生存还是毁灭:在发育期间和中枢神经系统创伤后驱动髓磷脂形成的环境因素

Nicole Pukos, R. Yoseph, Dana M. McTigue
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引用次数: 7

摘要

少突胶质细胞是一种专门的神经胶质细胞,为中枢神经系统(CNS)轴突提供髓鞘。历史上,人们认为髓磷脂的主要作用是紧密包裹轴突,为快速信号传导提供必要的绝缘。然而,越来越多的证据证明了髓鞘和少突胶质细胞的动态重要性,包括为神经元提供代谢支持和调节轴突蛋白分布。因此,少突胶质细胞和髓鞘的发育和维持对于保持中枢神经系统稳态和支持广泛神经网络的正常功能是不可或缺的。环境信号对于适当的少突胶质细胞谱系细胞进展及其形成功能性致密髓鞘的能力至关重要;这些信号明显受到中枢神经系统损伤的干扰,这可能损害内源性髓鞘修复能力。这篇综述概述了在发育过程中驱动髓鞘形成的一些关键环境因素,并将其与定义中枢神经系统损伤环境的主要因素进行了比较。我们的目的是确定中枢神经系统创伤后被破坏的发育因子以及对少突胶质细胞谱系细胞产生负面影响的致病因子,因为这些是促进损伤或疾病后髓鞘修复的潜在治疗靶点。
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To Be or Not to Be: Environmental Factors that Drive Myelin Formation during Development and after CNS Trauma
Oligodendrocytes are specialized glial cells that myelinate central nervous system (CNS) axons. Historically, it was believed that the primary role of myelin was to compactly ensheath axons, providing the insulation necessary for rapid signal conduction. However, mounting evidence demonstrates the dynamic importance of myelin and oligodendrocytes, including providing metabolic support to neurons and regulating axon protein distribution. As such, the development and maintenance of oligodendrocytes and myelin are integral to preserving CNS homeostasis and supporting proper functioning of widespread neural networks. Environmental signals are critical for proper oligodendrocyte lineage cell progression and their capacity to form functional compact myelin; these signals are markedly disturbed by injury to the CNS, which may compromise endogenous myelin repair capabilities. This review outlines some key environmental factors that drive myelin formation during development and compares that to the primary factors that define a CNS injury milieu. We aim to identify developmental factors disrupted after CNS trauma as well as pathogenic factors that negatively impact oligodendrocyte lineage cells, as these are potential therapeutic targets to promote myelin repair after injury or disease.
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