Miller Robert H
Department of Neurosciences, School of Medicine, Case Western Reserve University E-721, 2109 Adelbert Road, Cleveland, OH 44106-4975, USA.
Prog Neurobiol. 2002 Aug;67(6):451-67. doi: 10.1016/s0301-0082(02)00058-8.
The vertebrate central nervous system (CNS) contains two major classes of macroglial cells, oligodendrocytes and astrocytes. Oligodendrocytes are responsible for the formation of myelin in the central nervous system, while the functions of astrocytes are more diverse and less well established. Recent studies have provided new insights into when, where and how these different classes of cell arise during CNS development. The founder cells of the oligodendrocyte lineage initially arise in distinct regions of the ventricular zone during early development as the result of local signals including sonic hedgehog. In the spinal cord, oligodendrocyte precursors appear to share a developmental lineage with motor neurons, although they may also develop from restricted glial precursors. Immature oligodendrocyte precursors are highly migratory. They migrate from their site of origin to developing white matter tracts using a variety of guidance cues including diffusible chemorepellents. The majority of oligodendrocyte precursor proliferation occurs in developing white matter as a result of the local expression of mitogenic signals. Oligodendrocyte precursor cell proliferation is regulated by a number of distinct growth factors that act at distinct stages in the lineage and whose activity is modulated by synergy with other molecules including chemokines. The final matching of oligodendrocyte and axon number is accomplished through a combination of local regulation of cell proliferation, differentiation and cell death. Not all oligodendrocyte precursors differentiate during development, and the adult CNS contains a significant population of precursors. Understanding the regulation of oligodendrogenesis will facilitate the use of these endogenous precursors to enhance repair in a variety of pathological conditions.
脊椎动物的中枢神经系统(CNS)包含两大类大胶质细胞,即少突胶质细胞和星形胶质细胞。少突胶质细胞负责中枢神经系统中髓磷脂的形成,而星形胶质细胞的功能则更为多样且尚未完全明确。最近的研究为这些不同类型的细胞在中枢神经系统发育过程中的产生时间、位置和方式提供了新的见解。少突胶质细胞谱系的起始细胞最初在早期发育过程中,由于包括音猬因子在内的局部信号,出现在脑室区的不同区域。在脊髓中,少突胶质细胞前体细胞似乎与运动神经元共享一个发育谱系,尽管它们也可能从有限的神经胶质前体细胞发育而来。未成熟的少突胶质细胞前体细胞具有高度迁移性。它们利用包括可扩散化学排斥剂在内的多种导向线索,从其起源部位迁移到正在发育的白质束。少突胶质细胞前体细胞的增殖大部分发生在正在发育的白质中,这是有丝分裂信号局部表达的结果。少突胶质细胞前体细胞的增殖受多种不同生长因子的调节,这些因子在谱系的不同阶段起作用,其活性通过与包括趋化因子在内的其他分子协同作用而受到调节。少突胶质细胞和轴突数量的最终匹配是通过细胞增殖、分化和细胞死亡的局部调节共同完成的。并非所有少突胶质细胞前体细胞在发育过程中都会分化,成年中枢神经系统中含有大量的前体细胞。了解少突胶质细胞生成的调节将有助于利用这些内源性前体细胞来促进各种病理状况下的修复。