目的:改进少突胶质细胞体外培养方法。方法:取新生24 h内SD大鼠大脑皮质组织,采用机械性吸管吹打的方法获取细胞悬液,进行种植培养,恒温摇床结合无血清培养的方法纯化少突胶质细胞,Galc免疫细胞化学法鉴定少突胶质细胞。结果:纯化后的少突胶质细胞,胞体圆形或椭圆形,折光性强,突起少,经Galc免疫细胞化学染色,阳性细胞胞浆和突起呈棕黄色,少突胶质细胞纯度达95%。结论:采用此种方法培养出的少突胶质细胞纯化度高,且方便简易。
Objective: To improve the in vitro culture method for oligodendrocytes. Methods: Cells from cerebral cortex of 24 hours- old SD rats were disassociated by mechanical methods. Then,the cultured oligodendrocytes were purified using orbital shaker in constant temperature. The cultured oligodendrocytes were identified by immunocytochemical staining with anti- Galc antibody. Results: The purified oligodendrocytes showed round or oval cell body were and less cytoplasmic process. The cultured oligodendrocytes were identified by immunocytochemical staining with anti- Galc,which were stained brown in their cytoplasm and processes. The positive immunocytochemistry were counted more than 95 percents of all cells. Conclusion:The established method is simple,and the cultured oligodendrocytes is of high- grade purification.