Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, U.K.
MS Society Edinburgh Centre for MS Research, University of Edinburgh, Edinburgh, U.K.
Biosci Rep. 2024 Sep 25;44(9). doi: 10.1042/BSR20231616.
Myelination of axons is a key determinant of fast action potential propagation, axonal health and circuit function. Previously considered a static structure, it is now clear that myelin is dynamically regulated in response to neuronal activity in the central nervous system (CNS). However, how activity-dependent signals are conveyed to oligodendrocytes remains unclear. Here, we review the potential mechanisms by which neurons could communicate changing activity levels to myelin, with a focus on the accumulating body of evidence to support activity-dependent vesicular signalling directly onto myelin sheaths. We discuss recent in vivo findings of activity-dependent fusion of neurotransmitter vesicles from non-synaptic axonal sites, and how modulation of this vesicular fusion regulates the stability and growth of myelin sheaths. We also consider the potential mechanisms by which myelin could sense and respond to axon-derived signals to initiate remodelling, and the relevance of these adaptations for circuit function. We propose that axonal vesicular signalling represents an important and underappreciated mode of communication by which neurons can transmit activity-regulated signals to myelinating oligodendrocytes and, potentially, more broadly to other cell types in the CNS.
轴突髓鞘形成是快速动作电位传播、轴突健康和回路功能的关键决定因素。髓鞘先前被认为是一种静态结构,现在很清楚,它是中枢神经系统(CNS)神经元活动的响应下进行动态调节的。然而,活动依赖性信号如何被传递到少突胶质细胞仍然不清楚。在这里,我们回顾了神经元将不断变化的活动水平传递给髓鞘的潜在机制,重点介绍了越来越多的证据支持活动依赖性囊泡信号直接作用于髓鞘鞘上。我们讨论了最近在体发现的来自非突触轴突部位的神经递质囊泡的活动依赖性融合,以及这种囊泡融合的调节如何影响髓鞘鞘的稳定性和生长。我们还考虑了髓鞘感知和响应轴突衍生信号以启动重塑的潜在机制,以及这些适应性对于回路功能的相关性。我们提出,轴突囊泡信号代表了神经元向髓鞘形成少突胶质细胞传递活动调节信号的一种重要且未被充分认识的通讯方式,并且可能更广泛地传递给 CNS 中的其他细胞类型。
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