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作 者:鲍一笑[1] 余润泉[1] 张登海[1] 李莉[1] 张玲珍[1] 徐玲玲[1] 孔宪涛[1]
机构地区:[1]第二军医大学附属长征医院
出 处:《中华血液学杂志》1999年第3期146-148,共3页Chinese Journal of Hematology
摘 要:目的探讨雷公藤红素对人肥大细胞白血病的作用及机制。方法以人肥大细胞白血病细胞系HMC1细胞为靶细胞,观察雷公藤红素对HMC1细胞凋亡的诱导作用。结果①0.12~1.00μmol/L雷公藤红素可以引起HMC1细胞凋亡,表现为细胞呈凋亡形态学改变,DNA琼脂糖凝胶电泳出现梯形条带,流式细胞仪分析HMC1细胞在G1期前出现凋亡峰;②凋亡率随药物浓度的增加及作用时间的延长而递增;③促进G1期细胞进入S期,使S期细胞比例升高,随后凋亡率升高,S期细胞下降,两者呈负相关(P<0.01);④雷公藤红素可使HMC1细胞bax、cmyc表达增加,bcl2表达下降。结论雷公藤红素可有效地诱导HMC1细胞凋亡,凋亡主要发生在S期,凋亡的发生与其上调促进凋亡基因bax、cmyc和下调抑凋亡基因bcl2的表达有关。Objective To explore the effect of tripterine on leukemic mast cells. Methods The human leukemic mast cell line (HMC 1) was used as target cells for the tripterine’s effect. Results ①Apoptosis of HMC 1 cells could be efficiently induced by tripterine (0.125~1.0μmol/L), showing the apoptotic changes in morphology, DNA ladder on argarose gel electrophoresis and apoptotic peak before G 1 phase of cell cycle on flowcytometry. ② The magnitude of apotosis increased with the augmentation of tripterine concentration and duration of exposure; ③ With G 1 phase cells decreasing, S phase cells were increased, and then apoptotic cells increased with a diminution of S phase cells. They bored significant negative relation (P<0 01);④Tripterine could upregulate bax, c myc expression and downregulate bcl 2 expression at protein level. Conclusion Tripterine can efficiently induce HMC 1 cell apoptosis, occurring mainly in S phase, which is correlated with upregulating bax, c myc expression and downregulating bcl 2 expression.
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