Fernandez-Castaneda Anthony, Gaultier Alban
Center for Brain Immunology and Glia, Department of Neuroscience, Graduate Program in Neuroscience, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Center for Brain Immunology and Glia, Department of Neuroscience, Graduate Program in Neuroscience, School of Medicine, University of Virginia, Charlottesville, VA 22908, USA.
Brain Behav Immun. 2016 Oct;57:1-7. doi: 10.1016/j.bbi.2016.01.005. Epub 2016 Jan 12.
Oligodendrocyte progenitor cells (OPCs) are the often-overlooked fourth glial cell type in the central nervous system (CNS), comprising about 5% of the CNS. For a long time, our vision of OPC function was limited to the generation of mature oligodendrocytes. However, new studies have highlighted the multifaceted nature of OPCs. During homeostatic and pathological conditions, OPCs are the most proliferative cell type in the CNS, a property not consistent with the need to generate new oligodendrocytes. Indeed, OPCs modulate neuronal activity and OPC depletion in the brain can trigger depressive-like behavior. More importantly, OPCs are actively recruited to injury sites, where they orchestrate glial scar formation and contribute to the immune response. The following is a comprehensive analysis of the literature on OPC function beyond myelination, in the context of the healthy and diseased adult CNS.
少突胶质前体细胞(OPCs)是中枢神经系统(CNS)中常被忽视的第四种神经胶质细胞类型,约占中枢神经系统的5%。长期以来,我们对少突胶质前体细胞功能的认识局限于其产生成熟少突胶质细胞的能力。然而,新的研究凸显了少突胶质前体细胞功能的多面性。在稳态和病理状态下,少突胶质前体细胞是中枢神经系统中增殖能力最强的细胞类型,这一特性与产生新的少突胶质细胞的需求并不相符。事实上,少突胶质前体细胞可调节神经元活动,大脑中少突胶质前体细胞的缺失会引发类似抑郁的行为。更重要的是,少突胶质前体细胞会被积极招募到损伤部位,在那里它们协调胶质瘢痕形成并参与免疫反应。以下是在健康和患病的成年中枢神经系统背景下,对少突胶质前体细胞髓鞘形成以外功能的文献进行的综合分析。