Cellular uptake, intracellular trafficking and cytotoxicity of silver nanoparticles

被引:246
|
作者
Singh, Raman Preet [1 ]
Ramarao, Poduri [1 ]
机构
[1] Natl Inst Pharmaceut Educ & Res, Dept Pharmacol & Toxicol, Sas Nagar 160062, Punjab, India
关键词
Silver nanoparticles; Silver ions; Mitochondria; Cellular uptake; Toxicity; WALLED CARBON NANOTUBES; IN-VITRO TOXICITY; CROSS-PRESENTATION; ACCUMULATION; MECHANISMS; MEMBRANE; EXPOSURE; EFFICACY; DELIVERY; RELEASE;
D O I
10.1016/j.toxlet.2012.07.009
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Silver nanoparticles (Ag NPs) are used in consumer products and wound dressings due to their antimicrobial properties. However, in addition to toxic effects on microbes, Ag NPs can also induce stress responses as well as cytotoxicity in mammalian cells. We observed that Ag NPs are efficiently internalized via scavenger receptor-mediated phagocytosis in murine macrophages. Confocal and electron microscopy analysis revealed that internalized Ag NPs localize in the cytoplasm. Ag NPs cause mitochondrial damage, induce apoptosis and cell death. These effects were abrogated in presence of Ag ion-reactive, thiol-containing compounds suggesting the central of Ag ions in Ag NP toxicity. Quantitative image analysis revealed that intracellular dissolution of Ag NPs occurs about 50 times faster than in water. In conclusion, we demonstrate for the first time that Ag NPs are internalized by scavenger receptors, trafficked to cytoplasm and induce toxicity by releasing Ag ions. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:249 / 259
页数:11
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