Mitew S, Hay C M, Peckham H, Xiao J, Koenning M, Emery B
Department of Anatomy and Neuroscience, The University of Melbourne, Australia.
Department of Anatomy and Neuroscience, The University of Melbourne, Australia; Florey Institute of Neuroscience and Mental Health, The University of Melbourne, Australia.
Neuroscience. 2014 Sep 12;276:29-47. doi: 10.1016/j.neuroscience.2013.11.029. Epub 2013 Nov 22.
Oligodendrocytes and the myelin they produce are a remarkable vertebrate specialization that enables rapid and efficient nerve conduction within the central nervous system. The generation of myelin during development involves a finely-tuned pathway of oligodendrocyte precursor specification, proliferation and migration followed by differentiation and the subsequent myelination of appropriate axons. In this review we summarize the molecular mechanisms known to regulate each of these processes, including the extracellular ligands that promote or inhibit development of the oligodendrocyte lineage, the intracellular pathways they signal through and the key transcription factors that mediate their effects. Many of these regulatory mechanisms have recurring roles in regulating several transitions during oligodendrocyte development, highlighting their importance. It is also highly likely that many of these developmental mechanisms will also be involved in myelin repair in human neurological disease.
少突胶质细胞及其产生的髓鞘是脊椎动物的一项非凡特化,它能使中枢神经系统内实现快速且高效的神经传导。发育过程中髓鞘的生成涉及一条精细调节的途径,即少突胶质细胞前体的特化、增殖和迁移,随后是分化以及对合适轴突的髓鞘形成。在本综述中,我们总结了已知调控这些过程中每一个过程的分子机制,包括促进或抑制少突胶质细胞谱系发育的细胞外配体、它们通过其发出信号的细胞内途径以及介导其作用的关键转录因子。这些调控机制中的许多在调节少突胶质细胞发育过程中的多个转变方面反复发挥作用,凸显了它们的重要性。而且很有可能这些发育机制中的许多也会参与人类神经疾病中的髓鞘修复。