Individual neuronal subtypes control initial myelin sheath growth and stabilization.

IF 4 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Heather N Nelson, Anthony J Treichel, Erin N Eggum, Madeline R Martell, Amanda J Kaiser, Allie G Trudel, James R Gronseth, Samantha T Maas, Silas Bergen, Jacob H Hines
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引用次数: 9

Abstract

Background: In the developing central nervous system, pre-myelinating oligodendrocytes sample candidate nerve axons by extending and retracting process extensions. Some contacts stabilize, leading to the initiation of axon wrapping, nascent myelin sheath formation, concentric wrapping and sheath elongation, and sheath stabilization or pruning by oligodendrocytes. Although axonal signals influence the overall process of myelination, the precise oligodendrocyte behaviors that require signaling from axons are not completely understood. In this study, we investigated whether oligodendrocyte behaviors during the early events of myelination are mediated by an oligodendrocyte-intrinsic myelination program or are over-ridden by axonal factors.

Methods: To address this, we utilized in vivo time-lapse imaging in embryonic and larval zebrafish spinal cord during the initial hours and days of axon wrapping and myelination. Transgenic reporter lines marked individual axon subtypes or oligodendrocyte membranes.

Results: In the larval zebrafish spinal cord, individual axon subtypes supported distinct nascent sheath growth rates and stabilization frequencies. Oligodendrocytes ensheathed individual axon subtypes at different rates during a two-day period after initial axon wrapping. When descending reticulospinal axons were ablated, local spinal axons supported a constant ensheathment rate despite the increased ratio of oligodendrocytes to target axons.

Conclusion: We conclude that properties of individual axon subtypes instruct oligodendrocyte behaviors during initial stages of myelination by differentially controlling nascent sheath growth and stabilization.

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单个神经元亚型控制初始髓鞘生长和稳定。
背景:在发育中的中枢神经系统中,髓鞘前少突胶质细胞通过伸展和收缩过程延伸来采集候选神经轴突。一些接触稳定,导致轴突包裹的开始,新生髓鞘形成,同心包裹和鞘伸长,以及少突胶质细胞的鞘稳定或修剪。尽管轴突信号影响髓鞘形成的整个过程,但需要轴突信号的少突胶质细胞的确切行为尚不完全清楚。在这项研究中,我们研究了在髓鞘形成的早期事件中,少突胶质细胞的行为是由少突胶质细胞固有的髓鞘形成程序介导的,还是由轴突因子覆盖的。方法:为了解决这个问题,我们在胚胎和幼体斑马鱼脊髓轴突包裹和髓鞘形成的最初几小时和几天内使用了体内延时成像。转基因报告系标记单个轴突亚型或少突胶质细胞膜。结果:在斑马鱼幼体脊髓中,单个轴突亚型支持不同的新生鞘生长速率和稳定频率。在最初的轴突包裹后的两天内,少突胶质细胞以不同的速率包裹单个轴突亚型。当下行网状脊髓轴突被切除时,尽管少突胶质细胞与目标轴突的比例增加,但局部脊髓轴突支持恒定的鞘鞘率。结论:我们得出结论,在髓鞘形成的初始阶段,单个轴突亚型的特性通过不同地控制新生鞘的生长和稳定来指导少突胶质细胞的行为。
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来源期刊
Neural Development
Neural Development 生物-发育生物学
CiteScore
6.60
自引率
0.00%
发文量
11
审稿时长
>12 weeks
期刊介绍: Neural Development is a peer-reviewed open access, online journal, which features studies that use molecular, cellular, physiological or behavioral methods to provide novel insights into the mechanisms that underlie the formation of the nervous system. Neural Development aims to discover how the nervous system arises and acquires the abilities to sense the world and control adaptive motor output. The field includes analysis of how progenitor cells form a nervous system during embryogenesis, and how the initially formed neural circuits are shaped by experience during early postnatal life. Some studies use well-established, genetically accessible model systems, but valuable insights are also obtained from less traditional models that provide behavioral or evolutionary insights.
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