Department of Psychology, Area of Psychobiology, Edificio de Servicios Centrales de Investigación, Universidade da Coruña, DICOMOSA Group, Campus Elviña s/n, 15071-A Coruña, Spain.
Department of Cell and Molecular Biology, Facultad de Ciencias, Universidade da Coruña, Campus A Zapateira s/n, 15071-A Coruña, Spain.
Environ Mol Mutagen. 2019 Dec;60(9):816-829. doi: 10.1002/em.22323. Epub 2019 Aug 30.
Iron oxide nanoparticles (ION) are gaining importance as diagnostic and therapeutic tool of central nervous system diseases. Although oleic acid-coated ION (O-ION) have been described as stable and biocompatible, their potential neurotoxicity was scarcely evaluated in human nervous cells so far. The primary aim of this work was to assess the molecular and cellular effects of O-ION on human astrocytes (A172 cells) under different experimental conditions. An extensive set of cyto- and genotoxicity tests was carried out, including lactate dehydrogenase release assay, cell cycle alterations, and cell death production, as well as comet assay, γH2AX assay, and micronucleus (MN) test, considering also iron ion release capacity and alterations in DNA repair ability. Results showed a moderate cytotoxicity related to cell cycle arrest and cell death promotion, regardless of serum presence. O-ION induced genotoxic effects, namely primary DNA damage, as detected by the comet assay and H2AX phosphorylation, but A172 cells were able to repair this particular damage because no chromosome alterations were found (confirmed by MN test results). Accordingly, no effects on the DNA repair ability were observed. The presence of serum proteins did not influence O-ION toxicity. Iron ions released from the O-ION surface seemed not to be responsible for the cytotoxic and genotoxic effects observed. Environ. Mol. Mutagen. 2019. © 2019 Wiley Periodicals, Inc.
氧化铁纳米粒子(ION)作为中枢神经系统疾病的诊断和治疗工具越来越受到重视。尽管油酸包覆的 ION(O-ION)已被描述为稳定且具有生物相容性,但迄今为止,其在人类神经细胞中的潜在神经毒性尚未得到充分评估。这项工作的主要目的是评估 O-ION 在不同实验条件下对人星形胶质细胞(A172 细胞)的分子和细胞影响。进行了广泛的细胞毒性和遗传毒性测试,包括乳酸脱氢酶释放测定、细胞周期改变和细胞死亡产生,以及彗星试验、γH2AX 试验和微核(MN)试验,同时还考虑了铁离子释放能力和 DNA 修复能力的改变。结果表明,无论是否存在血清,O-ION 都会引起与细胞周期停滞和促进细胞死亡相关的中等细胞毒性。O-ION 诱导了遗传毒性作用,即通过彗星试验和 H2AX 磷酸化检测到的原发性 DNA 损伤,但 A172 细胞能够修复这种特定的损伤,因为没有发现染色体改变(MN 试验结果证实)。因此,没有观察到对 DNA 修复能力的影响。血清蛋白的存在并不影响 O-ION 的毒性。从 O-ION 表面释放的铁离子似乎不是观察到的细胞毒性和遗传毒性作用的原因。环境分子突变杂志。2019. © 2019 威利父子公司
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