Department of Biological Sciences, Dartmouth College, Hanover, New Hampshire.
Departments of Neurology and Neuroscience, Yale School of Medicine, New Haven, Connecticut.
Glia. 2019 Nov;67(11):2008-2019. doi: 10.1002/glia.23635. Epub 2019 Apr 29.
Myelin has traditionally been considered a static structure that is produced and assembled during early developmental stages. While this characterization is accurate in some contexts, recent studies have revealed that oligodendrocyte generation and patterns of myelination are dynamic and potentially modifiable throughout life. Unique structural and biochemical properties of the myelin sheath provide opportunities for the development and implementation of multimodal label-free and fluorescence optical imaging approaches. When combined with genetically encoded fluorescent tags targeted to distinct cells and subcellular structures, these techniques offer a powerful methodological toolbox for uncovering mechanisms of myelin generation and plasticity in the live brain. Here, we discuss recent advances in these approaches that have allowed the discovery of several forms of myelin plasticity in developing and adult nervous systems. Using these techniques, long-standing questions related to myelin generation, remodeling, and degeneration can now be addressed.
髓鞘传统上被认为是一种静态结构,它在早期发育阶段产生和组装。虽然这种特征在某些情况下是准确的,但最近的研究表明,少突胶质细胞的产生和髓鞘形成的模式是动态的,并在整个生命周期中具有潜在的可修饰性。髓鞘独特的结构和生化特性为开发和实施多模态无标记和荧光光学成像方法提供了机会。当与针对不同细胞和亚细胞结构的遗传编码荧光标记物结合使用时,这些技术为揭示活脑中髓鞘生成和可塑性的机制提供了强大的方法工具箱。在这里,我们讨论了这些方法的最新进展,这些进展使得在发育和成人神经系统中发现了几种形式的髓鞘可塑性。使用这些技术,现在可以解决与髓鞘生成、重塑和退化相关的长期问题。