Department of Neurology, Stanford University, Stanford, CA, USA.
Howard Hughes Medical Institute, Stanford University, Stanford, CA, USA.
Nat Rev Neurol. 2022 Dec;18(12):735-746. doi: 10.1038/s41582-022-00737-3. Epub 2022 Nov 14.
Within the past decade, multiple lines of evidence have converged to identify a critical role for activity-regulated myelination in tuning the function of neural networks. In this Review, we provide an overview of accumulating evidence that activity-regulated myelination is required for brain adaptation and learning across multiple domains. We then discuss dysregulation of activity-dependent myelination in the context of neurological disease, a novel frontier with the potential to uncover new mechanisms of disease pathogenesis and to develop new therapeutic strategies. Alterations in myelination and neural network function can result from deficient myelin plasticity that impairs neurological function or from maladaptive myelination, in which intact activity-dependent myelination contributes to the disease process by promoting pathological patterns of neuronal activity. These emerging mechanisms suggest new avenues for therapeutic intervention that could more fully address the complex interactions between neurons and oligodendroglia.
在过去的十年中,多种证据表明,活性调节髓鞘形成在调节神经网络功能方面起着关键作用。在这篇综述中,我们提供了越来越多的证据,表明活性调节髓鞘形成是大脑适应和学习多个领域所必需的。然后,我们讨论了活性依赖的髓鞘形成失调在神经疾病中的情况,这是一个具有潜在发现疾病发病机制新机制和开发新治疗策略的新前沿。髓鞘形成和神经网络功能的改变可能是由于髓鞘可塑性不足导致的神经功能障碍,也可能是由于适应不良的髓鞘形成,其中完整的活性依赖的髓鞘形成通过促进神经元活动的病理模式而促进疾病过程。这些新出现的机制为治疗干预提供了新的途径,这可能更充分地解决神经元和少突胶质细胞之间的复杂相互作用。