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机构地区:[1]中国医科大学附属盛京医院神经内科,辽宁沈阳110004
出 处:《解剖科学进展》2014年第1期58-61,64,共5页Progress of Anatomical Sciences
基 金:辽宁省教育厅科学技术研究(No.2009A780);辽宁省博士科研启动基金(No.20091106);沈阳市科学技术计划(F1-262-9-20)
摘 要:目的探讨星形胶质细胞和1-甲基-4苯基-吡啶离子(MPP+)诱导的PC12细胞共育对神经干细胞(NSC)突触素和生长相关蛋白-43表达的影响。方法 PC12细胞分别经MPP+诱导不同时间点(0h、24h、48h、72h、96h)后分为两部分,一部分应用流式细胞技术检测PC12细胞凋亡率;另一部分与星形胶质细胞共育2d,然后收集各组细胞条件培养液,对神经干细胞进行诱导分化,免疫荧光检测神经干细胞突触素(SYN)和生长相关蛋白-43(GAP-43)表达。结果在MPP+作用48h时间点,PC12细胞凋亡率达高峰(P<0.05)。MPP+与PC12细胞和星形胶质细胞条件培养液共育48h可上调神经干细胞中突触素(A值=34.09±2.69)和GAP-43(A值=49.36±5.98)表达水平(P<0.05)。结论星形胶质细胞与MPP+诱导凋亡的PC12细胞共育后,促进神经干细胞突触素和GAP-43表达。Objective To study the effect of cocuhured 1-methyl-4 phenyl pyridinium(MPP + ) induced PC12 cells and astrocytes on the expression of synaptophysin and GAP-43 in neural stem cells of Wistar rat. Methods PC 12 cells and MPP + were cocuhured at different time(0h, 24h, 48h, 72h, 96h)as control, then the apoptosis rates of PC12 cells induced by MPP + were measured by Flowcytometer. MPP + and PC12 cells and astrocytes were incubated for 48 hours, then all cells-conditioned medium was collected and used to culture neural stem cells(NSCs). The expression of synaptophysin(SYN) and growth-associated protein-43(GAP-43) in NSCs of all groups were detected by immunofluorescence. Results The apoptosis rate of PC 12 cells induced by MPP + was the highest at 48h culture time, but lower at other culture hours( P 〈 0.05). The expression levels of synaptophysin(A value = 34.09 + 2.69) and GAP-43(A value = 49.36 _+ 5.98)in NSCs induced by astrocytes-conditioned medium cocultured for 48h were significantly upregulated compared to non astrocytes(P 〈0.05). Conclusion Coculture of astrocytes and MPP + and PC12 cells promotes the expression levels of synaptophysin and GAP-43 in NSCs.
关 键 词:星形胶质细胞 神经干细胞 突触素 生长相关蛋白-43 WISTAR大鼠
分 类 号:R322.81[医药卫生—人体解剖和组织胚胎学]
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