Centre for Neuroscience and Howard Florey Institutes, The University of Melbourne, Level 2, Alan Gilbert Building, 161 Barry Street, Carlton South, Victoria 3053, Australia.
Curr Opin Neurobiol. 2010 Oct;20(5):601-7. doi: 10.1016/j.conb.2010.05.005. Epub 2010 Jun 16.
The successful transduction of action potentials along vertebrate axons is highly reliant on myelin, the concentric layers of membrane surrounding most large diameter axons. Within the central nervous system myelin is produced by oligodendrocytes. Developmentally, the oligodendrocyte linage arises from subventricular zone progenitors that give rise to oligodendrocyte progenitor cells (OPCs), which divide and migrate throughout the CNS before terminally differentiating to generate mature oligodendrocytes which myelinate receptive axons. Each step of progression along the lineage is under tight transcriptional control, elucidation of this control is vital for understanding developmental myelination and for developing strategies to promote repair in demyelinating diseases. Recent studies have identified a number of new transcriptional regulators and microRNAs as having key roles in CNS myelination.
脊椎动物轴突上动作电位的成功传递高度依赖髓鞘,髓鞘是环绕大多数大直径轴突的同心膜层。在中枢神经系统中,髓鞘由少突胶质细胞产生。在发育过程中,少突胶质细胞谱系起源于室下区祖细胞,这些祖细胞产生少突胶质前体细胞(OPC),OPC 分裂并迁移到中枢神经系统的各个部位,然后终末分化为成熟的少突胶质细胞,后者对有髓轴突进行髓鞘化。沿谱系的每一步进展都受到严格的转录控制,阐明这种控制对于理解发育性髓鞘形成以及开发促进脱髓鞘疾病修复的策略至关重要。最近的研究已经确定了一些新的转录调节因子和 microRNAs,它们在中枢神经系统髓鞘形成中具有关键作用。