which WE, have previously shown is mutagenic in this cell line [N.R. Jacobsen, A.T. Saber, P. White, P. Moller, G. Pojana, U. Vogel, S. Loft, J.Gingerich, L. Soper, G.R. Douglas, H. Wallin. Increased mutant frequency by carbon black,, but not quartz, in the lacZ and cII transgenes of muta(TM)mouse lung epithelial cells, Environ. Mol. Mutagen. 48(6) (2007) 451-461]. The mutant frequency was marginally elevated in cells treated with 37.5 mu g/ml DEP (1.29-fold [95% CI: 0.96-1.601, p = 0.08) and significantly increased in cells treated with 75 mu g/ml DEP (1.55-fold [95% CI: 1.23-1.871, p <0.001). ROS production from DEP was low both within cells and in acellular systems when compared to carbon black. These results show that DEP are mutagenic in a mammalian cell line in vitro and that additional pathways besides ROS production, such as those involving the presence of polycyclic aromatic hydrocarbons, likely are involved in the mutagenesis. (C) 2008 Elsevier B.V. All rights reserved.
AB - The particulate phase of diesel engine exhaust is likely carcinogenic. However, the mechanisms of diesel exhaust particles (DEPs) induced mutagenicity/carcinogenicity are still largely unknown. We determined the mutant frequency following eight repeated 72 h incubations with 37.5 or 75 mu g/ml DEP (NIST SRM 1650) in the FE1-Muta(TM)Mouse lung epithelial cell line. We measured DEP-induced acellular and intracellular production of reactive oxygen species (ROS) and compared with ROS production induced by carbon black, which WE, have previously shown is mutagenic in this cell line [N.R. Jacobsen, A.T. Saber, P. White, P. Moller, G. Pojana, U. Vogel, S. Loft, J.Gingerich, L. Soper, G.R. Douglas, H. Wallin. Increased mutant frequency by carbon black,, but not quartz, in the lacZ and cII transgenes of muta(TM)mouse lung epithelial cells, Environ. Mol. Mutagen. 48(6) (2007) 451-461]. The mutant frequency was marginally elevated in cells treated with 37.5 mu g/ml DEP (1.29-fold [95% CI: 0.96-1.601, p = 0.08) and significantly increased in cells treated with 75 mu g/ml DEP (1.55-fold [95% CI: 1.23-1.871, p <0.001). ROS production from DEP was low both within cells and in acellular systems when compared to carbon black. These results show that DEP are mutagenic in a mammalian cell line in vitro and that additional pathways besides ROS production, such as those involving the presence of polycyclic aromatic hydrocarbons, likely are involved in the mutagenesis. (C) 2008 Elsevier B.V. All rights reserved.
U2 - 10.1016/j.mrfmmm.2008.03.001
DO - 10.1016/j.mrfmmm.2008.03.001
M3 - Journal article
C2 - 18423769
SN - 0027-5107
VL - 641
JO - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
JF - Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis
IS - 1-2
ER -