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Ag-NPs 诱导人牙髓干细胞源性神经元细胞凋亡、线粒体损伤和 MT3/OSGIN2 表达变化的体外模型。

Ag-NPs induce apoptosis, mitochondrial damages and MT3/OSGIN2 expression changes in an in vitro model of human dental-pulp-stem-cells-derived neurons.

机构信息

Institute of Neurological Sciences, Italian National Research Council, Catania, Italy.

Institute of Neurological Sciences, Italian National Research Council, Catania, Italy; Department of Biomedical and Biotechnological Sciences, Section of Human Anatomy and Histology, University of Catania, Catania, Italy.

出版信息

Neurotoxicology. 2018 Jul;67:84-93. doi: 10.1016/j.neuro.2018.04.014. Epub 2018 Apr 23.

Abstract

Silver nanoparticles (Ag-NPs) are one of the most popular nanotechnologies because of their unique antibacterial and antifungal properties. Given their increasing use in a wide range of commercial, biomedical and food products, exposure to Ag-NPs is now a reality in people's lives. However, there is a serious lack of information regarding their potential toxic effects in the central nervous system. In this study, we investigated the biocompatibility of "homemade" Ag-NPs in an in vitro model of human neurons derived from dental pulp mesenchymal stem cells. Our results showed that acute exposure to Ag-NPs cause cytotoxicity, by triggering cell apoptosis, damaging neuronal connections, affecting the mitochondrial activity and changing the mRNA expression level of MT3 and OSGIN2, two genes involved in heavy metals metabolism and cellular growth during oxidative stress conditions. Further studies are needed to understand the molecular mechanisms and the physiological consequences underlying Ag-NPs exposure.

摘要

银纳米颗粒(Ag-NPs)因其独特的抗菌和抗真菌特性而成为最受欢迎的纳米技术之一。鉴于它们在广泛的商业、生物医学和食品产品中的应用日益增加,人们的生活中现在已经接触到 Ag-NPs。然而,关于它们在中枢神经系统中的潜在毒性作用的信息却严重缺乏。在这项研究中,我们在源自牙髓间充质干细胞的人神经元体外模型中研究了“自制”Ag-NPs 的生物相容性。我们的结果表明,Ag-NPs 的急性暴露通过触发细胞凋亡、破坏神经元连接、影响线粒体活性以及改变 MT3 和 OSGIN2 的 mRNA 表达水平来引起细胞毒性,这两种基因参与重金属代谢和氧化应激条件下的细胞生长。需要进一步研究来了解 Ag-NPs 暴露的分子机制和生理后果。

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