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丙戊酸钠抑制HL-60细胞增殖并诱导其凋亡与分化
引用本文:韩冬梅,陈协群,梁蓉,董宝侠,尹文. 丙戊酸钠抑制HL-60细胞增殖并诱导其凋亡与分化[J]. 中国实验血液学杂志, 2006, 14(1): 21-24
作者姓名:韩冬梅  陈协群  梁蓉  董宝侠  尹文
作者单位:1. 第四军医大学西京医院血液内科,西安,710032
2. 第四军医大学微生物教研室,西安,710032
摘    要:为进一步研究丙戊酸钠(sodium valproate;VPA)对白血病细胞HL-60的增殖、凋亡和分化的影响,采用MTT法检测不同浓度的VPA对HL-60细胞增殖的作用;细胞化学染色法观察药物作用后细胞形态的变化;NBT还原实验结合形态学作为观测细胞分化指标;应用流式细胞术检测不同浓度药物作用后细胞周期的变化及凋亡细胞的比例。结果显示:VPA能明显抑制HL-60的增殖;经2mmol/L VPA处理24-48小时后,HL-60出现胞浆空泡、核固缩、核碎裂及凋亡小体;Annexin V阳性的早期凋亡细胞比例由2.9%升高到17.1%;流式细胞术检测出明显的亚二倍体峰;G1期细胞由51.1%增加至84.6%,S期细胞由37.9%减低至14.4%。0.25mmol/L VPA作用1周后,促进HL-60细胞向中幼粒、晚幼粒阶段分化,NBT阳性细胞百分率为(47±2)%。结论:VPA能明显抑制白血病细胞HL-60的增殖,并诱导其分化及凋亡。

关 键 词:丙戊酸钠  HL-60细胞  细胞增殖  细胞凋亡  细胞分化
文章编号:1009-2137(2006)01-0021-04
收稿时间:2005-03-07
修稿时间:2005-12-02

Inhibition of Proliferation and Induction of Apoptosis and Differentiation of Leukemic Cell Line HL-60 by Sodium Valproate
HAN Dong-Mei,CHEN Xie-Qun,LIANG Rong,DONG Bao-Xia,YIN Wen. Inhibition of Proliferation and Induction of Apoptosis and Differentiation of Leukemic Cell Line HL-60 by Sodium Valproate[J]. Journal of experimental hematology, 2006, 14(1): 21-24
Authors:HAN Dong-Mei  CHEN Xie-Qun  LIANG Rong  DONG Bao-Xia  YIN Wen
Affiliation:Department of Hematology, Xijing Hospital, The Fourth Military Medical University, Xi'an 710032, China.
Abstract:To investigate the influence of sodium valproate (VPA) on proliferation, apoptosis and differentiation of HL-60 cell line, effect of VPA in various concentrations on proliferation of HL-60 cells was detected by MMT; Wright-Giemsa staining was performed to observe the morphologic changes of HL-60 cells; NBT experiment was used to test the differentiation of HL-60 cells; flow cytometry was used to observe cell cycles and analyze the apoptosis. The results indicated that the changes of the growth curve showed inhibition of proliferation of HL-60 cells. After a 24-48 hours culture with 2 mmol/L VPA, the cells exhibited nuclear shrinkage, pyknosis fragmentation and appearance of apoptosis bodies. The percentage of the annexin V(+)/PI(-) cells which were apoptotic increased from 2.9% to 17.1%; hypodiploid peak was observed; the percentage of HL-60 cells in G(1) phase increased from 51.1% to 84.6% and the cells in S phase decreased from 37.9% to 14.4%. After a week culture with 0.25 mmol/L VPA, the cells exhibited characteristics of differentiation. The percentage of NBT positive cells was (47 +/- 2)%. It is concluded that VPA can inhibit the proliferation of HL-60 cells while inducing differentiation and apoptosis of these cells. The mechanism needs to be further studied.
Keywords:sodium valproate   HL-60 cell   cell proliferation   cell apoptosis   cell differentiation
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