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Global Gene Expression Profiling of Human Lung Epithelial Cells After Exposure to Nanosilver
Author(s) -
Rasmus Foldbjerg,
Eveline S. Irving,
Yuya Hayashi,
Duncan S. Sutherland,
Kasper Thorsen,
Herman Autrup,
Christiane Beer
Publication year - 2012
Publication title -
toxicological sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.352
H-Index - 183
eISSN - 1096-6080
pISSN - 1096-0929
DOI - 10.1093/toxsci/kfs225
Subject(s) - silver nanoparticle , gene expression , cell cycle , flow cytometry , a549 cell , transcriptome , heat shock protein , microbiology and biotechnology , gene expression profiling , microarray analysis techniques , reactive oxygen species , gene , chemistry , downregulation and upregulation , nanotoxicology , cell culture , apoptosis , biology , biochemistry , toxicity , materials science , genetics , organic chemistry , nanoparticle , nanotechnology
The toxic effects of silver nanoparticles (AgNPs) on cells are well established, but only limited studies on the effect of AgNPs and silver ions on the cellular transcriptome have been performed. In this study, the effect of AgNPs on the gene expression in the human lung epithelial cell line A549 exposed to 12.1 µg/ml AgNPs (EC20) for 24 and 48h was compared with the response to control and silver ion (Ag(+)) treated cells (1.3 µg/ml) using microarray analysis. Twenty-four hours to AgNP altered the regulation of more than 1000 genes (more than twofold regulation), whereas considerably fewer genes responded to Ag(+) (133 genes). The upregulated genes included members of the metallothionein, heat shock protein, and histone families. As expected from the induction of meta l lothionein and heat shock protein genes, Ag(+) and AgNP treatment resulted in intracellular production of reactive oxygen species but did not induce apoptosis or necrosis at the concentrations used in this study. In addition, the exposure to AgNPs influenced the cell cycle and led to an arrest in the G2/M phase as shown by cell cycle studies by flow cytometry and microscopy. In conclusion, although the transcriptional response to Ag(+) exposure was highly related to the response caused by AgNPs, our findings suggest that AgNPs, due to their particulate form, affect exposed cells in a more complex way.

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