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Oxidative stress and apoptosis induced by ZnO nanoparticles in HaCaT cells

机译:纳米氧化锌诱导HaCaT细胞氧化应激和凋亡

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Zinc oxide (ZnO) nanoparticles (NPs) are used in the cosmetic industry in cosmetics and sunscreen. ZnO NPs have been reported to elicit various adverse cellular effects, including cytotoxicity. However, the underlying mechanisms of these adverse effects have not been fully characterized. To investigate the potential of cytotoxicity induced by ZnO NPs, we evaluated cytosolic reactive oxygen species levels in human keratinocyte HaCaT cells treated with ZnO NPs having different surface charges and particle sizes. A short period of treatment (30 min) with 100 nm ZnO NPs resulted in a greater increase of cytosolic ROS levels, compared to treatment with 20 nm ZnO NPs at the same concentration. During a long period of treatment (24 h) with ZnO NPs, intracellular ROS was increased in cells treated with 20 mu g/mL 20 nm (+/-) charged ZnO. No significant difference according to differences in surface charge was observed. In addition, total levels of caspase-7 and PARP were decreased by ZnO NPs. These results demonstrated that ZnO NPs could induce ROS mediated apoptosis.
机译:氧化锌(ZnO)纳米颗粒(NPs)用于化妆品工业中的化妆品和防晒霜。据报道,ZnO NPs会引起各种不良细胞效应,包括细胞毒性。但是,这些不良作用的潜在机制尚未完全表征。为了研究由ZnO NPs诱导的细胞毒性的潜力,我们评估了用具有不同表面电荷和粒径的ZnO NPs处理的人角质形成细胞HaCaT细胞中胞浆中活性氧的含量。与使用相同浓度的20 nm ZnO NP进行处理相比,使用100 nm ZnO NP进行的短时间处理(30分钟)导致胞质ROS水平的增加更大。在用ZnO NP进行的长时间处理(24小时)中,用20μg / mL 20 nm(+/-)荷电的ZnO处理的细胞中的细胞内ROS增加。没有观察到根据表面电荷差异的显着差异。此外,ZnO NPs降低了caspase-7和PARP的总水平。这些结果表明ZnO NPs可以诱导ROS介导的细胞凋亡。

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