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作 者:熊南翔[1] 蒲建章[1] 赵洪洋[1] 苏群 姚东晓[1] 冯军[1]
机构地区:[1]华中科技大学同济医学院附属协和医院神经外科,武汉430022 [2]淄博市淄川医院内分泌科,淄博255100
出 处:《解剖学报》2007年第5期537-541,共5页Acta Anatomica Sinica
基 金:国家自然科学基金资助项目(30471775);湖北省科技攻关项目(2005AA301C15)
摘 要:目的研究Nogo-A基因沉默对PC12细胞多巴胺释放的影响。方法构建靶向Nogo-A的短发夹样RNA(shRNA)真核表达载体,并经脂质体转染PC12细胞,以逆转录聚合酶链反应(RT-PCR)和免疫印迹法检测对Nogo-A mRNA及蛋白的抑制效应。采用高效液相色谱仪(HPLC)检测转染前后多巴胺释放的变化。结果将重组质粒转染到PC12细胞48h后,Nogo-A基因表达明显受抑、多巴胺释放量减少。结论Nogo-A可能参与PC12细胞多巴胺的释放。Objective To study the effect of Nogo-A gene silence on dopamine release in PC12 cells. Methods The small hairpin RNA(shRNA) eukaryotic expression vector targeting Nogo-A gene was constructed and transfected into cultured PCI2 cells by lipofecamine2000. The inhibiting effect was detected by semi-quantitative reverse transcription(PCR) and Western blotting analysis. The dopamine release was detected by HPLC (high performance liquid chromatography) after transfection. Results The Nogo-A gene expression was inhibited and the dopamine release decresed significantly 48 hours after transfection. Conclusion The reasults suggest that Nogo-A be involved in the mechanism of dopamine realese in PC12 cells.
关 键 词:Nogo—A RNA干扰 PC12细胞 网状蛋白 逆转录聚合酶链反应
分 类 号:R322.81[医药卫生—人体解剖和组织胚胎学]
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