Qi Li, Tang Yonggang, He Wei, Pan Honghua, Jiang Wenxian, Wang Lin, Deng Weilin
Department of Neurology, The 181st Center Hospital of the People's Liberation Army, No. 1 Xin Qiao Yuan Rd., Guilin, 541002, Guangxi, China.
Cytotechnology. 2017 Apr;69(2):277-287. doi: 10.1007/s10616-016-0056-1. Epub 2017 Jan 24.
Parkinson's disease (PD) is one of the most common neural degenerative disease, affecting millions of people globally. Great progress has been made in the PD treatment, and one of the most promising one is the stem cell-based therapy. Thus, studies on the differentiation of neural stem cells (NSCs) are important to the advancement in PD therapy. In this study, we used the rat NSCs to elucidate the role of Lithium in the proliferation and differentiation of NSCs by immunostaining against Ki67 and BrdU analysis as well as immunostaining against specific neuronal markers. We concluded that lithium chloride (LiCl) treatment could enhance the proliferation in NSCs and promote the dopaminergic neuronal differentiation of NSCs in vitro. This process was potentially mediated by Wnt signaling pathway. Using the 6-OHDA-induced PD models, we provided evidence to show that LiCl had the capacity to enhance the proliferation in NSCs and differentiation towards dopaminergic neurons in vivo. The beneficial effect of LiCl treatment was further validated by the fact that the motor function as well as learning and memory was improved in the PD models through Rotarod test and Morris water maze analysis. The learning and memory improvement was further supported by the increase in dendrite spine density in PD models receiving LiCl-treated NSCs. Through this study, we concluded that Lithium plays an important role in promoting NSCs' neuronal differentiation in vitro and improving the symptoms of PD models in vivo. It is of great significance that this work showed the potential application of Lithium in the PD therapy in the future.
帕金森病(PD)是最常见的神经退行性疾病之一,全球数百万人受其影响。PD治疗已取得巨大进展,其中最有前景的治疗方法之一是基于干细胞的疗法。因此,神经干细胞(NSCs)分化的研究对PD治疗的进展至关重要。在本研究中,我们使用大鼠NSCs,通过针对Ki67的免疫染色和BrdU分析以及针对特定神经元标志物的免疫染色,阐明锂在NSCs增殖和分化中的作用。我们得出结论,氯化锂(LiCl)处理可增强NSCs的增殖,并在体外促进NSCs向多巴胺能神经元分化。这一过程可能由Wnt信号通路介导。使用6-OHDA诱导的PD模型,我们提供证据表明LiCl在体内具有增强NSCs增殖和向多巴胺能神经元分化的能力。通过转棒试验和莫里斯水迷宫分析,PD模型的运动功能以及学习和记忆得到改善,这进一步验证了LiCl治疗的有益效果。接受LiCl处理的NSCs的PD模型中树突棘密度增加,进一步支持了学习和记忆的改善。通过本研究,我们得出结论,锂在促进NSCs体外神经元分化和改善PD模型体内症状方面发挥重要作用。这项工作显示了锂在未来PD治疗中的潜在应用,具有重要意义。