Institute of Neuronal Cell Biology, Technical University Munich , Munich, Germany.
German Center for Neurodegenerative Diseases , Munich, Germany.
J Cell Biol. 2023 Mar 6;222(3). doi: 10.1083/jcb.202204010. Epub 2023 Jan 13.
To enable rapid propagation of action potentials, axons are ensheathed by myelin, a multilayered insulating membrane formed by oligodendrocytes. Most of the myelin is generated early in development, resulting in the generation of long-lasting stable membrane structures. Here, we explored structural and dynamic changes in central nervous system myelin during development. To achieve this, we performed an ultrastructural analysis of mouse optic nerves by serial block face scanning electron microscopy (SBF-SEM) and confocal time-lapse imaging in the zebrafish spinal cord. We found that myelin undergoes extensive ultrastructural changes during early postnatal development. Myelin degeneration profiles were engulfed and phagocytosed by microglia using exposed phosphatidylserine as one "eat me" signal. In contrast, retractions of entire myelin sheaths occurred independently of microglia and involved uptake of myelin by the oligodendrocyte itself. Our findings show that the generation of myelin early in development is an inaccurate process associated with aberrant ultrastructural features that require substantial refinement.
为了实现动作电位的快速传播,轴突被髓鞘包裹,髓鞘是由少突胶质细胞形成的多层绝缘膜。髓鞘的大部分是在发育早期产生的,这导致了持久稳定的膜结构的产生。在这里,我们探索了中枢神经系统髓鞘在发育过程中的结构和动态变化。为了实现这一目标,我们通过连续块面扫描电子显微镜(SBF-SEM)对小鼠视神经进行了超微结构分析,并在斑马鱼脊髓中进行了共聚焦延时成像。我们发现,髓鞘在出生后早期发育过程中经历了广泛的超微结构变化。髓鞘退化的形态被小胶质细胞吞噬,利用暴露的磷脂酰丝氨酸作为一个“吃我”信号。相比之下,整个髓鞘鞘的回缩与小胶质细胞无关,涉及到少突胶质细胞自身对髓鞘的摄取。我们的研究结果表明,发育早期髓鞘的产生是一个不准确的过程,与异常的超微结构特征有关,需要进行大量的修正。