Analysis of gene expression changes in A549 cells induced by organic compounds from respirable air particles
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25771875
DOI
10.1016/j.mrfmmm.2014.10.002
PII: S0027-5107(14)00184-5
Knihovny.cz E-zdroje
- Klíčová slova
- A549 cells, Ah receptor, Gene expression profile, PAHs, PM2.5,
- MeSH
- adenokarcinom plic MeSH
- adenokarcinom genetika patologie MeSH
- exprese genu účinky léků MeSH
- lidé MeSH
- mikročipová analýza MeSH
- nádorové buňky kultivované MeSH
- nádory plic genetika patologie MeSH
- organické látky farmakologie MeSH
- pevné částice farmakologie MeSH
- regulace genové exprese u nádorů účinky léků MeSH
- respirační sliznice účinky léků metabolismus MeSH
- signální transdukce účinky léků genetika MeSH
- stanovení celkové genové exprese MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- organické látky MeSH
- pevné částice MeSH
A number of toxic effects of respirable ambient air particles (genotoxic effects, inflammation, oxidative damage) have been attributed to organic compounds bound onto the particle surface. In this study, we analyzed global gene expression changes caused by the extractable organic matters (EOMs) from respirable airborne particles <2.5μm (PM2.5), collected at 3 localities from heavily polluted areas of the Czech Republic and a control locality with low pollution levels, in human lung epithelial A549 cells. Although the sampled localities differed in both extent and sources of air pollution, EOMs did not induce substantially different gene expression profiles. The number of transcripts deregulated in A549 cells treated with the lowest EOM concentration (10μg/ml) ranged from 65 to 85 in 4 sampling localities compared to the number of transcripts deregulated after 30μg/ml and 60μg/ml of EOMs, which ranged from 90 to 109, and from 149 to 452, respectively. We found numerous commonly deregulated genes and pathways related to activation of the aryl hydrocarbon receptor (AhR) and metabolism of xenobiotics and endogenous compounds. We further identified deregulation of expression of the genes involved in pro-inflammatory processes, oxidative stress response and in cancer and developmental pathways, such as TGF-β and Wnt signaling pathways. No cell cycle arrest, DNA repair or pro-apoptotic responses were identified at the transcriptional level after the treatment of A549 cells with EOMs. In conclusion, numerous processes and pathways deregulated in response to EOMs suggest a significant role of activated AhR. Interestingly, we did not observe substantial gene expression changes related to DNA damage response, possibly due to the antagonistic effect of non-genotoxic EOM components. Moreover, a comparison of EOM effects with other available data on modulation of global gene expression suggests possible overlap among the effects of PM2.5, EOMs and various types of AhR agonists.
Czech Technical University Prague Karlovo namesti 13 121 35 Prague 2 Czech Republic
Veterinary Research Institute Hudcova 296 70 621 00 Brno Czech Republic
Citace poskytuje Crossref.org
