Department of Biology and Center for Cell Reprogramming, Georgetown University, Washington, DC, 20057, USA.
Interdisciplinary Program in Neuroscience, Georgetown University, Washington, DC, 20057, USA.
Neurochem Res. 2020 Mar;45(3):630-642. doi: 10.1007/s11064-020-02967-7. Epub 2020 Jan 29.
Oligodendrocytes (OLs) generate myelin membranes for the rapid propagation of electrical signals along axons in the central nervous system (CNS) and provide metabolites to support axonal integrity and function. Differentiation of OLs from oligodendrocyte progenitor cells (OPCs) is orchestrated by a multitude of intrinsic and extrinsic factors in the CNS. Disruption of this process, or OL loss in the developing or adult brain, as observed in various neurological conditions including hypoxia/ischemia, stroke, and demyelination, results in axonal dystrophy, neuronal dysfunction, and severe neurological impairments. While much is known regarding the intrinsic regulatory signals required for OL lineage cell progression in development, studies from pathological conditions highlight the importance of the CNS environment and external signals in regulating OL genesis and maturation. Here, we review the recent findings in OL biology in the context of the CNS physiological and pathological conditions, focusing on extrinsic factors that facilitate OL development and regeneration.
少突胶质细胞(OLs)在中枢神经系统(CNS)中为轴突上的电信号的快速传播生成髓鞘膜,并提供代谢物以支持轴突的完整性和功能。OLs 由 CNS 中的多种内在和外在因素从少突胶质前体细胞(OPCs)分化而来。该过程的中断,或在发育中和成年脑中的 OL 丢失,如在包括缺氧/缺血、中风和脱髓鞘在内的各种神经疾病中观察到的那样,导致轴突营养不良、神经元功能障碍和严重的神经损伤。虽然在发育过程中 OL 谱系细胞进展所需的内在调节信号方面有很多了解,但来自病理条件的研究强调了 CNS 环境和外部信号在调节 OL 发生和成熟方面的重要性。在这里,我们根据 CNS 的生理和病理条件,综述 OL 生物学的最新发现,重点介绍促进 OL 发育和再生的外在因素。