Ono K, Kagawa T, Tsumori T, Yokota S, Yasui Y
Department of Anatomy, Second Division, Shimane Medical University, Izumo, Japan.
Dev Neurosci. 2001;23(4-5):346-55. doi: 10.1159/000048718.
Oligodendrocyte precursor cells (OPCs) originate in multiple restricted regions of the developing central nervous system (CNS). Here, we focus on morphological changes of oligodendrocyte lineage cells and their cellular dynamics including cell motility and proliferation. Morphological studies with molecular markers for OPCs suggest distinct spatiotemporal patterns of OPC migration in vivo, which are directly demonstrated by application of exogenous fluorescent markers to OPCs. Extensive proliferation of OPCs in the CNS parenchyma is also demonstrated by pulse labeling of the cells with bromodeoxyuridine. The results strongly suggest that oligodendrocyte lineage cells are highly motile and actively proliferate with an elongated morphology. These data provide insights into the potential molecular mechanisms of OPC dispersal throughout the CNS.
少突胶质前体细胞(OPCs)起源于发育中的中枢神经系统(CNS)的多个特定区域。在此,我们关注少突胶质细胞系细胞的形态变化及其细胞动力学,包括细胞运动性和增殖。使用OPCs分子标记的形态学研究表明,体内OPCs迁移具有独特的时空模式,通过对外源性荧光标记物应用于OPCs可直接证明这一点。用溴脱氧尿苷对细胞进行脉冲标记也证明了CNS实质中OPCs的广泛增殖。结果有力地表明,少突胶质细胞系细胞具有高度运动性,并以细长形态积极增殖。这些数据为OPCs在整个CNS中扩散的潜在分子机制提供了见解。