首页 | 本学科首页   官方微博 | 高级检索  
     

纳米二氧化铈对神经细胞PC12及SH-SY5Y活力的影响
引用本文:许逸岚,赵镘娜,朱诗涵,韩瑜颖,章佳瑜,沈铄恒,俞樟森,张衡. 纳米二氧化铈对神经细胞PC12及SH-SY5Y活力的影响[J]. 中国应用生理学杂志, 2020, 36(1): 62-66. DOI: 10.12047/j.cjap.5810.2020.014
作者姓名:许逸岚  赵镘娜  朱诗涵  韩瑜颖  章佳瑜  沈铄恒  俞樟森  张衡
作者单位:绍兴文理学院医学院基础医学部, 浙江 绍兴 312000
基金项目:国家自然科学基金项目(31800891);浙江省新苗人才计划项目(2018R432029,2019R432025)。
摘    要:目的:探究纳米二氧化铈(CeO2)对神经细胞PC12与SH-SY5Y活力的影响。方法:合成纳米CeO2材料,并对其结构进行表征,性能进行评估。用不同终浓度(1、2.5、5、10、25、50、75、100、150 μg/ml)的纳米CeO2分别处理PC12细胞与SH-SY5Y细胞24 h,使用MTT法检测其细胞活力。然后使用活性氧清除剂NAC与纳米CeO2共孵育处理PC12细胞与SH-SY5Y细胞,并用DCFH-DA探针染色,在荧光倒置显微镜下观察各组细胞的数量及其荧光强度。对实验数据采用单因素方差(one-way ANOVA)分析。结果:纳米CeO2处理后,PC12细胞(P<0.01)与SH-SY5Y细胞(P<0.01)的活力都明显下降,与对照组差异明显。DCFH-DA探针染色后,发现纳米CeO2的浓度越高,荧光强度越强,表明有活性氧(ROS)的产生。活性氧清除剂NAC与纳米CeO2(100 μg/ml)共同处理PC12后,荧光强度明显减弱。与25 μg/ml (P<0.01)、50 μg/ml(P<0.01)、75 μg/ml(P<0.01)、100 μg/ml(P<0.01)纳米CeO2处理组相比,共同处理组细胞活力明显增加。结论:纳米CeO2对神经细胞PC12与SH-SY5Y的活力有明显的抑制作用,其机制可能与ROS有关。

关 键 词:纳米CeO2  活性氧  神经细胞  细胞活力  阿尔茨海默病  

Effects of CeO 2 nanoparticles on the viabilities of neural PC12 and SH-SY5Y cells
XU Yi-lan,ZHAO Man-na,ZHU Shi-han,HAN Yu-ying,ZHANG Jia-yu,SHEN Shuo-heng,YU Zhang-sen,ZHANG Heng. Effects of CeO 2 nanoparticles on the viabilities of neural PC12 and SH-SY5Y cells[J]. Chinese journal of applied physiology, 2020, 36(1): 62-66. DOI: 10.12047/j.cjap.5810.2020.014
Authors:XU Yi-lan  ZHAO Man-na  ZHU Shi-han  HAN Yu-ying  ZHANG Jia-yu  SHEN Shuo-heng  YU Zhang-sen  ZHANG Heng
Affiliation:School of Medicine, Shaoxing University, Shaoxing 312000, China
Abstract:Objective:To investigate the effects of cerium oxide(CeO 2)nanoparticles on the viabilities of nerve cells PC12 and SH-SY5Y.Methods:CeO 2 nanoparticles were synthesized,structures were characterized and properties were evaluated.PC12 cells and SH-SY5Y cells were treated with CeO 2 nanoparticles at different concentrations(1,2.5,5,10,25,50,75,100,150μg/ml)for 24 h and the cell viability was measured by MTT assay.Then PC12 cells and SH-SY5Y cells were co-treated with CeO 2 and active oxygen scavenger NAC and the cells were stained with DCFH-DA probe for ROS.The number of cells and the fluorescence intensity were observed under a fluorescent inverted microscope.Differences were assessed by one-way ANOVA.Results:After treatment with CeO 2 nanoparticles,the viabilities of both PC12 cells(P<0.01)and SH-SY5Y cells(P<0.01)were decreased comparing with the control group.After staining with DCFH-DA probe,the fluorescence intensity of the nerve cells was enhanced depending on the concentration of CeO 2 nanoparticles suggesting that CeO 2 induced the generation of reactive oxygen species(ROS).The fluorescence intensity of PC12 cells was decreased after CeO 2 nanoparticles(100μg/ml)co-treatment with active oxygen scavenger NAC.Compared with CeO 2 nanoparticles alone at 25μg/ml(P<0.01),50μg/ml(P<0.01),75μg/ml(P<0.01),100μg/ml(P<0.01),the cell viability was significantly increased after co-treatment with NAC.Conclusion:CeO 2 nanoparticles has a negative effect on the viabilities of nerve cells PC12 and SH-SY5Y,and the effect might be depend on ROS.
Keywords:CeO 2 nanoparticles  reactive oxygen species  neural cells  cell viability  Alzheimer’s disease
本文献已被 CNKI 维普 等数据库收录!
点击此处可从《中国应用生理学杂志》浏览原始摘要信息
点击此处可从《中国应用生理学杂志》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号