Zilkha Neurogenetic Institute, Department of Biochemistry and Molecular Biology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA.
J Cell Biol. 2010 Feb 8;188(3):305-12. doi: 10.1083/jcb.200905111.
The development and maturation of the oligodendrocyte requires a series of highly orchestrated events that coordinate the proliferation and differentiation of the oligodendrocyte precursor cell (OPC) as well as the spatiotemporal regulation of myelination. In recent years, widespread interest has been devoted to the therapeutic potential of adult OPCs scattered throughout the central nervous system (CNS). In this review, we highlight molecular mechanisms controlling OPC differentiation during development and the implication of these mechanisms on adult OPCs for remyelination. Cell-autonomous regulators of differentiation and the heterogeneous microenvironment of the developing and the adult CNS may provide coordinated inhibitory cues that ultimately maintain a reservoir of uncommitted glia.
少突胶质细胞的发育和成熟需要一系列高度协调的事件,这些事件协调少突胶质前体细胞(OPC)的增殖和分化,以及髓鞘形成的时空调节。近年来,人们广泛关注散布在中枢神经系统(CNS)中的成年 OPC 的治疗潜力。在这篇综述中,我们强调了控制发育过程中 OPC 分化的分子机制,以及这些机制对成年 OPC 进行髓鞘再生的意义。分化的细胞自主调节剂和发育中和成年 CNS 的异质微环境可能提供协调的抑制信号,最终维持未分化胶质细胞的储备。