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作 者:欧阳艳艳[1] 姜涛[1] 高萌[1] 肖利华[2] 周杨[1] 顿月丽 赵桂秋[1] 刘世海[3] 梁晔[3]
机构地区:[1]青岛大学医学院附属医院眼科,中国山东省青岛市266003 [2]北京武警总医院眼眶病研究所,中国北京市100039 [3]青岛大学医学院附属医院中心实验室,中国山东省青岛市266003
出 处:《国际眼科杂志》2014年第2期232-235,共4页International Eye Science
基 金:山东省自然科学基金资助项目(No.ZR2012HM062)~~
摘 要:目的:探讨线粒体膜电位(△ψm)、Caspase 3在As2O3诱导ACC-2细胞凋亡中的作用。方法:进行ACC-2细胞培养,将As2O3建立不同药物浓度梯度(0,1.0,2.0,4.0,8.0μmol/L)分别作用于ACC-2细胞,用Rh123染色,流式细胞仪检测8.0μmol/L As2O3作用前、后(24h),ACC-2细胞的线粒体膜电位(△ψm)变化;用多功能酶标仪进行Caspase 3活性检测。结果:空白对照组ACC-2细胞内Rh123荧光强度最强,8.0μmol/L As2O3处理组ACC-2细胞内Rh123荧光强度减弱,其差异有显著性(P<0.05);随着As2O3药物浓度的增高(0,1,2,4,8μmol/L),ACC-2细胞的Caspase 3酶活力单位逐渐增加。结论:As2O3作用于ACC-2细胞,可通过降低线粒体膜电位从而引起细胞凋亡。随着As2O3药物浓度的增高,ACC-2细胞的Caspase 3酶活力单位逐渐增加,Caspase 3被激活,细胞可发生不可逆转的凋亡过程。AIM: To investigate the membrane potential (△ψm) and cell apoptosis induced by As203. role of mitochondrial Caspase 3 in the ACC-2 METHODS: ACC-2 cells were cultured. The As2 03 of different drug concentration gradients (0, 1.0, 2.0, 4.0, 8.0wmol/L) were applied to ACC-2 cells respectively. The changes in △ψm of ACC-2 cells before and after As2 O3's inducing (8.0w mol/L for 24h) were detected by flow cytometry with Rh123 staining. Caspase 3 activity was detected by the multifunctional microplate reader. RESULTS: Rh123 fluorescence intensity in ACC-2 cells was strongest in the control group, while it weakened in ACC-2 cells in 8.0wmol/L As203 treatment group. The difference between two groups was significant (P〈0.05). With the increase of As2 03 concentration (0, 1. 0, 2.0, 4. 0, 8.0p mol/L), Caspase 3 enzyme activity unit in ACC-2 cells gradually increased. CONCLUSION : As2 03 can induce apoptosis of ACC- 2 cells by reducing △ψm. Caspase 3 enzyme activity unit of ACC-2 cells gradually increases with As2 03 concentration increases, which results in activation of the expression of Caspase 3, and the cells' irreversible apoptosis process coming immediately.
关 键 词:三氧化二砷 腺样囊性癌ACC-2细胞 凋亡 线粒体膜电位 半胱氨酸蛋白酶3
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