Silver nanoparticles induced changes in the expression of NF-κB related genes are cell type specific and related to the basal activity of NF-κB.
| Title: | Silver nanoparticles induced changes in the expression of NF-κB related genes are cell type specific and related to the basal activity of NF-κB. |
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| Authors: | Stępkowski TM; Institute of Nuclear Chemistry and Technology, Centre for Radiobiology and Biological Dosimetry, Dorodna 16, 03-195 Warsaw, Poland. Electronic address: t.stepkowski@ichtj.waw.pl.; Brzóska K; Institute of Nuclear Chemistry and Technology, Centre for Radiobiology and Biological Dosimetry, Dorodna 16, 03-195 Warsaw, Poland. Electronic address: k.brzoska@ichtj.waw.pl.; Kruszewski M; Institute of Nuclear Chemistry and Technology, Centre for Radiobiology and Biological Dosimetry, Dorodna 16, 03-195 Warsaw, Poland; Institute of Agricultural Medicine, Department of Molecular Biology and Translational Research, Jaczewskiego 2, 20-090 Lublin, Poland. Electronic address: m.kruszewski@ichtj.waw.pl. |
| Source: | Toxicology in vitro : an international journal published in association with BIBRA [Toxicol In Vitro] 2014 Jun; Vol. 28 (4), pp. 473-8. Date of Electronic Publication: 2014 Jan 23. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Language: | English |
| Journal Info: | Publisher: Pergamon Press Country of Publication: England NLM ID: 8712158 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-3177 (Electronic) Linking ISSN: 08872333 NLM ISO Abbreviation: Toxicol In Vitro Subsets: MEDLINE |
| Imprint Name(s): | Original Publication: Oxford ; New York : Pergamon Press, c1987- |
| MeSH Terms: | Gene Expression Regulation/*drug effects ; Metal Nanoparticles/*toxicity ; NF-kappa B/*metabolism ; Silver/*toxicity; Metal Nanoparticles/chemistry ; NF-kappa B/genetics ; Silver/chemistry ; Cell Line, Tumor ; Humans ; Signal Transduction |
| Abstract: | Silver nanoparticles (AgNPs) are widely used in industry and medicine but the recent evidence for their cytotoxicity rise a concern about the safety of their use. We have previously shown that human A549 cells are resistant to AgNPs cytotoxicity, as compared with similarly treated HepG2 cells. In order to check for the role of the NF-κB signaling pathway in response of A549 and HepG2 cell lines to the treatment with 20 nm and 200 nm AgNps, we analyzed the expression of 84 key genes related to the functionality of the NF-κB signaling pathway. We observed considerable alternations in gene expression in HepG2 cells treated with 20 nm AgNPs, and minor changes when exposed to 200 nm AgNPs. Surprisingly, no changes in gene expression were observed in A549 cells treated with both size AgNPs. Using the NF-κB luciferase reporter system, we further tested the basal activity and inducibility of the NF-κB pathway in both cell lines and found that the inducibility of NF-κB signaling in A549 cells is approximately 5 times lower than this of HepG2 cells, but the basal activity is approximately 3.5 times higher. In accordance, the NF-κB activation after AgNPs treatment was observed in HepG2 but not in A549. Altogether indicate that NF-kB mediated cellular response to AgNPs is cell type specific and related to the basal activity of NF-κB.; (Copyright © 2014 Elsevier Ltd. All rights reserved.) |
| Contributed Indexing: | Keywords: Cell signaling; Gene expression; Luciferase; Nanotoxicology; Reporter assay |
| Substance Nomenclature: | 0 (NF-kappa B); 3M4G523W1G (Silver) |
| Entry Date(s): | Date Created: 20140128 Date Completed: 20150629 Latest Revision: 20140331 |
| Update Code: | 20260130 |
| DOI: | 10.1016/j.tiv.2014.01.008 |
| PMID: | 24462830 |
| Database: | MEDLINE |
Journal Article; Research Support, Non-U.S. Gov't