Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Wuerzburg, Germany.
Environ Mol Mutagen. 2011 Aug;52(7):582-9. doi: 10.1002/em.20661. Epub 2011 Jul 22.
Data on the toxicological properties of zinc oxide nanoparticles (ZnO-NPs) is incomplete. ZnO-NPs may enter humans via inhalation or ingestion. The aim of the current study was to evaluate ZnO-NP-induced genotoxicity in three-dimensional (3D) mini organ cultures (MOCs) of human nasal mucosa following repeated exposure to ZnO-NP and regeneration. Nasal MOCs of 10 patients and ZnO-NPs were cultivated for one week and then characterized by electron microscopy. Nasal MOCs were partially covered by ciliated epithelium after one week of cultivation. ZnO-NPs were distributed to the cytoplasm and the nucleus. MOCs were exposed once, twice, or three times to 0.1 or 5 μg/ml of ZnO-NPs for 1 hr per exposure and were then evaluated for cytotoxicity and genotoxicity. MOCs were cultivated for 24 hr after the triple ZnO-NP exposure to allow for regeneration. ZnO-NP exposure did not result in significant cytotoxicity or apoptosis, as determined by trypan blue exclusion and caspase-3 activity, respectively. A significant increase in DNA damage was detected following repetitive exposure compared to single exposure to ZnO-NPs at 5 μg/ml, but not 0.1 μg/ml ZnO-NPs. At both concentrations of ZnO-NP, DNA fragmentation increased after 24 hr of regeneration. In contrast, DNA damage which was induced by the positive control, methyl methanesulfonate, was significantly reduced after 24-hr regeneration. Thus, our results suggest that repetitive exposure to low concentrations of ZnO-NPs results in persistent or ongoing DNA damage.
氧化锌纳米粒子(ZnO-NPs)的毒理学性质数据尚不完全。ZnO-NPs 可能通过吸入或摄入进入人体。本研究的目的是评估在反复暴露于 ZnO-NP 并再生后,三维(3D)人鼻黏膜迷你器官培养物(MOC)中 ZnO-NP 诱导的遗传毒性。10 名患者的鼻 MOC 和 ZnO-NPs 培养了一周,然后通过电子显微镜进行了表征。培养一周后,鼻 MOC 部分被纤毛上皮覆盖。ZnO-NPs 分布在细胞质和细胞核中。MOC 单次、两次或三次暴露于 0.1 或 5 μg/ml ZnO-NP 中,每次暴露 1 小时,然后评估细胞毒性和遗传毒性。三重 ZnO-NP 暴露后,MOC 再培养 24 小时以允许再生。通过台盼蓝排除和 caspase-3 活性分别确定,ZnO-NP 暴露不会导致明显的细胞毒性或细胞凋亡。与单次暴露于 ZnO-NP 相比,重复暴露于 ZnO-NP 会导致显著增加的 DNA 损伤,而 0.1 μg/ml ZnO-NP 则不会。在两种浓度的 ZnO-NP 下,再生 24 小时后 DNA 片段化增加。相比之下,阳性对照甲基甲磺酸酯诱导的 DNA 损伤在 24 小时再生后显著减少。因此,我们的结果表明,反复暴露于低浓度的 ZnO-NPs 会导致持续或持续的 DNA 损伤。