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左旋门冬酰胺酶与盐霉素联合作用对急性T淋巴细胞白血病Jurkat细胞株增殖凋亡的影响
引用本文:朱锦灿,陈小宇,刘成成,祝爱珍,刘革修,曾慧兰.左旋门冬酰胺酶与盐霉素联合作用对急性T淋巴细胞白血病Jurkat细胞株增殖凋亡的影响[J].中国病理生理杂志,2013,29(12):2272-2276.
作者姓名:朱锦灿  陈小宇  刘成成  祝爱珍  刘革修  曾慧兰
作者单位:暨南大学 1附属第一医院血液科, 2医学院血液病研究所, 广东 广州 510632
基金项目:国家自然科学基金资助项目(No. 81270568)
摘    要: 目的:研究左旋门冬酰胺酶(L-asparaginase,L-ASP)与盐霉素(salinomycin,Sal)联合作用对急性T淋巴细胞白血病Jurkat细胞株增殖和凋亡的影响及其机制。方法:CCK-8试剂盒检测细胞增殖情况;Western blotting方法检测凋亡相关蛋白Bcl-2、caspase-3、caspase-8、caspase-9及细胞色素C表达的变化;流式细胞术分析各实验组细胞凋亡率之间的差别。结果:不同浓度的L-ASP和Sal单独处理Jurkat细胞株后均显示出明显的增殖抑制作用,L-ASP的IC50为812 IU/L,Sal 的IC50为0.75 μmol/L。而两药联合使用的增殖抑制作用更显著(P<0.05);合用指数计算公式结果显示两药为协同作用。Western blotting 显示联合用药组与L-Asp、Sal单独处理组相比,Bcl-2蛋白表达明显减少,caspase-3、caspase-8、caspase-9和胞浆细胞色素C水平明显增高;干预48 h后行流式细胞术检测结果显示L-ASP(25 IU/L)单独处理组和Sal(0.5μmol/L)单独处理组细胞凋亡率分别为(7.11±0.23)%和(25.43±047)%,与对照组(6.67±0.13)%比较差别有统计学意义(P<0.05),联合用药组细胞凋亡率(39.12±1.97)%分别与L-ASP、Sal单独处理组比较,差别有统计学意义(P<0.05)。结论:左旋门冬氨酸酶与盐霉素联合作用于Jurkat细胞具有协同抑制增殖和诱导凋亡的作用。

关 键 词:门冬酰胺酶  盐霉素  急性T细胞白血病  细胞增殖  细胞凋亡  
收稿时间:2013-07-05

Effects of salinomycin combined with L-asparaginase on proliferation and apoptosis of human acute T-cell leukemia Jurkat cells
ZHU Jin-can,CHEN Xiao-yu,LIU Cheng-cheng,ZHU Ai-zhen,LIU Ge-xiu.Effects of salinomycin combined with L-asparaginase on proliferation and apoptosis of human acute T-cell leukemia Jurkat cells[J].Chinese Journal of Pathophysiology,2013,29(12):2272-2276.
Authors:ZHU Jin-can  CHEN Xiao-yu  LIU Cheng-cheng  ZHU Ai-zhen  LIU Ge-xiu
Institution:Institute of Hematology, School of Medicine, Jinan University, Guangzhou 510632, China.
Abstract:AIM:To investigate the effects of salinomycin alone or in combination with L-asparaginase on the growth and apoptosis of human acute T-cell leukemia Jurkat cells, and the possible mechanism. METHODS:The growth of Jurkat cells was tested by Cell Counting Kit-8 in vitro. The levels of cytochrome C, Bcl-2, caspase-3, caspase-8 and caspase-9 were measured by Western blotting. Flow cytometry was used to assay cell apoptosis. RESULTS:Salinomycin or L-asparaginase alone inhibited the growth of Jurkat cells in a dose-dependent manner. The IC50 value of L-asparaginase was 8.12 IU/L, while that of salinomycin was 0.75 μmol/L. Salinomycin combined with L-asparaginase induced more significant inhibition of cell proliferation (P<0.05). Western blotting showed that the expression of Bcl-2 protein in combination group was significantly reduced, and the expression of caspase-3, caspase-8, caspase-9 and cytochrome C was significantly increased (P<0.05). Flow cytometry showed that the apoptotic rates of Jurkat cells incubated with salinomycin (0.5 μmol/L), L-asparaginase (2.5 IU/L) and both drugs for 48 h were (7.11±0.23)%, (25.43±0.47)% and (39.12±1.97)%, respectively, and significantly higher than that in control group [(6.67±0.13)%, P<0.05].CONCLUSION: Salinomycin synergizes with L-asparaginase-induced cytotoxicity in vitro, and the combined treatment with salinomycin and L-asparaginase induces the apoptosis of Jurkat cells.
Keywords:Asparaginase  Salinomycin  Acute T-cell leukemia  Cell proliferation  Apoptosis
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