Effects of silver nanoparticles on human and rat embryonic neural stem cells

被引:77
|
作者
Liu, Fang [1 ]
Mahmood, Meena [2 ]
Xu, Yang [2 ]
Watanabe, Fumiya [2 ]
Biris, Alexandru S. [2 ]
Hansen, Deborah K. [3 ]
Inselman, Amy [3 ]
Casciano, Daniel [2 ]
Patterson, Tucker A. [1 ]
Paule, Merle G. [1 ]
Slikker, William, Jr. [1 ]
Wang, Cheng [1 ]
机构
[1] US FDA, Natl Ctr Toxicol Res, Div Neurotoxicol, Food & Drug Adm, Jefferson, AR 72079 USA
[2] Univ Arkansas, Ctr Integrat Nanotechnol Sci, Little Rock, AR 72204 USA
[3] US FDA, Natl Ctr Toxicol Res, Div Syst Biol, Food & Drug Adm, Jefferson, AR 72079 USA
来源
FRONTIERS IN NEUROSCIENCE | 2015年 / 9卷
关键词
silver nanoparticles; neural stem cells; developmental neurotoxicity; reactive oxygen species; acetyl-l-carnitine; ACETYL-L-CARNITINE; HUMAN SKIN KERATINOCYTES; D-ASPARTATE RECEPTOR; OXIDATIVE STRESS; ALZHEIMERS-DISEASE; FOREBRAIN CULTURE; INDUCED APOPTOSIS; CARBON NANOTUBES; CORTICAL-NEURONS; SPINAL-CORD;
D O I
10.3389/fnins.2015.00115
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Silver nano-particles (Ag-NPs) are becoming increasingly prevalent in consumer products as antibacterial agents. The increased use of Ag NP-enhanced products will almost certainly increase environmental silver levels, resulting in increased exposures and the potential for increased adverse reactions including neurotoxic effects. In the present study, embryonic neural stem cells (NSCs) from human and rat fetuses (gestational day-16) were used to determine whether Ag-NPs are capable of causing developmental neurotoxicity. The NSCs were cultured in serum free medium supplemented with appropriate growth factors. On the eighth day in vitro (DIV 8), the cells were exposed to Ag-NPs at concentrations of 1, 5, 10, and 20 mu g/ml for 24h. The cultured cells then were characterized by NSC markers including nestin and SOX2 and a variety of assays were utilized to determine the effects of Ag-NPs on NSC proliferation and viability and the underlying mechanisms associated with these effects. The results indicate that mitochondrial viability (MTT metabolism) was substantially attenuated and LDH release was increased significantly in a dose-dependent manner. Ag-NPs-induced neurotoxicity was further confirmed by up-regulated Bax protein expression, an increased number of TUN EL-positively stained cells, and elevated reactive oxygen species (ROS). NSC proliferation was also significantly decreased by Ag-NPs. Co-administration of acetyl-L-carnitine, an antioxidant agent, effectively blocked the adverse effects associated with Ag-NP exposure.
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页数:9
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