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中国临床药理学与治疗学 ›› 2010, Vol. 15 ›› Issue (8): 847-850.

• 基础研究 • 上一篇    下一篇

锰超氧化物歧化酶模拟化合物通过Fas途径诱导白血病K562细胞凋亡

范临兰1, 李娟1, 魏虎来1, 窦伟2, 刘伟生2   

  1. 1兰州大学医学实验中心,甘肃省新药临床前研究重点实验室; 2兰州大学化学化工学院, 兰州 730000,甘肃
  • 收稿日期:2010-03-11 修回日期:2010-04-24 出版日期:2010-08-26 发布日期:2020-09-17
  • 通讯作者: 魏虎来,男,教授,博士生导师,研究方向:细胞分子生物学、遗传学。Tel: 0931-89155082 E-mail: weihulai@lzu.edu.cn
  • 作者简介:范临兰,女,硕士,助理研究员,研究方向:细胞分子生物学、肿瘤药理学。Tel:0931-8915391 E-mail: fanll@lzu.edu.cn
  • 基金资助:
    甘肃省新药临床前研究重点实验室开放基金项目(GSKFKT-0702)

MnSODm induces apoptosis in leukemia K562 cells through Fas-dependent pathway

FAN Lin-lan1, LI Juan1, WEI Hu-lai1, DOU Wei2, LIU Wei-sheng2   

  1. 1Laboratory Center for Medical Science, Lanzhou University,Key Laboratory of Preclinical Study for New Drugs of Gansu Province; 2College of Chemistry & Chemic Engineering, Lanzhou University, Lanzhou 730000, Gansu,China
  • Received:2010-03-11 Revised:2010-04-24 Online:2010-08-26 Published:2020-09-17

摘要: 目的: 探讨锰超氧化物歧化酶模拟化合物(mimics of manganese superoxide dismutase, MnSODm) 对人白血病 K562细胞的凋亡诱导效应及作用机制。方法: 应用MTT比色法、Annexin V/ PI 双标记和细胞形态学法观察细胞凋亡;流式细胞术(FCM)测定Fas蛋白表达水平;RT-PCR检测Caspase-3 mRNA的表达水平,比色法测定Caspase-3 活性变化。结果: MnSODm作用后K562细胞的增殖受到抑制,Annexin V/ PI染色显示凋亡细胞明显增多,透射电镜观察呈现典型的凋亡形态改变。同时,Fas蛋白表达水平显著增高,Caspase-3 mRNA表达水平明显升高,活性显著增强。结论: MnSODm可能通过Fas途径诱导白血病K562细胞凋亡。

关键词: 锰超氧化物歧化酶模拟化合物, 白血病, 细胞凋亡, Fas蛋白, Caspase-3

Abstract: AIM: To investigate the apoptosis of human leukemia cell line K562 induced by mimics of manganese superoxide dismutase (MnSODm) in vitro and the possible molecular mechanisms.METHODS: The apoptosis in K562 cells was examined by MTT colorimetric method, FITC-Annexin V and propidium iodide (PI) double staining and morphological changes method, the expression level of Fas protein was measured with flow cytometry(FCM), and the mRNA expression and the activity of Caspase-3 were detected by RT-PCR and colorimetric assay,respectively.RESULTS: After administration with MnSODm, the proliferation of K562 cells was obviously inhibited, the cellular apoptosis was markedly enhanced with Annexin V/PI staining and the cells showed the typical apoptotic morphological changes. The expression of Fas protein in K562 cells up-regulated greatly, which accompanied with the significant increase of both mRNA expression and activity of Caspase-3.CONCLUSION: The apoptosis of leukemia K562 cells induced by MnSODm may involved in the Fas death receptor pathway.

Key words: Mimcs of MnSOD, Leukemia, Apoptosis, Fas protein, Caspase-3

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