Krętowski Rafał, Kusaczuk Magdalena, Naumowicz Monika, Kotyńska Joanna, Szynaka Beata, Cechowska-Pasko Marzanna
Department of Pharmaceutical Biochemistry, Medical University of Białystok, Mickiewicza 2A, 15-222 Białystok, Poland.
Institute of Chemistry, University of Bialystok, K. Ciołkowskiego 1K, 15-245 Białystok, Poland.
Nanomaterials (Basel). 2017 Aug 21;7(8):230. doi: 10.3390/nano7080230.
Silica nanoparticles (SiNPs) are one of the most commonly used nanomaterials in various medical applications. However, possible mechanisms of the toxicity caused by SiNPs remain unclear. The study presented here provides novel information on molecular and cellular effects of SiNPs in glioblastoma LBC3 and LN-18 cells. It has been demonstrated that SiNPs of 7 nm, 5-15 nm and 10-20 nm induce time- and dose-dependent cytotoxicity in LBC3 and LN-18 cell lines. In contrast to glioblastoma cells, we observed only weak reduction in viability of normal skin fibroblasts treated with SiNPs. Furthermore, in LBC3 cells treated with 5-15 nm SiNPs we noticed induction of apoptosis and necrosis, while in LN-18 cells only necrosis. The 5-15 nm SiNPs were also found to cause oxidative stress, a loss in mitochondrial membrane potential, and changes in the ultrastructure of the mitochondria in LBC3 cells. Quantitative real-time PCR results showed that in LBC3 cells the mRNA levels of pro-apoptotic genes , , , and were significantly upregulated. An increase in activity of caspase-9 in these cells was also observed. Moreover, the activation of SiNP-induced autophagy was demonstrated in LBC3 cells as shown by an increase in LC3-II/LC3-I ratio, the upregulation of gene and an increase in AVOs-positive cells. In conclusion, this research provides novel information concerning molecular mechanisms of apoptosis and autophagy in LBC3 cells.
二氧化硅纳米颗粒(SiNPs)是各种医学应用中最常用的纳米材料之一。然而,SiNPs引起毒性的可能机制仍不清楚。本文介绍的研究提供了关于SiNPs对胶质母细胞瘤LBC3和LN-18细胞分子和细胞效应的新信息。已证明7nm、5-15nm和10-20nm的SiNPs在LBC3和LN-18细胞系中诱导时间和剂量依赖性细胞毒性。与胶质母细胞瘤细胞不同,我们观察到用SiNPs处理的正常皮肤成纤维细胞活力仅轻微降低。此外,在用5-15nm SiNPs处理的LBC3细胞中,我们注意到诱导了凋亡和坏死,而在LN-18细胞中仅观察到坏死。还发现5-15nm SiNPs在LBC3细胞中引起氧化应激、线粒体膜电位丧失以及线粒体超微结构变化。定量实时PCR结果表明,在LBC3细胞中,促凋亡基因、、、和的mRNA水平显著上调。在这些细胞中还观察到caspase-9活性增加。此外,如LC3-II/LC3-I比值增加、基因上调以及自噬空泡(AVOs)阳性细胞增加所示,LBC3细胞中证明了SiNP诱导的自噬激活。总之,本研究提供了关于LBC3细胞凋亡和自噬分子机制的新信息。