Yang Yanjie, Song Zhenhua, Wu Weixia, Xu Ao, Lv Shuangyu, Ji Shaoping
Provincial Engineering Centre for Tumor Molecular Medicine, School of Basic Medical Sciences, Henan University, Kaifeng, China.
Front Pharmacol. 2020 Feb 27;11:131. doi: 10.3389/fphar.2020.00131. eCollection 2020.
Zinc oxide (ZnO) quantum dot (QD) is a promising inexpensive inorganic nanomaterials, of which potential toxic effects on biological systems and human health should be evaluated before biomedical application. In this study, the cytotoxicity of ZnO QDs was assessed using HeLa cervical cancer cell and HEK-293T human embryonic kidney cell lines. Cell viability was significantly decreased by treatment with 50 µg/ml ZnO QDs after only 6 h, and the cytotoxicity of ZnO QDs was higher in HEK-293T than in HeLa cells. ZnO QDs increased the level of reactive oxygen species and decreased the mitochondria membrane potential in a dose-dependent manner. Several gene expression involved in apoptosis was regulated by ZnO QDs, including bcl-2 gene and caspase. In HeLa cells, ZnO QDs significantly increased early and late apoptosis, but only late apoptosis was affected in HEK-293T cells. These findings will be helpful for future research and application of ZnO QDs in biomedicine.
氧化锌(ZnO)量子点(QD)是一种很有前景的廉价无机纳米材料,在生物医学应用之前,应评估其对生物系统和人类健康的潜在毒性作用。在本研究中,使用HeLa宫颈癌细胞系和HEK - 293T人胚肾细胞系评估了ZnO量子点的细胞毒性。仅在6小时后,用50μg/ml ZnO量子点处理就显著降低了细胞活力,并且ZnO量子点对HEK - 293T细胞的细胞毒性高于HeLa细胞。ZnO量子点以剂量依赖的方式增加活性氧水平并降低线粒体膜电位。几种参与凋亡的基因表达受ZnO量子点调控,包括bcl - 2基因和半胱天冬酶。在HeLa细胞中,ZnO量子点显著增加早期和晚期凋亡,但在HEK - 293T细胞中仅晚期凋亡受到影响。这些发现将有助于未来ZnO量子点在生物医学中的研究和应用。
Front Pharmacol. 2020-2-27
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