Department of Neuroregeneration, Institute of Experimental Medicine, Czech Academy of Sciences, Vídeňská 1083, 142 20, Prague 4, Czech Republic.
Department of Polymer Particles, Institute of Macromolecular Chemistry, Czech Academy of Sciences, Prague, Czech Republic.
Neurochem Res. 2020 Jan;45(1):159-170. doi: 10.1007/s11064-019-02790-9. Epub 2019 Apr 3.
Superparamagnetic iron oxide nanoparticles (SPIOn) are widely used as a contrast agent for cell labeling. Macrophages are the first line of defense of organisms in contact with nanoparticles after their administration. In this study we investigated the effect of silica-coated nanoparticles (γ-FeO-SiO) with or without modification by an ascorbic acid (γ-FeO-SiO-ASA), which is meant to act as an antioxidative agent on rat peritoneal macrophages. Both types of nanoparticles were phagocytosed by macrophages in large amounts as confirmed by transmission electron microscopy and Prusian blue staining, however they did not substantially affect the viability of exposed cells in monitored intervals. We further explored cytotoxic effects related to oxidative stress, which is frequently documented in cells exposed to nanoparticles. Our analysis of double strand breaks (DSBs) marker γH2AX showed an increased number of DSBs in cells treated with nanoparticles. Nanoparticle exposure further revealed only slight changes in the expression of genes involved in oxidative stress response. Lipid peroxidation, another marker of oxidative stress, was not significantly affirmed after nanoparticle exposure. Our data indicate that the effect of both types of nanoparticles on cell viability, or biomolecules such as DNA or lipids, was similar; however the presence of ascorbic acid, either bound to the nanoparticles or added to the cultivation medium, worsened the negative effect of nanoparticles in various tests performed. The attachment of ascorbic acid on the surface of nanoparticles did not have a protective effect against induced cytotoxicity, as expected.
超顺磁氧化铁纳米颗粒(SPIOn)被广泛用作细胞标记的对比剂。在给予纳米颗粒后,巨噬细胞是与纳米颗粒接触的生物体的第一道防线。在这项研究中,我们研究了涂有二氧化硅的纳米颗粒(γ-FeO-SiO)和/或用抗坏血酸(γ-FeO-SiO-ASA)修饰的纳米颗粒(旨在作为抗氧化剂)对大鼠腹腔巨噬细胞的影响。两种类型的纳米颗粒均被巨噬细胞大量吞噬,这一点通过透射电子显微镜和普鲁士蓝染色得到证实,但它们在监测的时间间隔内并未实质性地影响暴露细胞的活力。我们进一步探讨了与氧化应激相关的细胞毒性作用,这在暴露于纳米颗粒的细胞中经常被记录。我们对双链断裂(DSBs)标志物 γH2AX 的分析表明,用纳米颗粒处理的细胞中 DSBs 的数量增加。纳米颗粒暴露后,仅观察到参与氧化应激反应的基因表达略有变化。脂质过氧化,氧化应激的另一个标志物,在纳米颗粒暴露后没有得到显著证实。我们的数据表明,两种类型的纳米颗粒对细胞活力或生物分子(如 DNA 或脂质)的影响相似;然而,抗坏血酸的存在,无论是结合在纳米颗粒上还是添加到培养介质中,都会在各种测试中加重纳米颗粒的负面效应。如预期的那样,抗坏血酸在纳米颗粒表面的附着并没有对诱导的细胞毒性产生保护作用。