›› 2008, Vol. 39 ›› Issue (2): 155-159.doi:

• 论著 • 上一篇    下一篇

Erk信号途径在B104 CM诱导神经干细胞向少突胶质细胞前体分化中的作用

胡建国1*; 钟政荣1;王凤超1;富赛里2;陆佩华2   

  1. 1.蚌埠医学院附属医院检验科,蚌埠 233004; 2.上海交通大学医学院神经生物学实验室,上海 200025
  • 收稿日期:2007-03-01 修回日期:2007-04-09 出版日期:2008-04-06
  • 通讯作者: 胡建国

THE ROLE OF Erk SIGNAL PATHWAY IN B104 CMINDUCED OPC DIFFERENTIATION FROM NSCs

  1. 1.Department of Laboratory, the Affiliated Hospital of Bengbu Medical College, Bengbu 233000,China;2.Department of Neurobiology, School of Medicine Shanghai Jiaotong University, Shanghai 200025,China
  • Received:2007-03-01 Revised:2007-04-09 Online:2008-04-06
  • Contact: HU Jian-guo

关键词: 神经母细胞瘤B104细胞系来源的条件培养基, 神经干细胞, 少突胶质细胞前体, 分化, 细胞外信号调节激酶, 免疫印迹法, 逆转录聚合酶链反应, 大鼠

Abstract: Objective To investigate the role of extracellular signalregulated kinase (Erk) and transcriptional factors such as c-fos, c-jun in B104 CMinduced oligodendrocyte progenitor cells (OPCs) differentiation from neural stem cells (NSCs). Methods The effect of U0126, the specific inhibitor of Erk1/2, on B104 CM induced OPC differentiation from NSCs was observed by morphology. The phosphorylation of Erk1/2 and mRNA expression of transcriptional factors c-fos, c-jun and c-myc in NSCs in the control group, B104 CM treated group and U0126 preincubated group were detected by Western blotting and RT-PCR methods respectively. Results B104 CMinduced OPC differentiation from NSCs could be blocked by preincubation of U0126 Treatment of NSCs with B104 CM produced a rapid increase in phosphorylation of Erk1/2 and an upregulation of c-fos andc-jun mRNA expression, which could be blocked by the preincubation of U0126 Conclusion B104 CM instructs oligodendrocyte differentiation from NSCs through the activ

Key words: B104 CM, NSCs, OPCs, Differentiation, Erk, Western blotting, RT-PCR, Rat

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