【摘要】 目的探讨b-FGF壳聚糖载体(Chitosan carrier)缓释对神经干细胞分化为神经元的作用。方法原代培养和鉴定神经干细胞,随机分为b-FGF壳聚糖缓释组,壳聚糖对照组和b-FGF对照组,Image-pro Plus 2. 0图像分析软件测量细胞突起长度,免疫组织化学方法检测分化细胞中NSE阳性细胞比例,Western blot法检测分化细胞中βⅢ-tubulin的表达和Akt磷酸化程度。结果 48h诱导后,诱导壳聚糖对照组、b-FGF对照组和b-FGF壳聚糖缓释组神经元的分化率分别为38. 5%、42. 6%和70. 8%。b-FGF壳聚糖缓释组与壳聚糖对照组神经元分化率上升(P <0. 05),b-FGF壳聚糖缓释组与b-FGF对照组相比神经元分化率显著提高(P <0. 05);诱导48h后,b-FGF壳聚糖缓释组与壳聚糖对照组和b-FGF对照组相比,神经元突起长度均出现显著增长,差异有统计学意义(P <0. 05); b-FGF壳聚糖缓释组与壳聚糖对照组和b-FGF对照组相比βⅢ-tubulin表达显著增加(P <0.05);诱导5、15和30min后,与b-FGF对照组相比,b-FGF壳聚糖缓释组Akt磷酸化水平显著升高,差异有统计学意义(P <0. 05)。结论 b-FGF经壳聚糖载体缓释后诱导神经元突起形成,提高神经元分化率,Akt磷酸化激活的信号途径可能参与b-FGF壳聚糖载体诱导神经干细胞过程神经元分化速度的调节。更多还原

【Abstract】 Objective To investigate the effects of b-FGF on the differentiation and formation of neurons from neural stem cells were investigated by Chitosan carrier. Methods The cultured neural stem cells by primary sources,the experiment was divided into b-FGF sustained-releasing chitosan group,chitosan control group and b-FGF control group. Affect the measurement of Chitosan differentiation group and b-FGF differentiation group and Chitosan sustained-releasing groups of the neurite formation,using image analysis software Image-pro Plus2. 0 image analysis software to measure cell neurite length in data acquisition. Immunohistochemical method was to check cell differentiation the ratio of NSE positive cells. Western blot method was performed to detect the expression of Akt phosphorylation. Results The induction of differentiation of neural stem cells into neuronal differentiation rate were 38. 5%(Chitosan group),42. 6%( b-FGF group)and 70. 8%(b-FGF Chitosan sustained-releasing group),the differentiation rate of neurons in b-FGF chitosan sustained-releasing group was higher than that in the chitosan control group(P < 0. 05),and the differentiation rate of neurons in b-FGF chitosan sustained-releasing group was higher than that in b-FGF control group(P < 0. 05);48 hours after induction,the neurite length of the b-FGF chitosan sustained-releasing group increased compared with that in the chitosan control group and the b-FGF control group,and the difference was statistically significant(P < 0. 05);The expression of βⅢ-tubulin was increased in b-FGF chitosan sustainedreleasing group compared with chitosan control group and b-FGF control group(P < 0. 05);After 5 minutes,15 minutes and 30 minutes of induction,the phosphorylation level of Akt in b-FGF chitosan sustainedreleasing group was higher than that in b-FGF control group,and the difference was statistically significant(P< 0. 05). Conclusion B-FGF could induce neurite formation and increase the differentiation rate of neurons after sustained release by chitosan carrier. Akt phosphorylation-activated signaling pathway may be involved in the regulation of neuronal differentiation rate in the process of b-FGF chitosan vector-induced neural stem cells.更多还原