基础医学与临床 ›› 2007, Vol. 27 ›› Issue (12): 1334-1338.

• 研究论文 • 上一篇    下一篇

高表达人淀粉样前体蛋白降低SH-SY5Y细胞M胆碱受体结合

阮灿军 王抒 孙兰 杜冠华   

  1. 中国医学科学院基础医学研究所药理学系 协和医科大学基础医学院药理室 协和医科大学基础医学院药理室 中国医学科学院中国协和医科大学药物研究所
  • 收稿日期:2007-01-31 修回日期:2007-06-12 出版日期:2007-12-25 发布日期:2007-12-25
  • 通讯作者: 阮灿军

Over-expressed human amyloid precursor protein depressed M cholinergic receptor binding

Can-jun RUAN, Shu WANG, Lan SUN, Guan-hua DU   

  1. Institute of Basic Medical Sciences,CAMS & PUMC
  • Received:2007-01-31 Revised:2007-06-12 Online:2007-12-25 Published:2007-12-25
  • Contact: Can-jun RUAN,

摘要: 目的 观察阿尔茨海默病致病相关基因淀粉样前体蛋白(APP)基因的高表达致高度生成,对人神经母细胞瘤SH-SY5Y细胞的胆碱乙酰转移酶(ChAT)活性及M和N胆碱受体功能的影响,探讨β-样肽(Aβ)生成增加对细胞胆碱功能的作用。 方法 采用Lipofectamine 2000试剂盒将携带野生型人APP基因的pCMV695质粒转染至人神经母细胞瘤SH-SY5Y细胞中。以ELISA方法测定Aβ生成量。取稳定高表达Aβ细胞的克隆,用放射免疫法测定ChAT的活性;放射配基结合测定M、N乙酰胆碱受体结合。 结果 与未转染APP的SH-SY5Y细胞相比,当Aβ生成量为对照的2~2.6倍时SH-SY5Y-APP细胞中,未观察到明确的细胞毒性形态学改变;ChAT活性无明显变化,但细胞M受体结合降低18.5%~21.8 %(P<0.05);N受体结合未出现明显变化。结论 单纯Aβ产生增加就可通过影响M受体结合功能而引起脑内胆碱能功能障碍。

Abstract: Objective To observe the effect of over-expressed amyloid procursor protein (APP) gene, one of AD-related genes and overproduction of β-amyloid (Aβ) peptides, on the cholinergic receptor binding and the ChAT activity in human neuroblastoma cell line SH-SY5Y. METHODS SH-SY5Y cells were stably transfected with pCMV695 plasmid containing wild type human APP695 gene by Lipofectamine 2000 method. The expression of APP was detected by Western blot. Aβcontents were test by ELISA assay in over-expression SH-SY5Y cell clones (SH-SY5Y-APP). The special binding of muscarinic and nicotinic cholinergic receptors in those Aβ-overproducing cell clones were determined by radio-ligand binding method. The cholinergic acetyl transferase (ChAT) activity was assayed by radiao-immunoassay. RESULTS No evident morphologic changes of cytotoxicity were detected after transfection. When Aβproduction was 2~2.6 times as much as that of normal cells (i.e. it was below the concentrations of 115~150 pmol/L), muscarinic receptor binding was decreased from 18.5 % to 21.9 % (P<0.05) compared with normal cells. However, no marked alterations in nicotinic receptor binding and the ChAT activity were found. CONCLUSION In this experiment, we found that muscarinic receptor binding inhibition was showed before cytotoxicity, nicotinic receptor binding and ChAT activity changes in SH-SY5Y-APP. It is suggested that the increase of Aβproduction could independently caused the cholinergic dysfunction in early stage of AD brain tissues by muscarinic receptor binding inhibition.