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机构地区:[1]暨南大学医学院发热研究室,广东广州510632 [2]暨南大学医学院血液病研究所,广东广州510632
出 处:《暨南大学学报(自然科学与医学版)》2005年第4期486-490,共5页Journal of Jinan University(Natural Science & Medicine Edition)
基 金:广东省自然科学重点基金(021195);广州市科技计划(2001-Z-037-01)资助项目
摘 要:目的:比较肝癌BEL-7402和SMMC-7721细胞对三氧化二砷(As2O3)诱导凋亡的敏感性差异,探讨细胞内谷胱甘肽(GSH)含量与其作用的关系.方法:不同浓度As2O3作用BEL-7402和SMMC-7721细胞24~96 h,流式细胞仪检测细胞DNA含量,计算细胞凋亡百分率;GSH检测试剂盒检测细胞内GSH含量.结果:0.25 μmol/L As2O3作用24 h,有效地诱导BEL-7402细胞凋亡;对SMMC-7721细胞来说,需要用1.0 μmol/L As2O3作用24 h才能达到相同的抑制效果.1.0 μmol/L As2O3作用72 h时,BEL-7402细胞的凋亡率为(43.8±0.2)%,SMMC-7721细胞的凋亡率为(12.8±0.2)%,检测BEL-7402细胞内GSH为(18.7±1.4) nmol/mg;SMMC-7721细胞内GSH为(50.8±5.2) nmol/mg,两者比较均有显著差异.结论:肝癌BEL-7402和SMMC-7721细胞对As2O3诱导细胞凋亡的敏感性不同,可能与细胞内GSH含量有关.Aim: To compare the susceptive differences of arsenic trioxide (As203) induced apoptosis on BEL- 7402 and SMMC - 7721 cells, and explore the effect of GSH level in cells on them. Methods: The flowcytometry was used to detect the apoptotic percentage and GSH kit to determine the level of GSH while the effect of arsenic trioxide on cells of BEL- 7402 cells and SMMC - 7721 cells reached 24 - 96 hours. Results: Arsenic trioxide is able to induce apoptosis of BEL- 7402 cells at 0.25 μmol/L for 24 hours; however, it needed 1.0μmol/L of As2O3 for 24 hours to produce the similar results for SMMC - 7721 cells. The apoptotic rate of BEL-7402 cells is (43.8 ± 0.2)% at dose of 1.0 μmol/L As2O3 for 72 hours, and the apoptofic rate of SMMC - 7721 is ( 12.8 ± 0.2) % only; at this time, level of GSH in BEL-7402 cells is (18.7 ± 1.4) nmol/mg, and in SMMC- 7721 cells is (50.8 ± 5.2) nmol/mg, which showed the significant difference between them. Conclusion: Tne sensibility difference between BEL - 7402 and SMMC - 7721 hepatocarcinoma cells to As2O3 are related with level of GSH in cells.
关 键 词:BEL-7402细胞 SMMC-7721细胞 三氧化二砷 细胞凋亡 谷胱甘肽
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