基础医学与临床 ›› 2013, Vol. 33 ›› Issue (5): 537-541.

• 研究论文 • 上一篇    下一篇

米非司酮对大鼠胚胎神经干细胞存活、增殖及分化的影响

冯敏娟1,2,王媛媛1,焦倩1,杨志倩1,邢兰英3,吕海侠1,刘勇1   

  1. 1. 西安交通大学医学院
    2. 西安交通大学医学院第二附属医院 妇产科
    3. 西安交通大学医学院第二附属医院
  • 收稿日期:2012-07-03 修回日期:2012-09-24 出版日期:2013-05-05 发布日期:2013-05-29
  • 通讯作者: 吕海侠 E-mail:hxl01@mail.xjtu.edu.cn
  • 基金资助:
    缺血缺氧脑损伤后神经营养素3诱导神经再生的miRNA机制研究;利用低氧诱导因子调控基因修饰BDNF表达的脑缺血损伤保护和干细胞增殖分化作用研究

Effect of mifepristone on the survival, proliferation and differentiation of rat embryonic neural stem cell in vitro

  • Received:2012-07-03 Revised:2012-09-24 Online:2013-05-05 Published:2013-05-29

摘要: 目的 观察米非司酮处理后大鼠胚胎神经干细胞(NSCs)增殖、凋亡和分化变化,分析其对神经发育的可能影响。方法 以不同浓度米非司酮处理体外培养的NSCs,通过活细胞计数、流式细胞仪检测细胞周期及线粒体膜电位、免疫细胞化学染色等方法检测NSCs存活、增殖、凋亡及分化情况。结果 10-5 mol/L米非司酮处理后NSCs存活和增殖明显下降(P<0.05),10-6 和10-8 mol/L对细胞无明显影响,而10-7 mol/L处理第4天后细胞增殖明显,但其对NSCs线粒体膜电位及增殖指数影响不大;处理后NSCs仍保持多向分化能力,神经元和胶质细胞分化比例与对照组相比无差异。结论 大剂量米非司酮抑制NSCs增殖,小剂量则促进细胞增殖、不影响NSCs命运决定。

关键词: 米非司酮, 神经干细胞, 增殖/分化, 凋亡

Abstract: Objective To observe the effect of mifepristone on the survival, proliferation and differentiation of rat embryonic neural stem cells (NSCs) in vitro and then to investigate its effect on neural development. Methods Different concentrations of mifepristone were used to treat the cultured rat embryonic NSCs. Cell counting kit-8 (CCK-8), growth curve, flow cytometry and immunocytochemistry staining were used to investigate the viability, proliferation, apoptosis and differentiation of NSCs. Results NSCs viability and proliferation significantly reduced after treatment of 10-5 mol/L mifepristone (P<0.05). No significant difference was observed after the treatment with mifepristone at 10-6 and 10-8 mol/L. Mifepristone at 10-7 mol/L enhances the proliferation of NSCs, but did not affect its mitochondrial membrane potential and the multiple differentiation. There is no significant difference in the ratio of differentiated β-tubulin Ⅲ+ neurons and GFAP+ glia. Conclusion Effect of mifepristone on NSCs is dosage dependent. Mifepristone at high concentration (10-5 mol/L) attenuates the survival and proliferation of NSCs. However, 10-7 mol/L mifepristone does not affect NSCs apoptosis and differentiation but enhances their proliferation.

Key words: mifepristone, neural stem cells, proliferation/differentiation, apoptosis

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