首页> 外文期刊>Experimental Neurology >Recombinant adenovirus vector-mediated functional expression of neurotropin-3 receptor (TrkC) in neural stem cells.
【24h】

Recombinant adenovirus vector-mediated functional expression of neurotropin-3 receptor (TrkC) in neural stem cells.

机译:重组腺病毒载体介导的神经营养蛋白3受体(TrkC)在神经干细胞中的功能性表达。

获取原文
获取原文并翻译 | 示例
           

摘要

We have constructed a recombinant adenovirus expression vector carrying the human neurotrophin-3 (NT-3) receptor TrkC (tyrosine protein kinase C) gene (rAd-TrkC; 2478 bp) and confirmed the expression of the encoded TrkC in green fluorescent protein (GFP)-murine neural stem cells (NSCs) by reverse transcription polymerase chain reaction (RT-PCR), Western blot analysis, and immunocytochemistry. The activity of the expressed rAd-TrkC was verified in vitro by evaluating dose-related responses of NSCs to NT-3, a TrkC specific ligand. TrkC-GFP-NSCs had a significantly higher percentage of neuronal differentiation when treated with NT-3 relative to the rAd-LacZ control cells (55.2% vs. 29.8%; P<0.05, chi(2) test). Thus, our rAd-TrkC vector can transfect NSCs and produce functional TrkC receptors to promote neuronal differentiation of NSCs.
机译:我们已经构建了携带人神经营养蛋白3(NT-3)受体TrkC(酪氨酸蛋白激酶C)基因(rAd-TrkC; 2478 bp)的重组腺病毒表达载体,并证实了编码的TrkC在绿色荧光蛋白(GFP)中的表达鼠神经干细胞(NSC),通过逆转录聚合酶链反应(RT-PCR),蛋白质印迹分析和免疫细胞化学进行。表达的rAd-TrkC的活性在体外通过评估NSC对NT-3(一种TrkC特异性配体)的剂量相关反应进行验证。与rAd-LacZ对照细胞相比,用NT-3处理时,TrkC-GFP-NSC具有明显更高的神经元分化百分比(55.2%对29.8%; P <0.05,chi(2)测试)。因此,我们的rAd-TrkC载体可以转染NSC,并产生功能性TrkC受体,从而促进NSC的神经元分化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号