MRC Centre for Regenerative Medicine, MS Society Edinburgh Centre, University of Edinburgh, Edinburgh, United Kingdom.
Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Elife. 2019 Oct 28;8:e49493. doi: 10.7554/eLife.49493.
Experience and changes in neuronal activity can alter CNS myelination, but the signalling pathways responsible remain poorly understood. Here we define a pathway in which endothelin, signalling through the G protein-coupled receptor endothelin receptor B and PKC epsilon, regulates the number of myelin sheaths formed by individual oligodendrocytes in mouse and zebrafish. We show that this phenotype is also observed in the prefrontal cortex of mice following social isolation, and is associated with reduced expression of vascular endothelin. Additionally, we show that increasing endothelin signalling rescues this myelination defect caused by social isolation. Together, these results indicate that the vasculature responds to changes in neuronal activity associated with experience by regulating endothelin levels, which in turn affect the myelinating capacity of oligodendrocytes. This pathway may be employed to couple the metabolic support function of myelin to activity-dependent demand and also represents a novel mechanism for adaptive myelination.
神经元活动的经验和变化可以改变中枢神经系统的髓鞘形成,但负责的信号通路仍知之甚少。在这里,我们定义了一个途径,其中内皮素通过 G 蛋白偶联受体内皮素受体 B 和蛋白激酶 C epsilon 信号传导,调节单个少突胶质细胞形成的髓鞘鞘的数量在小鼠和斑马鱼中。我们表明,这种表型也在社交隔离后的小鼠前额叶皮层中观察到,并且与血管内皮素表达降低有关。此外,我们表明增加内皮素信号传导可以挽救社交隔离引起的这种髓鞘缺陷。总之,这些结果表明,血管系统通过调节内皮素水平来响应与经验相关的神经元活动变化,而内皮素水平反过来又影响少突胶质细胞的髓鞘形成能力。该途径可用于将髓鞘的代谢支持功能与活动依赖性需求联系起来,并且代表了一种用于适应性髓鞘形成的新机制。