Nonhomologous DNA end joining and chromosome aberrations in human embryonic lung fibroblasts treated with environmental pollutants
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
24694657
DOI
10.1016/j.mrfmmm.2014.03.006
PII: S0027-5107(14)00053-0
Knihovny.cz E-resources
- Keywords
- Benzo[a]pyrene, Chromosome aberrations, Double-strand DNA breaks, Extractable organic matter, Nonhomologous DNA end joining repair,
- MeSH
- Ku Autoantigen MeSH
- Antigens, Nuclear genetics metabolism MeSH
- Benzo(a)pyrene toxicity MeSH
- Cell Line MeSH
- DNA-Binding Proteins genetics metabolism MeSH
- Embryo, Mammalian metabolism pathology MeSH
- Fibroblasts metabolism pathology MeSH
- Phosphorylation drug effects genetics MeSH
- Histones genetics metabolism MeSH
- Environmental Pollutants toxicity MeSH
- Humans MeSH
- Chromosomes, Human genetics metabolism MeSH
- Urban Renewal MeSH
- DNA End-Joining Repair drug effects genetics MeSH
- Particulate Matter MeSH
- Lung metabolism pathology MeSH
- Translocation, Genetic drug effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
- Names of Substances
- Ku Autoantigen MeSH
- Antigens, Nuclear MeSH
- Benzo(a)pyrene MeSH
- DNA-Binding Proteins MeSH
- H2AX protein, human MeSH Browser
- Histones MeSH
- Environmental Pollutants MeSH
- Particulate Matter MeSH
- XRCC4 protein, human MeSH Browser
- Xrcc6 protein, human MeSH Browser
In order to evaluate the ability of a representative polycyclic aromatic hydrocarbon (PAH) and PAH-containing complex mixtures to induce double strand DNA breaks (DSBs) and repair of damaged DNA in human embryonic lung fibroblasts (HEL12469 cells), we investigated the effect of benzo[a]pyrene (B[a]P) and extractable organic matter (EOM) from ambient air particles <2.5μm (PM2.5) on nonhomologous DNA end joining (NHEJ) and induction of stable chromosome aberrations (CAs). PM2.5 was collected in winter and summer 2011 in two Czech cities differing in levels and sources of air pollutants. The cells were treated for 24h with the following concentrations of tested chemicals: B[a]P: 1μM, 10μM, 25μM; EOMs: 1μg/ml, 10μg/ml, 25μg/ml. We tested several endpoints representing key steps leading from DSBs to the formation of CAs including histone H2AX phosphorylation, levels of proteins Ku70, Ku80 and XRCC4 participating in NHEJ, in vitro ligation activity of nuclear extracts of the HEL12469 cells and the frequency of stable CAs assessed by whole chromosome painting of chromosomes 1, 2, 4, 5, 7 and 17 using fluorescence in situ hybridization. Our results show that 25μM of B[a]P and most of the tested doses of EOMs induced DSBs as indicated by H2AX phosphorylation. DNA damage was accompanied by induction of XRCC4 expression and an increased frequency of CAs. Translocations most frequently affected chromosome 7. We observed only a weak induction of Ku70/80 expression as well as ligation activity of nuclear extracts. In summary, our data suggest the induction of DSBs and NHEJ after treatment of human embryonic lung fibroblasts with B[a]P and complex mixtures containing PAHs.
References provided by Crossref.org
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