体外少突胶质细胞培养的新方法

New Method for Oligodendrocyte Cell Culture in Vitro

目的探讨小鼠鼠婴大脑皮质体外少突胶质细胞培养的新方法。方法取C57/BL6新生小鼠P0~P2(出生后0~2天)的大脑皮质,accummax室温消化10min,然后用含10%FBS的DMEM/F-12高糖培养基体外培养,培养至第7天时,运用巴氏管吹打,从混合培养的细胞中分离纯化少突胶质前体细胞,然后加入促分化培养基促使少突胶质前体细胞分化发育成熟,行细胞免疫荧光进行鉴定。结果少突胶质前体细胞纯度较高,达到93.3%左右。加入促分化培养基后,少突胶质前体细胞可快速分化发育成熟。结论该体外少突胶质细胞培养方法较简单,细胞纯度及产量高,对临床脱髓鞘疾病的研究具有很大的应用价值。

Objective To explore a new method for oligodendrocyte cell culture from neonatal mouse cerebral cortex in vitro. Methods We selected PO - P2 （0 -2 days after birth） cerebral cortex from C57/BL6 neonatal mice, and digested the tissue at room temperature for 10 minutes through accummax, then used DMEM/F - 12 medium with high glucose containing 10% FBS to culture the mixed cells in vitro. After the celles being cultured for 7 days, we used pap tube for pipetting, and purified oligodendrocyte precursor cell （OPCs） from mixed cultured cells. Finally,with oligodendrocyte differentiation medium to promote oligodendrocyte differentiation and maturation, cell lines were identified by immunofluorescenee. Results Our approach produced a high yield of purified OPCs, which was about 93.3%. The oligodendrocyte differentiation medium promoted oligodendrocyte differentiation and maturation quickly, when it was added. Conclusion The new method for oligodendrocyte cell culture in vitro is relatively simple with high purity and can produce a high yield of OPCs, which is of great value for clinical demyelinated diseases.