硝普钠抑制K562细胞增殖并诱导细胞凋亡的实验研究  

Effects of sodium nitroprusside on proliferation inhibition and apoptosis in K562 cell line

作　　者：周永列[1] 吕亚萍[2] 邱莲女[1] 何国浓[3] 林惠君[1] 王文松[1] 

机构地区：[1]浙江省人民医院中心实验室 [2]浙江工业大学药学院 [3]浙江中医学院生命科学系

出　　处：《中国临床药理学与治疗学》2004年第12期1381-1387,共7页Chinese Journal of Clinical Pharmacology and Therapeutics

基　　金：浙江省医学科学研究基金资助项目 (№ 2 0 0 2A0 0 10

摘　　要：目的 :观察外源性一氧化氮 (NO)供体硝普钠对K5 6 2细胞增殖抑制及诱导细胞凋亡作用。方法 :将不同浓度的硝普钠与K5 6 2细胞在体外培养 ,观察其作用时间效应和剂量效应 ;用活细胞计数、MTT法观察硝普钠对K5 6 2细胞增殖的抑制作用 ;用DNA凝胶电泳、DNA含量及细胞周期分析、Annexin V PI双标记和DNA片段原位末端标记法等分析细胞凋亡。同时设高铁氰化钾 (PFC)对照组和空白对照组。结果 :NO能抑制K5 6 2细胞生长 ,并在一定的剂量范围内呈现作用时间和剂量的量效关系 ,大部分细胞阻滞于G0 G1期 ;K5 6 2细胞与硝普钠作用后出现典型的细胞形态改变 ,DNA片断化 ,亚G1峰检出并显著增加 ,AnnexinV PI和DNA片段原位末端标记表达增加等均证实NO能诱导K5 6 2细胞凋亡。而对照组并无此类变化。结论 :NO通过阻滞G0 G1期细胞显著抑制K5 6 2细胞的增殖 ,并有很强的致凋亡作用。AIM: To study the effects of nitric oxide donor sodium nitro pr usside on proliferation inhibition and apoptosis in K562 human leukemia cell lin e. METHODS: The different concentration of sodium nitroprusside and K562 cell were cultivated at the different time in vitro. The proliferation inhibition was analyzed by MTT assay and alive cell count. Cell apoptosis was an alyzed by cell morphology, DNA agarose gel electrophoresis, DNA content, and Ann exin V/PI labeling method. The TDT-mediated dUTP nick end labeling (TUNEL) ass ay was used to quantitate the cell apoptosis in situ. The PFC and the blank were used as controls. RESULTS: NO inhibited K562 cell proliferation within a certain range of treating time and dosage, and a majority of K562 cell s were arrested in G 0/G 1 phase. The K562 cells apoptosis was confirmed by ty pe cell morphology, DNA fragment, sub-G 1 phase, TUNEL and Annexin V/PI labeli ng method with a time and dosage relationship, and the control group had no chan ge like this. CONCLUTION: NO can suppress proliferation of K562 cell line by arresting G 0/G 1 phase and trigger apoptosis of the line.

关 键 词：硝普钠/一氧化氮 细胞株 K562 增殖 细胞凋亡 

分 类 号：R966[医药卫生—药理学] R972.4[医药卫生—药学]