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少突胶质细胞死亡启动同步髓鞘再生,以恢复小鼠大脑皮质的髓鞘模式。

Oligodendrocyte death initiates synchronous remyelination to restore cortical myelin patterns in mice.

机构信息

Department of Biological Sciences, Dartmouth College, Hanover, NH, USA.

出版信息

Nat Neurosci. 2023 Apr;26(4):555-569. doi: 10.1038/s41593-023-01271-1. Epub 2023 Mar 16.

Abstract

Myelin degeneration occurs in neurodegenerative diseases and aging. In these conditions, resident oligodendrocyte progenitor cells (OPCs) differentiate into oligodendrocytes that carry out myelin repair. To investigate the cellular dynamics underlying these events, we developed a noninflammatory demyelination model that combines intravital two-photon imaging with a single-cell ablation technique called two-photon apoptotic targeted ablation (2Phatal). Oligodendrocyte 2Phatal in both sexes results in a myelin degeneration cascade that triggers rapid forms of synchronous remyelination on defined axons. This remyelination is driven by oligodendrocytes differentiated from a subset of morphologically distinct, highly branched OPCs. Moreover, remyelination efficiency depends on the initial myelin patterns, as well as the age of the organism. In summary, using 2Phatal, we show a form of rapid synchronous remyelination, mediated by a distinct subset of OPCs, capable of restoring the original myelin patterning in adulthood but not aging.

摘要

髓鞘退化发生在神经退行性疾病和衰老中。在这些情况下,常驻少突胶质前体细胞(OPC)分化为少突胶质细胞,从而进行髓鞘修复。为了研究这些事件背后的细胞动态,我们开发了一种非炎症性脱髓鞘模型,该模型结合了活体双光子成像和一种称为双光子凋亡靶向消融(2Phatal)的单细胞消融技术。在两性中对少突胶质细胞进行 2Phatal 处理会导致髓鞘退化级联反应,从而迅速触发特定轴突上的同步髓鞘再生。这种髓鞘再生是由从形态上明显不同的高度分支 OPC 亚群分化而来的少突胶质细胞驱动的。此外,髓鞘再生效率取决于初始髓鞘模式以及生物体的年龄。总之,我们使用 2Phatal 显示了一种快速的同步髓鞘再生形式,由一组形态独特的高度分支的 OPC 介导,能够在成年期恢复原始的髓鞘模式,但不能恢复衰老。

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