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Global gene expression changes in human embryonic lung fibroblasts induced by organic extracts from respirable air particles
H. Líbalová, K. Uhlířová, J. Kléma, M. Machala, RJ. Šrám, M. Ciganek, J. Topinka,
Language English Country England, Great Britain
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
BioMedCentral
from 2004-01-12
BioMedCentral Open Access
from 2004
Directory of Open Access Journals
from 2004
Free Medical Journals
from 2004
PubMed Central
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from 2009-01-01
Open Access Digital Library
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Open Access Digital Library
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from 2004-12-01
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from 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2004
Springer Nature OA/Free Journals
from 2004-12-01
PubMed
22239852
DOI
10.1186/1743-8977-9-1
Knihovny.cz E-resources
- MeSH
- Gene Expression drug effects MeSH
- Fibroblasts cytology drug effects physiology MeSH
- Air Pollutants chemistry metabolism pharmacology MeSH
- Humans MeSH
- Microarray Analysis MeSH
- Organic Chemicals chemistry metabolism pharmacology MeSH
- Oxidation-Reduction MeSH
- Particulate Matter chemistry metabolism pharmacology MeSH
- Lung cytology MeSH
- Gene Expression Profiling MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Geographicals
- Czech Republic MeSH
BACKGROUND: Recently, we used cell-free assays to demonstrate the toxic effects of complex mixtures of organic extracts from urban air particles (PM2.5) collected in four localities of the Czech Republic (Ostrava-Bartovice, Ostrava-Poruba, Karvina and Trebon) which differed in the extent and sources of air pollution. To obtain further insight into the biological mechanisms of action of the extractable organic matter (EOM) from ambient air particles, human embryonic lung fibroblasts (HEL12469) were treated with the same four EOMs to assess changes in the genome-wide expression profiles compared to DMSO treated controls. METHOD: For this purpose, HEL cells were incubated with subtoxic EOM concentrations of 10, 30, and 60 μg EOM/ml for 24 hours and global gene expression changes were analyzed using human whole genome microarrays (Illumina). The expression of selected genes was verified by quantitative real-time PCR. RESULTS: Dose-dependent increases in the number of significantly deregulated transcripts as well as dose-response relationships in the levels of individual transcripts were observed. The transcriptomic data did not differ substantially between the localities, suggesting that the air pollution originating mainly from various sources may have similar biological effects. This was further confirmed by the analysis of deregulated pathways and by identification of the most contributing gene modulations. The number of significantly deregulated KEGG pathways, as identified by Goeman's global test, varied, depending on the locality, between 12 to 29. The Metabolism of xenobiotics by cytochrome P450 exhibited the strongest upregulation in all 4 localities and CYP1B1 had a major contribution to the upregulation of this pathway. Other important deregulated pathways in all 4 localities were ABC transporters (involved in the translocation of exogenous and endogenous metabolites across membranes and DNA repair), the Wnt and TGF-β signaling pathways (associated particularly with tumor promotion and progression), Steroid hormone biosynthesis (involved in the endocrine-disrupting activity of chemicals), and Glycerolipid metabolism (pathways involving the lipids with a glycerol backbone including lipid signaling molecules). CONCLUSION: The microarray data suggested a prominent role of activation of aryl hydrocarbon receptor-dependent gene expression.
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