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作 者:朱玉胜[1,2,3] 吕元[1,2,3] 林果为[1,2,3] 杨正洪 吕沅冈[1,2,3] 张荣兴 胡晓武[1,2,3]
机构地区:[1]上海医科大学华山医院 [2]中国科学院细胞库 [3]安徽省马鞍山市人民医院检验科
出 处:《上海医科大学学报》1999年第3期191-193,共3页Journal of Fudan University(Medical Science)
摘 要:研究人类白血病细胞株K562及耐长春新碱的K562变异株K562/VCR对长春新碱诱导凋亡的敏感性的差异,以探讨抗凋亡在白血病多药耐药性(MDR)中的作用。方法将K562及K562/VCR分别用浓度为0、0.001、0.010μg/ml的长春新碱诱导24h,用流式细胞仪PI染色法、TUNEL法及ELISA法分别进行细胞凋亡检测。结果经浓度为0、0.001μg/ml长春新碱诱导后,K562细胞凋亡率分别为(4.10±0.17)%、(13.30±3.74)%,而K562/VCR细胞凋亡率分别为(3.61±0.69)%、(9.06±4.24)%,统计学显示两者差异无显著性(n=3,P>0.05)。而长春新碱浓度达0.010μg/ml时,K562及K562/VCR细胞凋亡率分别为(36.48±6.70)%、(10.45±3.71)%,两者差异有极显著意义(n=3,P<0.01)。TUNEL及ELISA检测结果与此类似。结论K562及K562/VCR对长春新碱诱导细胞凋亡的敏感性不同,耐药细胞对药物诱导细胞凋亡的抵抗性增强可能在白血病MDR发生中有重要作用。Purpose To study the sensitivity of human leukemic cell line K562 and vincristine resistant cell variant K562/VCR to vincristin induced apoptosis and explore the effect of antiapoptosis on the multidrug resistance of leukemia. Methods K562 and K562VCR cells were treated with vincristine for 24 hours at the concentration of 0,0.001,0.010 μg/ml respectively.Apoptosis was detected with flow cytometry(FCM),TdT-media ted dUTP nick end labeling(TUNEL),and ELISA. Results After the treatment without vincristine,the apoptotic rate of K562 and K562/VCR was (4.10±0.17)% and (3.61±0.69)% respectively and at the concentration of 0.001 μg/ml,the rate was (13.30±3.74)% and (9.06±4.24)% respectively,as determined by FCM.Statistical analysis showed that there was no significant difference in apoptotic rate between K562 and K562/VCR at the above concentrations( n =3, P >0.05).But as the concentration of vincristine was increased to 0.010 μg/ml,the apoptotic rate of K562(36.48±6.70)% was significantly higher than that of K562/VCR(10.45±3.71)% ( n=3,P< 0.01).Similar results were also obtained with TUNEL and ELISA. Conclusions K562 and K562/VCR cells have defferent sensitivity to vincristine induced apoptosis.The resistance of drug resistant leukemic cells to drug induced apoptosis may play an important role in multidrug resistance of leukemia.
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