Almeida Rafael G, Lyons David A
Centre for Discovery Brain Sciences,
MS Society Centre for Translational Research, and.
J Neurosci. 2017 Oct 18;37(42):10023-10034. doi: 10.1523/JNEUROSCI.3185-16.2017.
Studies of activity-driven nervous system plasticity have primarily focused on the gray matter. However, MRI-based imaging studies have shown that white matter, primarily composed of myelinated axons, can also be dynamically regulated by activity of the healthy brain. Myelination in the CNS is an ongoing process that starts around birth and continues throughout life. Myelin in the CNS is generated by oligodendrocytes and recent evidence has shown that many aspects of oligodendrocyte development and myelination can be modulated by extrinsic signals including neuronal activity. Because modulation of myelin can, in turn, affect several aspects of conduction, the concept has emerged that activity-regulated myelination represents an important form of nervous system plasticity. Here we review our increasing understanding of how neuronal activity regulates oligodendrocytes and myelinated axons , with a focus on the timing of relevant processes. We highlight the observations that neuronal activity can rapidly tune axonal diameter, promote re-entry of oligodendrocyte progenitor cells into the cell cycle, or drive their direct differentiation into oligodendrocytes. We suggest that activity-regulated myelin formation and remodeling that significantly change axonal conduction properties are most likely to occur over timescales of days to weeks. Finally, we propose that precise fine-tuning of conduction along already-myelinated axons may also be mediated by alterations to the axon itself. We conclude that future studies need to analyze activity-driven adaptations to both axons and their myelin sheaths to fully understand how myelinated axon plasticity contributes to neuronal circuit formation and function.
对活动驱动的神经系统可塑性的研究主要集中在灰质上。然而,基于磁共振成像的研究表明,主要由有髓轴突组成的白质也可受到健康大脑活动的动态调节。中枢神经系统中的髓鞘形成是一个持续的过程,始于出生前后并贯穿一生。中枢神经系统中的髓鞘由少突胶质细胞产生,最近的证据表明,少突胶质细胞发育和髓鞘形成的许多方面可受到包括神经元活动在内的外在信号的调节。由于髓鞘的调节反过来又会影响传导的多个方面,因此出现了这样的概念,即活动调节的髓鞘形成代表了神经系统可塑性的一种重要形式。在此,我们综述了我们对神经元活动如何调节少突胶质细胞和有髓轴突的日益深入的理解,重点关注相关过程的时间安排。我们强调了这些观察结果:神经元活动可迅速调整轴突直径,促进少突胶质细胞前体细胞重新进入细胞周期,或驱动它们直接分化为少突胶质细胞。我们认为,显著改变轴突传导特性的活动调节的髓鞘形成和重塑最有可能在数天至数周的时间尺度上发生。最后,我们提出,沿已髓鞘化轴突的传导的精确微调也可能由轴突本身的改变介导。我们得出结论,未来的研究需要分析活动驱动的对轴突及其髓鞘的适应性变化,以全面了解有髓轴突可塑性如何促进神经元回路的形成和功能。