摘要
目的对少突胶质前体细胞(OPCs)的分离、培养及传代方法进行改良,并建立少突胶质谱系限制细胞的体外分化模型,以模拟体内OPCs的发育过程。方法通过非特异性差异黏附法与A2B5-IgM抗体免疫筛选法结合,从胚胎大鼠脊髓来源的细胞悬液中分离、纯化OPCs,用含成纤维细胞生长因子-2和血小板源性生长因子的培养液作扩增培养;再以三碘甲状腺氨酸和神经营养因子-3诱导OPCs分化,最终分化为成熟的少突胶质细胞(OLs)。OPCs及其分化细胞的特性通过形态学观察和免疫化学染色法鉴定。结果 95%以上的细胞具有双极或三极突起的典型OPCs形态,并表达A2B5;在一定的培养条件下,OPCs可持续扩增和反复传代,且扩增的OPCs仍能维持其特有的形态和自我增殖的特性;进入分化进程的细胞将依次表达O4、O1、受体反应蛋白及髓鞘碱性蛋白等特异性分化抗原。结论分离的OPCs在形态、增殖以及分化格局等方面均与存在于胚胎脑区的O2A前体细胞(体内OPCs)相类似。
Objective To obtain healthier and purer oligodendrocyte precursor cells(OPCs) via modification of the methods in OPCs isolation,culture and generation passage,and to mimic the development of OPCs in vivo via setup of an in vitro model of lineage restricted oligodendrocyte differentiation. MethodsUsing nonspecific differentiated pre-attachment and A2B5-IgM immuno-panning,OPCs isolated from embryonic rat spinal cords were highly purified.Their proliferations were induced by enrichment of the culture solution with fibroblast growth factor-2 and platelet-derived growth factor,and their differentiations to mature oligodendrocytes were induced with tri-iodothyronine and neurotrophin-3.The morphology and characteristics of OPCs and cells differentiated from them were observed using microscope and immunostaining. ResultsMore than 95% of the cells exhibited typical OPCs morphology of bipolar or tripolar processes,and expressed A2B5.These cells could proliferate steadily and execute generation passage repeatedly.After inducement into differentiation process,cells expressed specific antigens,such as O4,O1,receptor-interacting protein and myelin basic protein,sequentially. ConclusionThe morphology,proliferation and differentiation of the isolated OPCs are similar with the O2A precursor cells in embryonic brain(natural OPCs).
出处
《上海交通大学学报（医学版）》
CAS
CSCD
北大核心
2011年第10期1500-1504,共5页
Journal of Shanghai Jiao tong University:Medical Science
基金
上海市教委基金(06BZ006)
上海交通大学基础医学院青年教师科研能力提升计划~~
