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黄芪皂甙诱导小鼠神经干细胞向神经元分化
引用本文:刘静,罗雪,钟善传,刘宏亮,姚忠祥.黄芪皂甙诱导小鼠神经干细胞向神经元分化[J].第四军医大学学报,2009,30(7):580-583.
作者姓名:刘静  罗雪  钟善传  刘宏亮  姚忠祥
作者单位:刘静,LIU Jing(第三军医大学西南医院康复理疗科,重庆,400038;第四军医大学西京医院康复理疗科,陕西,西安,710033);罗雪,钟善传,姚忠祥,LUO Xue,ZHONG Shan-Chuan,YAO Zhong-Xiang(第三军医大学组织胚胎学教研室,重庆,400038);刘宏亮,LIU Hong-Liang(第三军医大学西南医院康复理疗科,重庆,400038)  
摘    要:目的:观察黄芪皂甙对体外培养的小鼠神经干细胞(NSCs)向神经元分化的影响.方法:采用机械分离、无血清传代培养法从胚胎(E14.5)小鼠室管膜前下区获得NSCs,观察不同浓度(20,40,60mg/L)黄芪皂甙在干预后不同时段(3,7d)的分化情况,通过免疫荧光检测神经元(β-Tubulin),星形胶质细胞(GFAP)及少突胶质细胞(CC-1)的比例,并采用银杏内酯B(40mg/L)作为阳性对照,正常组为阴性对照,观察黄芪皂甙对小鼠NSCs分化的影响.结果:加入黄芪皂甙培养3,7d后,黄芪皂甙40mg/L及60mg/L组、银杏内酯B组分化为β-Tubulin(+)神经元比例均显著高于正常对照组,黄芪皂甙两种浓度组间无统计学差异;银杏内酯B组分化为GFAP(+)星形胶质细胞比例显著高于正常对照组,而黄芪皂甙对星形胶质细胞的分化比例无明显影响.结论:黄芪皂甙能促进NSCs定向分化为神经元,而银杏内酯B促进NSCs向神经元和星形胶质细胞分化.

关 键 词:黄芪皂甙  银杏内酯B  神经干细胞  分化

Effects of Saponins of Astragalus on differentiation of neural stem cells
LIU Jing,LUO Xue,ZHONG Shan-Chuan,LIU Hong-Liang,YAO Zhong-Xiang.Effects of Saponins of Astragalus on differentiation of neural stem cells[J].Journal of the Fourth Military Medical University,2009,30(7):580-583.
Authors:LIU Jing  LUO Xue  ZHONG Shan-Chuan  LIU Hong-Liang  YAO Zhong-Xiang
Institution:LIU Jing1,2,LUO Xue3,ZHONG Shan-Chuan3,LIU Hong-Liang1,YAO Zhong-Xiang31Department of Physical Medicine and Rehabilitation,Southwest Hospital,3Department of Histology and Embryology,Third Military Medical University,Chongqing 400038,China,2Department of Physical Medicine and Rehabilitation,Xijing Hospital,Fourth Military Medical University,Xi'an 710033
Abstract:AIM: To observe the effects of Saponins of Astragalus(SA) of various concentrations on the differentiation of neural stem cells(NSCs). METHODS: NSCs from the anterior subventricular zone of the embryonic mouse ( EI4.5 ) were generated by mechanical isolation and serum-free culture. To study the effects of different concentrations (20, 40, 60 mg/L ) of SA on the differentiation of the NSCs at different stages ( 3 and 7 d) , we adopted immunofluorescence to examine the proportion of the neuron( 3-Tubulin), astrocyte(GFAP) and oligodendrocyte (CC-I) by adding different concentrationsof SA. 40 mg/L Ginkgolide B (GKB) was employed as positive control of SA and normal medium was employed as negative control. RESULTS: The proportion of β-Tubulin positive neurons significantly increasedafter 3 and 7 d cuhure with SA of 40 and 60 mg/L and the GKB and no significant difference was observed between 40 and 60 mg/L of SA. The proportion of GFAP positive astrocytes increased significantly with the adding of GKB, while SA had no obvious effects on the differentiation of the astrocytes. CONCLUSION: Saponins of Astragalus specifically promotes NSCs to differentiate into neurons, while GKB promotes the NSCs to differentiate into both neurons and astrocytes.
Keywords:saponins of astragalus  ginkgolide B  neural stem cells  differentiation  
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