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反复暴露于氧化锌纳米颗粒会导致人鼻腔黏膜类器官培养物中的 DNA 损伤。

Repetitive exposure to zinc oxide nanoparticles induces dna damage in human nasal mucosa mini organ cultures.

机构信息

Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, University of Wuerzburg, Germany.

出版信息

Environ Mol Mutagen. 2011 Aug;52(7):582-9. doi: 10.1002/em.20661. Epub 2011 Jul 22.

Abstract

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.

摘要

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。

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