基础医学与临床 ›› 2011, Vol. 31 ›› Issue (3): 259-262.

• 研究论文 • 上一篇    下一篇

NEP1-40促进高苯丙氨酸损伤大鼠神经元Nogo A表达

黄成姣,黄丽素,张拥军,叶军,李端,顾学范   

  1. 上海交通大学医学院附属新华医院 上海市儿科医学研究所
  • 收稿日期:2009-11-03 修回日期:2010-07-28 出版日期:2011-03-05 发布日期:2011-03-14
  • 通讯作者: 顾学范 E-mail:GU Xu-fan(guxuefan@online.sh.cn
  • 基金资助:
    国家自然科学基金

NEP1-40 promoted expression of Nogo A in phenylalanine treated neuron

HUANG Cheng-jiao 1,HUANG Li-su 2,ZHANG Yong-jun 2,YE Jun 2,LI Duan 2,GU Xue-fan 1   

  1. 1. Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
    2.
  • Received:2009-11-03 Revised:2010-07-28 Online:2011-03-05 Published:2011-03-14
  • Contact: GU Xue-fan E-mail:GU Xu-fan(guxuefan@online.sh.cn

摘要: 目的 了解神经元NgR受体拮抗剂NEP1-40对高苯丙氨酸(Phe)作用下大鼠大脑皮质层神经元Nogo A蛋白表达的影响。方法 原代培养胎龄16~18天的SD大鼠皮质层神经元,体外模拟高Phe(0.9 mmol/L)环境,并用不同浓度NEP1-40干预;用免疫荧光方法检测神经元轴突生长和生长锥塌陷情况,实时荧光定量PCR和Western blot检测Nogo A mRNA和蛋白表达。结果 Nogo A可以在神经元胞体和突起表达;高Phe作用12、24和48h神经元Nogo A mRNA与alpha-tubulin (α-Tub,α微管蛋白)的相对表达量明显减低(P<0.05);高Phe作用后神经元Nogo A蛋白明显降低(P<0.05); NEP1-40对正常神经元无促进作用,但对高Phe时呈浓度依赖性地促进神经元Nogo A的表达。结论 NEP1-40可以促进高Phe损伤时神经元Nogo A的表达增高,从而促进神经元轴突的生长。

关键词: 高苯丙氨酸, 神经元, Nogo A, NEP1-40

Abstract: Objective Recently reasearch suggests that Nogo A expressed by oligodendrocytes and its receptor NgR may be involved in the etiology of neurophology of PKU or Hyperphenylalaninemia as an inhibitors, yet the action of Nogo A expressed by neuron is still not known. And whether its the specific antagonist to NgR (NEP1-40) can affect its expression. So the study was designed to investigate the effect by NEP1-40 on Nogo A in high phenyalanine(Phe) in vitro. Methods Cells was dissected from the cerebral cortex of E16~E18 embryos of SD rat, Real-time PCR and Western-Blot were used to evaluate the mRNA and protein of Nogo A respectively. The growth cones, axon and the Nogo A location were performed by immunofluorescence and immunohistochemistry respectively. Results Compared to the control, The mRNA and protein level of Nogo A with Phe for 12h, 24h and 48h were slightly reduced. NEP1-40 can upregulate expression of Nogo A on neuron in the high Phe condition with high level, but has no act on normal neuron. Conclusion NEP1-40 can promote expression of Nogo A on neuron in high Phe, which can help the neuron grow.

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