The Journal of Toxicological Sciences · 2013 · 38 citations · 16 references
Life SciencesBiochemistryToxicologyApoptosisDna RepairNanomaterialsGenotoxicity MechanismsGenotoxicity TestingMetal ToxicityNanotoxicologyOxidative Damage To BiomoleculesReactive Oxygen SpeciesDna Double-strand BreaksDouble-strand Dna BreaksGenotoxicityHistone H2ax PhosphorylationNanoparticle CytotoxicityNanoparticle GenotoxicityNanoparticle ToxicityNanoparticle-induced Cytotoxicity
We examined the genotoxicity of magnetite nanoparticles (primary particle size: 10 nm) on human A549 and Chinese hamster ovary (CHO) AA8 cells. Six hours' treatment with the particles dose-dependently increased the frequency of micronuclei (MN) in the A549 and CHO AA8 cells up to 5.2% and 5.0% at a dose of 200 µg/ml (34 µg/cm²), respectively. In A549 cells, treatment with the nano-particles (2 µg/ml) for 1 hr induced H2AX phosphorylation, which is suggestive of DNA double strand breaks (DSB). Treating CHO AA8 cells with 2 µg/ml (0.34 µg/cm²) magnetite for 1 hour resulted in a five times higher frequency of sister chromatid exchange (SCE) than the control level. We detected reactive oxygen species (ROS) in CHO cells treated with the particles. These findings indicate that magnetite nano-particles induce ROS in mammalian cells, leading to the direct or indirect induction of DSB, followed by clastogenic events including MN and SCE.
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In vitro toxicity of nanoparticles in BRL 3A rat liver cells
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