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小鼠小脑白质发育过程中单个少突胶质细胞髓鞘形成的轴突选择性

Axonal Selectivity of Myelination by Single Oligodendrocytes Established During Development in Mouse Cerebellar White Matter.

作者信息

Battulga Batpurev, Osanai Yasuyuki, Yamazaki Reiji, Shinohara Yoshiaki, Ohno Nobuhiko

机构信息

Division of Histology and Cell Biology, Department of Anatomy, School of Medicine, Jichi Medical University, Shimotsuke, Japan.

Department of Anatomy and Systems Biology, Faculty of Medicine, University of Yamanashi, Chuo, Japan.

出版信息

Glia. 2025 Apr;73(4):873-886. doi: 10.1002/glia.24660. Epub 2024 Dec 17.

Abstract

Myelin formation by oligodendrocytes regulates the conduction velocity and functional integrity of neuronal axons. While individual oligodendrocytes form myelin sheaths around multiple axons and control the functions of neural circuits where the axons are involved, it remains unclear if oligodendrocytes selectively form myelin sheaths around specific subtypes of axons. Using the combination of rabies virus-mediated single oligodendrocyte labeling and immunostaining with tissue clearing, we revealed that approximately half of the oligodendrocytes preferentially myelinate axons originating from Purkinje cells in the white matter of adult mouse cerebella. The preference for Purkinje cell axons was more pronounced during development when the process of myelination within cerebellar white matter was initiated; over 90% of oligodendrocytes preferentially myelinated Purkinje cell axons. Preferential myelination of Purkinje cell axons was further confirmed by immuno-electron microscopy and transgenic mice that label early-born oligodendrocytes. Transgenic mice that label oligodendrocytes differentiated at the early development showed that early-born oligodendrocytes preferentially myelinate Purkinje cell axons in the matured cerebellar white matter. In contrast, transgenic mice that label oligodendrocytes differentiated after the peak of cerebellar myelination showed that the later-differentiated oligodendrocytes dominantly myelinated non-Purkinje cell axons. These results demonstrate that a significant proportion of oligodendrocytes preferentially myelinate functionally distinct axons in the cerebellar white matter, and the axonal preference of myelination by individual oligodendrocytes is established depending on the timing of their differentiation during development. Our data provide the evidence that there is a critical time window of myelination that a specific subtype of axons are dominantly myelinated by the oligodendrocytes.

摘要

少突胶质细胞形成的髓鞘调节神经元轴突的传导速度和功能完整性。虽然单个少突胶质细胞会在多条轴突周围形成髓鞘,并控制轴突所涉及的神经回路的功能,但尚不清楚少突胶质细胞是否会选择性地在特定亚型的轴突周围形成髓鞘。通过狂犬病病毒介导的单个少突胶质细胞标记与组织透明化免疫染色相结合的方法,我们发现约一半的少突胶质细胞优先为成年小鼠小脑白质中源自浦肯野细胞的轴突形成髓鞘。在小脑白质髓鞘形成过程开始的发育阶段,对浦肯野细胞轴突的偏好更为明显;超过90%的少突胶质细胞优先为浦肯野细胞轴突形成髓鞘。免疫电子显微镜和标记早期生成的少突胶质细胞的转基因小鼠进一步证实了浦肯野细胞轴突的优先髓鞘形成。标记在早期发育阶段分化的少突胶质细胞的转基因小鼠表明,早期生成的少突胶质细胞在成熟的小脑白质中优先为浦肯野细胞轴突形成髓鞘。相比之下,标记在小脑髓鞘形成高峰期之后分化的少突胶质细胞的转基因小鼠表明,后期分化的少突胶质细胞主要为非浦肯野细胞轴突形成髓鞘。这些结果表明,相当一部分少突胶质细胞优先为小脑白质中功能不同的轴突形成髓鞘,并且单个少突胶质细胞髓鞘形成的轴突偏好是根据其在发育过程中的分化时间确定的。我们的数据提供了证据,表明存在一个关键的髓鞘形成时间窗口,在这个窗口内特定亚型的轴突主要由少突胶质细胞形成髓鞘。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f42c/11845844/745366e4d831/GLIA-73-873-g005.jpg

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