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中国临床药理学与治疗学 ›› 2007, Vol. 12 ›› Issue (6): 635-638.

• 基础研究 • 上一篇    下一篇

亚砷酸对人骨髓间充质干细胞增殖及凋亡的影响

陈晓晨, 吴德沛, 陈峰, 常伟荣   

  1. 苏州大学附属第一医院, 江苏省血液研究所, 苏州215006, 江苏
  • 收稿日期:2007-02-09 修回日期:2007-04-11 发布日期:2020-11-09
  • 通讯作者: 吴德沛, 男, 主任医师, 教授, 博士生导师, 研究方向:恶性血液病诊治与造血干细胞移植。Tel:0512-67780390 E-mail:wudepei @suda.edu. cn
  • 作者简介:陈晓晨, 男, 硕士研究生, 研究方向:恶性血液病诊治与造血干细胞移植。Tel:0512-67780413 E-mail:chenxiabcd100 @163. com
  • 基金资助:
    卫生部科研课题资助项目(WKJ2004-2-005); 江苏省重点人才基金资助项目(RC2002033)

Effect of arsenic trioxide on proliferation and apoptosis of mesenchymal stem cell of human bone marrow

CHEN Xiao-chen, WU De-pei, CHEN Feng, CHANG Wei-rong   

  1. The First Affiliated Hospital of Suzhou University, Hematology Institute of Jiangsu Province, Suzhou 215006, Jiangsu, China
  • Received:2007-02-09 Revised:2007-04-11 Published:2020-11-09

摘要: 目的:研究亚砷酸(ATO) 对人骨髓间充质干细胞(MSC) 增殖及凋亡的影响。方法:通过正常志愿者髂后上棘穿刺获得MSC, 体外培养传代, 取第3代细胞鉴定后进行实验。纯化的MSC 与1、 5、 10 μmol/L 的ATO 共孵育, 分别在24、 48、 72 h 时采用HE 染色观察细胞形态学变化, MTT 法检测细胞增殖抑制率, 流式细胞术(FCM) 分析细胞凋亡情况。结果:ATO 可引起MSC 形态明显改变;抑制MSC 增殖, 不同浓度(1、 5、 10 μmol/L) ATO 对MSC 作用72 h时的细胞增殖抑制率分别为(66. 3 ±2. 2)% 、(81. 1±1. 7)% 、(90. 0 ±2. 2)% ;FCM 检测表明ATO 可诱导MSC 凋亡, 10 μmol/L 的ATO 处理72 h 时引起(68. 37 ±2. 93)% 的凋亡率。这3 种作用均随ATO浓度及作用时间的增加而增强。结论:ATO 可在体外抑制MSC 增殖, 并促进其凋亡。

关键词: 亚砷酸, 间充质干细胞, 细胞增殖, 细胞凋亡

Abstract: AIM:To study the effect of arsenic trioxide (ATO) on the proliferation and apoptosis of mesenchymal stem cell (MSC) of human bone marrow in vitro.METHODS:MSC from healthy volunteers were cultured in vitro and subcultured for three generations. After being identified, the cells were cultured with different concentrations of ATO (1, 5, 10 μmol/L). After 24, 48 and 72 h, the morphological changes of MSC were observed by HE staining; the inhibition of proliferation was measured by MTT assay, and cell apoptosis was evaluated by flow cytometry.RESULTS:After treatment of ATO, partial cells presented characteristic morphological changes. ATO inhibited the growth of MSC in a concentration-and timedependent manner. Flow cytometry analysis showed that ATO induced apoptosis of MSC, and the percentage of apoptotic cells increased as the concentration increased and time elapsed. While the cells were treated with ATO (10 μmol/L) for 72 h, the percentage of apoptotic cells was 68. 37% ±2. 93% .CONCLUSION: ATO can inhibit proliferation of MSC and promote its apoptosis in vitro.

Key words: arsenic trioxide, mesenchymal stem cell, proliferation, apoptosis

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