›› 2011, Vol. 42 ›› Issue (6): 726-730.doi: 10.3969/j.issn.0529-1356.2011.06.002

• 神经生物学 • 上一篇    下一篇

脑源性神经营养因子过表达促进大鼠神经干细胞向神经元分化

欧阳长杰; 滕大才; 曲德伟; 王德广; 徐铁军*   

  1. 徐州医学院人体解剖学教研室,江苏 徐州 221002
  • 收稿日期:2011-05-26 修回日期:2011-06-30 出版日期:2011-12-06
  • 通讯作者: 徐铁军*

erived neurotrophic factor overexpression promoting the differentiation of rat neural stem cells into neurons

  1. Department of Human Anatomy,Xuzhou Medical College,Jiangsu Xuzhou 221002, China
  • Received:2011-05-26 Revised:2011-06-30 Online:2011-12-06

关键词: 脑源性神经营养因子, 基因表达, 神经干细胞, 分化, 反转录-聚合酶链式反应, 免疫组织化学, 大鼠

Abstract: Objective To construct eukaryotic expression vector of brain-derived neurotrophic factor (BDNF) and detect its effect of overexpression on differentiation of rat neural stem cells (NSCs) into neurons. Methods The RT-PCR was used to amplify rat BDNF gene from RNA of rat hippocampus. The BDNF gene was inserted into eukaryotic expression vector pEGFP-N1 to construct recombinant expression vector pEGFP-N1-BDNF. The recombinant vector was transfected into NSCs by Lipofectamine 2000.The expression of BDNF mRNA in NSCs was detected by RT-PCR. The differentiation of rat NSCs into neurons was detected by immunohistochemistry staining. Results The sequence of the cloned BDNF was confirmed to be correct by DNA sequencing. The NSCs transfected with pEGFP-N1-BDNF expressed BDNF efficiently. The pEGFP-N1-BDNF transfected NSCs differentiated into more neurons than the pEGFP-N1 transfected ones (EM>P/EM>0.01). Conclusion All these results indicate that BDNF overexpression significantly promotes the differentiation of rat NSCs

Key words: Brain-derived neurotrophic factor, Gene expression, Neural stem cell, Differentiation, RT-PCR, Immunohistochemistry, Rat

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