1. 暨南大学光电信息与传感技术广东普通高校重点实验室
2. 暨南大学化学系
3. 暨南大学医学院
4. 暨南大学第一临床医学院
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陈伟, 王穗湘, 胡小毛, 等. AFM研究蝙蝠葛碱对daudi细胞毒性的影响[J]. 分析测试学报, 2012,31(3):247-245.
Study of Cell Toxicity of Dauricine on Daudi Cells Based on Atomic Force Microscope[J]. 2012,31(3):247-245.
利用原子力显微镜、CCK-8实验和流式细胞术研究了蝙蝠葛碱(dauricine)对B细胞淋巴瘤daudi细胞的细胞毒性。蝙蝠葛碱能显著抑制daudi细胞的增殖。CCK-8实验表明,细胞存活率与蝙蝠葛碱浓度存在时间依赖和剂量依赖关系。经10~50 μmol/L的蝙蝠葛碱作用24 h后,daudi细胞存活率从(89.8±4.3)%降至(11.2±3.2)%;48 h后,存活率从(68.9±2.6)%降至(2.5±0.5)%。流式细胞术表明蝙蝠葛碱处理daudi细胞24 h后,凋亡率从5.2%增至28.2%(60 μmol/L)。AFM数据显示对照组细胞呈圆形,表面较光滑。经蝙蝠葛碱处理后,daudi细胞坍塌,超微结构显示细胞表面粗糙、凹凸不平。此外,经不同浓度蝙蝠葛碱作用的daudi细胞,其线粒体膜电位随着药物浓度的加大而降低。蝙蝠葛碱能显著抑制daudi细胞生长增殖。
The toxicity of dauricine on daudi cell of B cell lymphoma was investigated by atomic force microscopy,CCK-8 assay and flow cytometer method.The results showed that dauricine could suppress the proliferation of daudi cells.By CCK-8 assay,it was found that cell viability was related with the reaction time and drug concentration.When 10-50 μmol/L dauricine was incubated with daudi cells for 24 h and 48 h,respectively,the cell viability declined from (89.8±4.3)% to (11.2±3.2)% and (68.9±2.6)% to (2.5±0.5)%,respectively.In addition,daudi cells were cultured with different concentrations of dauricine for 24 h,the result revealed that the apoptosis rate increased from 5.2% to 28.2% (60 μmol/L).AFM data showed that control cells were round and the surface was smooth.After treated with dauricine,daudi cell collapsed, the ultrastructure revealed that cell surface was rough and full of bumps and holes.Furthermore,daudi cells were treated with different concentrations of dauricine,the mitochondrial membrane potential of cell decreased with the increase of the dauricine concentration.Dauricine significantly inhibited the growth and proliferation of daudi cells.
蝙蝠葛碱原子力显微镜细胞毒性超微结构daudi细胞细胞凋亡
dauricineatomic force microscopecell toxicityultrasructuredaudi cellcell apoptosis
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