Toxicity of nano- and ionic silver to embryonic stem cells: a comparative toxicogenomic study

被引:37
|
作者
Gao, Xiugong [1 ]
Topping, Vanessa D. [1 ]
Keltner, Zachary [1 ]
Sprando, Robert L. [1 ]
Yourick, Jeffrey J. [1 ]
机构
[1] US FDA, Div Appl Regulatory Toxicol, Off Appl Res & Safety Assessment, Ctr Food Safety & Appl Nutr, 8301 Muirkirk Rd, Laurel, MD 20708 USA
关键词
Silver nanoparticles; Silver ion; Embryonic stem cell; Developmental toxicity; Transcriptomics; DEVELOPMENTAL TOXICITY; ORAL TOXICITY; NANOPARTICLES; EXPRESSION; GENOTOXICITY; METALLOTHIONEIN; DIFFERENTIATION; CYTOTOXICITY; TRANSLOCATION; RESPONSES;
D O I
10.1186/s12951-017-0265-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The widespread application of silver nanoparticles (AgNPs) and silver-containing products has raised public safety concerns about their adverse effects on human health and the environment. To date, in vitro toxic effects of AgNPs and ionic silver (Ag+) on many somatic cell types are well established. However, no studies have been conducted hitherto to evaluate their effect on cellular transcriptome in embryonic stem cells (ESCs). Results: The present study characterized transcriptomic changes induced by 5.0 mu g/ml AgNPs during spontaneous differentiation of mouse ESCs, and compared them to those induced by Ag+ under identical conditions. After 24 h exposure, 101 differentially expressed genes (DEGs) were identified in AgNP-treated cells, whereas 400 genes responded to Ag+. Despite the large differences in the numbers of DEGs, functional annotation and pathway analysis of the regulated genes revealed overall similarities between AgNPs and Ag+. In both cases, most of the functions and pathways impacted fell into two major categories, embryonic development and metabolism. Nevertheless, a number of canonical pathways related to cancer were found for Ag+ but not for AgNPs. Conversely, it was noted that several members of the heat shock protein and the metallothionein families were upregulated by AgNPs but not Ag+, suggesting specific oxidative stress effect of AgNPs in ESCs. The effects of AgNPs on oxidative stress and downstream apoptosis were subsequently confirmed by flow cytometry analysis. Conclusions: Taken together, the results presented in the current study demonstrate that both AgNPs and Ag+ caused transcriptomic changes that could potentially exert an adverse effect on development. Although transcriptomic responses to AgNPs and Ag+ were substantially similar, AgNPs exerted specific effects on ESCs due to their nanosized particulate form.
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页数:18
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