2008
DOI: 10.1016/j.tox.2007.11.016
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Gene expression induction of volatile organic compound and/or polycyclic aromatic hydrocarbon-metabolizing enzymes in isolated human alveolar macrophages in response to airborne particulate matter (PM2.5)

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Cited by 45 publications
(30 citation statements)
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“…A recent study has demonstrated that PAH coated onto PM 2.5 could induce gene expression of cyto-chrome P450 (CYP) 1A1, CYP2E1, NADPH quinone oxydo-reductase-1, and glutathione S -transferasepi 1 and mu 3 in human alveolar macrophages, suggesting the formation of biologically reactive metabolites and the role of carbonaceous core of PM as a physical carrier (Saint-Georges et al 2008). Quinones act as catalysts that produce ROS and may be key compounds in PM toxicity along with transition metals.…”
Section: Discussionmentioning
confidence: 99%
“…A recent study has demonstrated that PAH coated onto PM 2.5 could induce gene expression of cyto-chrome P450 (CYP) 1A1, CYP2E1, NADPH quinone oxydo-reductase-1, and glutathione S -transferasepi 1 and mu 3 in human alveolar macrophages, suggesting the formation of biologically reactive metabolites and the role of carbonaceous core of PM as a physical carrier (Saint-Georges et al 2008). Quinones act as catalysts that produce ROS and may be key compounds in PM toxicity along with transition metals.…”
Section: Discussionmentioning
confidence: 99%
“…Organic chemical compounds such as oxy-PAHs and quinones are relevant organic chemical species in terms of PM redox chemistry and ROS generation (Bonvallot et al 2001;Cho et al 2005;Kumagai et al 1997;Monks et al 1992;Penning et al 1999). A recent study has demonstrated that PAH coated onto PM 2.5 could induce gene expression of cytochrome P450 (CYP) 1A1, CYP2E1, NADPH quinone oxydo-reductase-1, and glutathione S-transferase-pi 1 and mu 3 in human alveolar macrophages, suggesting the formation of biologically reactive metabolites and the role of carbonaceous core of PM as a physical carrier (Saint-Georges et al 2008). Quinones act as catalysts that produce ROS and may be key compounds in PM toxicity along with transition metals.…”
Section: Discussionmentioning
confidence: 99%
“…Increases in Cyp2e1 mRNA expression were observed in human alveolar epithelial carcinoma-derived cell line (A549) and in human alveolar macrophages incubated with fine particles (PM2.5) isolated from ambient air in the industrial area of the city of Dunkerque (France). It was suggested that volatile organic compounds (VOC; e.g., benzene, toluene, xylene), and polycyclic aromatic hydrocarbons (PAH; e.g., anthracene, phenanthrene, pyrene) both constituents of particulate air pollutants are responsible for the increased expression of Cyp2e1 in cell cultures (Billet et al 2007;Saint-Georges et al 2008). Cyp2e1 was also reported to be constitutively expressed in rat cardiomyocyte cultures, was found in all regions of human hearts and its expression was up-regulated in rat hearts exposed to benzo-α-pyrene (one of the PAHs identified in ambient PM) (Thum and Borlak 2000a;Thum and Borlak 2000b;Saint-Georges et al 2008;Aboutabl et al 2009).…”
Section: Discussionmentioning
confidence: 99%
“…Once in the remote organ, volatile organic compounds (VOC) and PAH can up-regulate the expression of Cyp2e1 and undergo oxidative Phase I metabolism. Oxidation of VOC and PAH by the cytochrome P450 monooxygenase system could yield highly reactive epoxy compounds with increased toxic potentials (Billet et al 2007;Saint-Georges et al 2008). However, following phase I oxidation, activated foreign substances undergo Phase II reactions catalyzed primarily by glutathione-S-transferase.…”
Section: Discussionmentioning
confidence: 99%