Zhang S C, Lipsitz D, Duncan I D
Department of Medical Sciences, School of Veterinary Medicine, University of Wisconsin-Madison, 53706, USA.
J Neurosci Res. 1998 Oct 15;54(2):181-90. doi: 10.1002/(SICI)1097-4547(19981015)54:2<181::AID-JNR6>3.0.CO;2-A.
We have previously shown that oligodendroglial progenitors (OP) can be generated from multipotent rat neural precursor cells. We now report the generation of a homogeneous culture of canine OP from neural precursor cells. In non-adherent cultures, homogeneous OP cultures were obtained in 6-8 weeks of treatment with B104 cell conditioned medium (B104CM). In adherent cultures where astrocytes grew as a layer of substrate, colonies of OP invariably appeared at 10-14 days in vitro (DIV) and the colonies were expanded as free-floating spheres (oligospheres), in the presence of B104CM, suggesting that astrocytes facilitate the generation of canine OP. The oligosphere cells were characterized by self-renewal in the presence of B104CM and by terminal differentiation into oligodendrocytes after withdrawal of B104CM. Transplantation studies indicated that the extensively expanded oligosphere cells retained myelination capacity. The oligospheres thus provide a valuable source for experimental cell therapy studies.
我们之前已经表明,少突胶质前体细胞(OP)可由多能大鼠神经前体细胞产生。我们现在报告从神经前体细胞生成犬类OP的同质培养物。在非贴壁培养中,用B104细胞条件培养基(B104CM)处理6 - 8周可获得同质的OP培养物。在星形胶质细胞作为底物层生长的贴壁培养中,OP集落总是在体外培养10 - 14天(DIV)时出现,并且在B104CM存在的情况下,这些集落会扩展为自由漂浮的球体(少突球),这表明星形胶质细胞促进犬类OP的产生。少突球细胞的特征是在B104CM存在下自我更新,在去除B104CM后终末分化为少突胶质细胞。移植研究表明,广泛扩增的少突球细胞保留了髓鞘形成能力。因此,少突球为实验性细胞治疗研究提供了宝贵的来源。