ZHU Zhenzhong,HE Xijing,JIN Dongxu.Effect and mechanism of lithium on the differentiation of neural stem cells[J].Chinese Journal of Spine and Spinal Cord,2013,(12):1101-1108.
Effect and mechanism of lithium on the differentiation of neural stem cells
Received:January 04, 2013  Revised:June 18, 2013
English Keywords:Lithium  Neural stem cells  Differentiation
Fund:国家自然科学基金(项目编号:81200944/H0910);中国博士后基金(项目编号:2012M520044)
Author NameAffiliation
ZHU Zhenzhong Department of orthopedics, the Sixth People′s Hospital Affiliated to Shanghai Jiaotong University, Shanghai, 100035, China 
HE Xijing 西安交通大学第二附属医院骨科 710004 陕西省西安市 
JIN Dongxu 上海交通大学附属第六人民医院骨科 200233 上海市 
历 强  
张长青  
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English Abstract:
  【Abstract】 Objectives: To investigate the effect and its underlying mechanism of lithium on modulating neural stem cells differentiation. Methods: NSCs were isolated from the subventricular zone of neonatal Fischer 344 Rat. The growth curve of differentiating NSCs was detected by using Cyquant assay. Immunocytochemistry staining combining with BrdU incorporation assay were used to detectneuronal marker Tuj1 and astrocytes marker GFAP and S100β, the percentage, as well as the total numbers of each lineage were also estimated. TNUEL apoptosis assay was also performed to rule out the lithium toxicity. Finally, lithium and GSK3β inhibitor-SB216763′s effect on regulating neuraonal and astrocytes were tested and compared. Results: Lithium concentration lower than 3mM was non-toxic in differentiating NSCs. 1mM lithium stimulated neuronal production by 1.47±0.06 folds(P<0.05), while SB216763 increased by 2.25±0.07 folds(P<0.05), 3mM lithium reduced GFAP+ cell number to 0.55±0.02 folds(P<0.05) compared with control group, S100β staning result showed the similar tendency, conversely, SB216763 did not reduce GFAP+ cell number, with 0.90±0.06 folds compared with control group(P>0.05). Conclusions: Lithium exerts dual roles on NSCs′s differentiation. It stimulates neurogenesis at concentration of 1mM with its inhibition on doumregulating GSK3β pathway, meanwhile suppresses astrogliogenesis at concentration of 3mM, which may be mediated by non-canonical pathway.
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