Toxicology Reports · 2015 · 79 citations · 26 references
Life SciencesCell BiologyToxicologyApoptosisMolecular ImagingNanomaterialsCell-nanoparticle InteractionsNanomedicineNanotoxicologyOxidative Damage To BiomoleculesReactive Oxygen SpeciesReactive Oxygen Species BiologyApoptosis Induction By NanoparticlesCell Viability AssaysLive-cell ImagingNanoparticle ToxicityNanoparticle-induced CytotoxicityReactive Oxygen Species GenerationReactive Oxygen Species InjuryTemporal Expression
• Exposing cells to nanosilver particles (AgNPs) immediately induces ROS. • Smaller AgNPs induce mitochondrial ROS production. • AgNP-induced mitochondrial ROS are independent of particle internalisation. Silver nanoparticles (AgNPs) induce the production of reactive oxygen species (ROS) and apoptosis. These effects are enhanced by smaller particles. Using live-cell imaging, we show that AgNPs induced ROS production rapidly in a size-dependent manner after exposure of cells to 70-nm and 1-nm AgNPs (AgNPs-70, AgNPs-1), but not AgNO 3 . Exposure of cells to 5 μg/mL each of AgNPs-70, AgNPs-1 or AgNO 3 for 1 h decreased the cell viability by approximately 40%, 100% and 20%, respectively. ROS were rapidly induced after 5 and 60 min by AgNPs-1 and AgNPs-70, respectively, whereas AgNO 3 had no detectable effect. ROS production detected using the reporter dichlorodihydrofluorescein was observed in whole cells and mitochondria 5 and 60 min after exposure to AgNPs-1. The present study is the first, to our knowledge, to report the temporal expression and intracellular localisation of ROS induced by AgNPs.
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