Mechanistic study on the biological effects of silver and gold nanoparticles in Caco-2 cells - Induction of the Nrf2/HO-1 pathway by high concentrations of silver nanoparticles

被引:97
作者
Aueviriyavit, Sasitorn [1 ]
Phummiratch, Duangkamol [1 ]
Maniratanachote, Rawiwan [1 ]
机构
[1] NSTDA, Natl Nanotechnol Ctr, Nano Safety & Risk Assessment Lab, Pathum Thani 12120, Thailand
关键词
Silver nanoparticles; Gold nanoparticles; Nrf2; Heme oxygenase-1; Gastrointestinal system; Caco-2; cells; HEME OXYGENASE-1; OXIDATIVE STRESS; NANO-SILVER; TOXICITY; NRF2; CYTOTOXICITY; NANOSILVER; RESPONSES; PRODUCTS; INJURY;
D O I
10.1016/j.toxlet.2013.09.020
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The most commonly used metal nanoparticles (NPs) across diverse applications, including in agro-food applications, include silver (AgNPs) and gold (AuNPs). In the present study, we aimed to investigate the biological responses and possible toxicological effects of AgNPs and AuNPs in the Caco-2 cells as an in vitro human GI tract model. Both AgNPs and AuNPs were internalized into the cytoplasm of Caco-2 cells, but not within the nucleus and only exposure to high concentrations of AgNPs, but not AuNPs, caused acute cytotoxicity and depolarization of the mitochondrial membrane potential. In addition, only AgNPs significantly depleted the total intracellular glutathione level, induced the activation of the stress-responsive gene, Nrf2, and dramatically increased the expression of heme oxygenase-1 (HO-1). Furthermore, siRNA silencing of Nrf2 transcripts significantly reduced the AgNP-induced HO-1 mRNA induction, suggesting a key role for Nrf2 in the control of HO-1 expression. Taken together, AgNPs but not AuNPs induced acute cytotoxicity and cellular responses via the oxidative stress-related activation of Nrf2HO-1 signaling pathway in Caco-2 cells. The expression of HO-1 transcripts may be useful as a sensitive marker for safety evaluation of AgNPs in the GI tract of humans. Crown Copyright (C) 2013 Published by Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:73 / 83
页数:11
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