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氧化锌量子点诱导HeLa和HEK-293T细胞系的氧化应激和细胞凋亡。

ZnO Quantum Dots Induced Oxidative Stress and Apoptosis in HeLa and HEK-293T Cell Lines.

作者信息

Yang Yanjie, Song Zhenhua, Wu Weixia, Xu Ao, Lv Shuangyu, Ji Shaoping

机构信息

Provincial Engineering Centre for Tumor Molecular Medicine, School of Basic Medical Sciences, Henan University, Kaifeng, China.

出版信息

Front Pharmacol. 2020 Feb 27;11:131. doi: 10.3389/fphar.2020.00131. eCollection 2020.


DOI:10.3389/fphar.2020.00131
PMID:32180717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7057716/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/c417218bf955/fphar-11-00131-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/8cdadfdb41a6/fphar-11-00131-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/0c93237b9352/fphar-11-00131-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/5dd67e06d759/fphar-11-00131-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/56f00db68650/fphar-11-00131-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/488b3e8dc5c6/fphar-11-00131-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/c417218bf955/fphar-11-00131-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/8cdadfdb41a6/fphar-11-00131-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/0c93237b9352/fphar-11-00131-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/5dd67e06d759/fphar-11-00131-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/56f00db68650/fphar-11-00131-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/488b3e8dc5c6/fphar-11-00131-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cad5/7057716/c417218bf955/fphar-11-00131-g006.jpg

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本文引用的文献

[1]
Defect-induced electronic states amplify the cellular toxicity of ZnO nanoparticles.

Nanotoxicology. 2019-9-25

[2]
Role of Autophagy in Zinc Oxide Nanoparticles-Induced Apoptosis of Mouse LEYDIG Cells.

Int J Mol Sci. 2019-8-19

[3]
Zinc Oxide Nanoparticles Induce Autophagy and Apoptosis via Oxidative Injury and Pro-Inflammatory Cytokines in Primary Astrocyte Cultures.

Nanomaterials (Basel). 2019-7-21

[4]
Glioblastoma U-87MG tumour cells suppressed by ZnO folic acid-conjugated nanoparticles: an in vitro study.

Artif Cells Nanomed Biotechnol. 2019-12

[5]
ZnO nanoparticles-associated mitochondrial stress-induced apoptosis and G2/M arrest in HaCaT cells: a mechanistic approach.

Mutagenesis. 2019-9-20

[6]
Zinc Oxide Nanoparticles Exhibit Both Cyclooxygenase- and Lipoxygenase-Mediated Apoptosis in Human Bone Marrow-Derived Mesenchymal Stem Cells.

Toxicol Res. 2019-1

[7]
Effect of the exposure to Mn-doped ZnS nanoparticles on biomarkers in the freshwater western mosquitofish Gambusia affinis.

Int J Environ Health Res. 2018-8-18

[8]
Review of toxicological effect of quantum dots on the liver.

J Appl Toxicol. 2018-8-8

[9]
In vivo biodistribution and toxicology studies of cadmium-free indium-based quantum dot nanoparticles in a rat model.

Nanomedicine. 2018-7-24

[10]
Synthesis and evaluation of the cytotoxic and anti-proliferative properties of ZnO quantum dots against MCF-7 and MDA-MB-231 human breast cancer cells.

Mater Sci Eng C Mater Biol Appl. 2017-12-1

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