Nejvíce citovaný článek - PubMed ID 22239852
Global gene expression changes in human embryonic lung fibroblasts induced by organic extracts from respirable air particles
Nitrated monoaromatic hydrocarbons (NMAHs) are ubiquitous in the environment and an important part of atmospheric humic-like substances (HULIS) and brown carbon. They are ecotoxic and with underresearched toxic potential for humans. NMAHs were determined in size-segregated ambient particulate matter collected at two urban sites in central Europe, Ostrava and Kladno, Czech Republic. The average sums of 12 NMAHs (Σ12NMAH) measured in winter PM10 samples from Ostrava and Kladno were 102 and 93 ng m-3, respectively, and 8.8 ng m-3 in summer PM10 samples from Ostrava. The concentrations in winter corresponded to 6.3-7.3% and 2.6-3.1% of HULIS-C and water-soluble organic carbon (WSOC), respectively. Nitrocatechols represented 67-93%, 61-73% and 28-96% of NMAHs in PM10 samples collected in winter and summer at Ostrava and in winter at Kladno, respectively. The mass size distribution of the targeted substance classes peaked in the submicrometre size fractions (PM1), often in the PM0.5 size fraction especially in summer. The bioaccessible fraction of NMAHs was determined by leaching PM3 samples in two simulated lung fluids, Gamble's solution and artificial lysosomal fluid (ALF). More than half of NMAH mass is found bioaccessible, almost complete for nitrosalicylic acids. The bioaccessible fraction was generally higher when using ALF (mimics the chemical environment created by macrophage activity, pH 4.5) than Gamble's solution (pH 7.4). Bioaccessibility may be negligible for lipophilic substances (i.e. log KOW > 4.5).
- Klíčová slova
- Aerosol, Air pollution, Bioaccessibility, Nitroaromatic compounds,
- MeSH
- dusičnany MeSH
- dusíkaté sloučeniny MeSH
- katecholy MeSH
- látky znečišťující vzduch * analýza MeSH
- lidé MeSH
- monitorování životního prostředí MeSH
- nitrofenoly MeSH
- pevné částice * analýza MeSH
- toluen MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- dusičnany MeSH
- dusíkaté sloučeniny MeSH
- katecholy MeSH
- látky znečišťující vzduch * MeSH
- nitrocatechol MeSH Prohlížeč
- nitrofenoly MeSH
- pevné částice * MeSH
- toluen MeSH
Among the nitrated and oxygenated polycyclic aromatic hydrocarbons (NPAHs and OPAHs) are some of the most hazardous substances to public health, mainly because of their carcinogenicity and oxidative potential. Despite these concerns, the concentrations and fate of NPAHs and OPAHs in the atmospheric environment are largely unknown. Ambient air concentrations of 18 NPAHs, 5 quinones, and 5 other OPAHs were determined at two urban and one regional background sites in central Europe. At one of the urban sites, the total (gas and particulate) concentrations of Σ10OPAHs were 10.0 ± 9.2 ng/m3 in winter and 3.5 ± 1.6 ng/m3 in summer. The gradient to the regional background site exceeded 1 order of magnitude. Σ18NPAH concentrations were typically 1 order of magnitude lower than OPAHs. Among OPAHs, 9-fluorenone and (9,10)-anthraquinone were the most abundant species, accompanied by benzanthrone in winter. (9,10)-Anthraquinone represented two-thirds of quinones. We found that a large fraction of the target substance particulate mass was carried by submicrometer particles. The derived inhalation bioaccessibility in the PM10 size fraction is found to be ≈5% of the total ambient concentration of OPAHs and up to ≈2% for NPAHs. For 9-fluorenone and (9,10)-anthraquinone, up to 86 and 18%, respectively, were found at the rural site. Our results indicate that water solubility could function as a limiting factor for bioaccessibility of inhaled particulate NPAHs and OPAHs, without considerable effect of surfactant lipids and proteins in the lung lining fluid.
- MeSH
- dusičnany MeSH
- látky znečišťující vzduch * MeSH
- lidé MeSH
- monitorování životního prostředí MeSH
- pevné částice MeSH
- polycyklické aromatické uhlovodíky * MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Geografické názvy
- Evropa MeSH
- Názvy látek
- dusičnany MeSH
- látky znečišťující vzduch * MeSH
- pevné částice MeSH
- polycyklické aromatické uhlovodíky * MeSH
The cellular response to genotoxic treatment depends on the cell line used. Although tumor cell lines are widely used for genotoxicity tests, the interpretation of the results may be potentially hampered by changes in cellular processes caused by malignant transformation. In our study we used normal human embryonic lung fibroblasts (HEL12469 cells) and tested their response to treatment with benzo[a]pyrene (B[a]P) and extractable organic matter (EOM) from ambient air particles <2.5 µm (PM2.5) collected in two Czech cities differing in levels and sources of air pollution. We analyzed multiple endpoints associated with exposure to polycyclic aromatic hydrocarbons (PAHs) including the levels of bulky DNA adducts and the nucleotide excision repair (NER) response [expression of XPE, XPC and XPA genes on the level of mRNA and proteins, unscheduled DNA synthesis (UDS)]. EOMs were collected in the winter and summer of 2011 in two Czech cities with different levels and sources of air pollution. The effects of the studied compounds were analyzed in the presence (+S9) and absence (-S9) of the rat liver microsomal S9 fraction. The levels of bulky DNA adducts were highest after treatment with B[a]P, followed by winter EOMs; their induction by summer EOMs was weak. The induction of both mRNA and protein expression was observed, with the most pronounced effects after treatment with B[a]P (-S9); the response induced by EOMs from both cities and seasons was substantially weaker. The expression of DNA repair genes was not accompanied by the induction of UDS activity. In summary, our results indicate that the tested compounds induced low levels of DNA damage and affected the expression of NER genes; however, nucleotide excision repair was not induced.
- MeSH
- adukty DNA MeSH
- buněčné linie MeSH
- DNA vazebné proteiny genetika metabolismus MeSH
- fibroblasty účinky léků metabolismus MeSH
- látky znečišťující vzduch chemie toxicita MeSH
- látky znečišťující životní prostředí chemie toxicita MeSH
- lidé MeSH
- messenger RNA genetika MeSH
- oprava DNA * MeSH
- pevné částice chemie toxicita MeSH
- plíce MeSH
- polycyklické aromatické uhlovodíky chemie toxicita MeSH
- proliferace buněk účinky léků MeSH
- regulace genové exprese účinky léků MeSH
- xeroderma pigmentosum - protein skupiny A genetika metabolismus MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adukty DNA MeSH
- DNA vazebné proteiny MeSH
- látky znečišťující vzduch MeSH
- látky znečišťující životní prostředí MeSH
- messenger RNA MeSH
- pevné částice MeSH
- polycyklické aromatické uhlovodíky MeSH
- xeroderma pigmentosum - protein skupiny A MeSH
- XPA protein, human MeSH Prohlížeč
- XPC protein, human MeSH Prohlížeč