Activation of the aryl hydrocarbon receptor is the major toxic mode of action of an organic extract of a reference urban dust particulate matter mixture: the role of polycyclic aromatic hydrocarbons
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
P42ES016465
NIEHS NIH HHS - United States
PubMed
21762708
DOI
10.1016/j.mrfmmm.2011.06.011
PII: S0027-5107(11)00153-9
Knihovny.cz E-resources
- MeSH
- DNA Adducts drug effects MeSH
- Apoptosis drug effects MeSH
- Cell Line MeSH
- Cytochrome P-450 CYP1A1 metabolism MeSH
- Genes, p53 drug effects MeSH
- Liver drug effects MeSH
- Rats MeSH
- Mutagens toxicity MeSH
- Organic Chemicals toxicity MeSH
- Particulate Matter toxicity MeSH
- Polycyclic Aromatic Hydrocarbons toxicity MeSH
- DNA Damage drug effects MeSH
- Cell Proliferation drug effects MeSH
- Receptors, Aryl Hydrocarbon metabolism MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- DNA Adducts MeSH
- Cytochrome P-450 CYP1A1 MeSH
- Mutagens MeSH
- Organic Chemicals MeSH
- Particulate Matter MeSH
- Polycyclic Aromatic Hydrocarbons MeSH
- Receptors, Aryl Hydrocarbon MeSH
Many of the toxic and carcinogenic effects of urban air pollution have been linked to polycyclic aromatic hydrocarbons (PAHs) adsorbed to airborne particulate matter (PM). The carcinogenic properties of PAHs in complex organic mixtures derived from PM have been chiefly attributed to their mutagenicity. Nevertheless, PAHs are also potent activators of the aryl hydrocarbon receptor (AhR), which may contribute to their nongenotoxic effects, including tumor promotion. As the genotoxicity of carcinogenic PAHs in complex mixtures derived from urban PM is often inhibited by other mixture constituents, the AhR-mediated activity of urban PM extracts might significantly contribute to the carcinogenic activity of such mixtures. In the present study, we used an organic extract of the urban dust standard reference material, SRM1649a, as a model mixture to study a range of toxic effects related to DNA damage and AhR activation. Both the organic extract and its neutral aromatic fraction formed a low number of DNA adducts per nucleotide in the liver epithelial WB-F344 cells model, without inducing DNA damage response, such as tumor suppressor p53 activation and apoptosis. In contrast, we found that this extract, as well as its neutral and polar fractions, were potent inducers of a range of AhR-mediated responses, including induction of the AhR-mediated transcription, such as cytochrome P450 1A1/1B1 expression, and the AhR-dependent cell proliferation. Importantly, these toxic events occurred at doses one order of magnitude lower than DNA damage. The AhR-mediated activity of the neutral fraction was linked to PAHs and their derivatives, as polychlorinated dibenzo-p-dioxins, dibenzofurans and biphenyls were only minor contributors to the overall AhR-mediated activity. Taken together, our data suggest that more attention should be paid to the AhR-dependent nongenotoxic events elicited by urban PM constituents, especially PAHs and their derivatives.
Department of Cytokinetics Institute of Biophysics AS CR Královopolská 135 61265 Brno Czech Republic
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