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早期髓鞘形成涉及轴突的动态和重复包绕,通过低而稳定的稳定化速率来解决。

Early myelination involves the dynamic and repetitive ensheathment of axons which resolves through a low and consistent stabilization rate.

机构信息

Department of Cell and Developmental Biology, University of Colorado School of Medicine, Aurora, United States.

出版信息

Elife. 2023 Apr 20;12:e82111. doi: 10.7554/eLife.82111.

DOI:10.7554/eLife.82111
PMID:37078701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10198724/
Abstract

Oligodendrocytes in the central nervous system exhibit significant variability in the number of myelin sheaths that are supported by each cell, ranging from 1 to 50 (1-8). Myelin production during development is dynamic and involves both sheath formation and loss (3, 9-13). However, how these parameters are balanced to generate this heterogeneity in sheath number has not been thoroughly investigated. To explore this question, we combined extensive time-lapse and longitudinal imaging of oligodendrocytes in the developing zebrafish spinal cord to quantify sheath initiation and loss. Surprisingly, we found that oligodendrocytes repetitively ensheathed the same axons multiple times before any stable sheaths were formed. Importantly, this repetitive ensheathment was independent of neuronal activity. At the level of individual oligodendrocytes, each cell initiated a highly variable number of total ensheathments. However, ~80-90% of these ensheathments always disappeared, an unexpectedly high, but consistent rate of loss. The dynamics of this process indicated rapid membrane turnover as ensheathments were formed and lost repetitively on each axon. To better understand how these sheath initiation dynamics contribute to sheath accumulation and stabilization, we disrupted membrane recycling by expressing a dominant-negative mutant form of Rab5. Oligodendrocytes over-expressing this mutant did not show a change in early sheath initiation dynamics but did lose a higher percentage of ensheathments in the later stabilization phase. Overall, oligodendrocyte sheath number is heterogeneous because each cell repetitively initiates a variable number of total ensheathments that are resolved through a consistent stabilization rate.

摘要

中枢神经系统中的少突胶质细胞支持的髓鞘数量存在显著差异,每个细胞的髓鞘数量从 1 到 50 不等(1-8)。发育过程中的髓鞘生成是动态的,涉及鞘形成和损失(3,9-13)。然而,这些参数如何平衡以产生这种鞘数量的异质性尚未得到彻底研究。为了探讨这个问题,我们结合了对发育中的斑马鱼脊髓中的少突胶质细胞进行的广泛的延时和纵向成像,以定量分析鞘的起始和损失。令人惊讶的是,我们发现少突胶质细胞在形成任何稳定的鞘之前,会多次重复包裹同一个轴突。重要的是,这种重复包裹与神经元活动无关。在单个少突胶质细胞的水平上,每个细胞起始的总包裹数量高度可变。然而,这些包裹中的~80-90%总是消失,这是一个出乎意料的高但一致的损失率。这个过程的动力学表明,随着鞘的形成和重复丢失,膜的周转率很快。为了更好地理解这些鞘起始动力学如何有助于鞘的积累和稳定,我们通过表达 Rab5 的显性负突变体来破坏膜的再循环。过表达这种突变体的少突胶质细胞在早期鞘起始动力学方面没有变化,但在后期稳定阶段失去的包裹比例更高。总体而言,少突胶质细胞的鞘数量是异质的,因为每个细胞都会重复起始可变数量的总包裹,这些包裹通过一致的稳定率得到解决。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/936c26df52d4/elife-82111-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/5d95415544a8/elife-82111-fig1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/3cede69b8014/elife-82111-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/8b3f50ac49ff/elife-82111-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/6466ea6134ad/elife-82111-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/0c75944d6c1b/elife-82111-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/bac1c66f1278/elife-82111-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/029544216617/elife-82111-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/1f80ef82fe2f/elife-82111-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/33220afb3921/elife-82111-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/936c26df52d4/elife-82111-fig6-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/5d95415544a8/elife-82111-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/4bae40bf9a20/elife-82111-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/7cb81e916e8c/elife-82111-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/3cede69b8014/elife-82111-fig3-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/8b3f50ac49ff/elife-82111-fig3-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/6466ea6134ad/elife-82111-fig3-figsupp3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/0c75944d6c1b/elife-82111-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/bac1c66f1278/elife-82111-fig4-figsupp1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/029544216617/elife-82111-fig4-figsupp2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/1f80ef82fe2f/elife-82111-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/33220afb3921/elife-82111-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/963a/10198724/936c26df52d4/elife-82111-fig6-figsupp1.jpg

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本文引用的文献

1
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J Cell Biol. 2023 Mar 6;222(3). doi: 10.1083/jcb.202204010. Epub 2023 Jan 13.
2
Myelination induces axonal hotspots of synaptic vesicle fusion that promote sheath growth.髓鞘化诱导轴突突触囊泡融合的热点,从而促进鞘的生长。
Curr Biol. 2021 Sep 13;31(17):3743-3754.e5. doi: 10.1016/j.cub.2021.06.036. Epub 2021 Jul 15.
3
PAK1 Positively Regulates Oligodendrocyte Morphology and Myelination.PAK1 正向调控少突胶质细胞形态和髓鞘形成。
Biosci Rep. 2024 Sep 25;44(9). doi: 10.1042/BSR20231616.
4
Synaptic vesicle release regulates pre-myelinating oligodendrocyte-axon interactions in a neuron subtype-specific manner.突触小泡释放以神经元亚型特异性方式调节少突胶质前体细胞与轴突之间的相互作用。
Front Cell Neurosci. 2024 May 22;18:1386352. doi: 10.3389/fncel.2024.1386352. eCollection 2024.
5
Dynamics of mature myelin.成熟髓鞘的动力学。
Nat Neurosci. 2024 Aug;27(8):1449-1461. doi: 10.1038/s41593-024-01642-2. Epub 2024 May 21.
6
Small-molecule-induced epigenetic rejuvenation promotes SREBP condensation and overcomes barriers to CNS myelin regeneration.小分子诱导的表观遗传年轻化促进 SREBP 凝聚,克服 CNS 髓鞘再生的障碍。
Cell. 2024 May 9;187(10):2465-2484.e22. doi: 10.1016/j.cell.2024.04.005. Epub 2024 May 2.
7
Identity and Maturity of iPSC-Derived Oligodendrocytes in 2D and Organoid Systems.iPSC 衍生少突胶质细胞在 2D 系统和类器官系统中的鉴定和成熟。
Cells. 2024 Apr 13;13(8):674. doi: 10.3390/cells13080674.
8
Synaptic input and Ca activity in zebrafish oligodendrocyte precursor cells contribute to myelin sheath formation.斑马鱼少突胶质前体细胞中的突触输入和钙活性有助于髓鞘形成。
Nat Neurosci. 2024 Feb;27(2):219-231. doi: 10.1038/s41593-023-01553-8. Epub 2024 Jan 12.
J Neurosci. 2021 Mar 3;41(9):1864-1877. doi: 10.1523/JNEUROSCI.0229-20.2021. Epub 2021 Jan 21.
4
Microglia phagocytose myelin sheaths to modify developmental myelination.小胶质细胞吞噬髓鞘以修饰发育中的髓鞘形成。
Nat Neurosci. 2020 Sep;23(9):1055-1066. doi: 10.1038/s41593-020-0654-2. Epub 2020 Jul 6.
5
Motor learning promotes remyelination via new and surviving oligodendrocytes.运动学习通过新的和存活的少突胶质细胞促进髓鞘再生。
Nat Neurosci. 2020 Jul;23(7):819-831. doi: 10.1038/s41593-020-0637-3. Epub 2020 May 18.
6
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Nat Commun. 2019 Oct 22;10(1):4794. doi: 10.1038/s41467-019-12789-z.
8
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Nat Commun. 2019 Sep 11;10(1):4125. doi: 10.1038/s41467-019-12059-y.
9
Coordinated internodal and paranodal adhesion controls accurate myelination by oligodendrocytes.协调的结间段和结旁黏附控制少突胶质细胞的精确髓鞘形成。
J Cell Biol. 2019 Sep 2;218(9):2887-2895. doi: 10.1083/jcb.201906099. Epub 2019 Aug 26.
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