Seeing Is Believing: Insights into Myelination and Remyelination in Zebrafish.

Q3 Neuroscience
Peng Liu, Qiang Chen, Cheng He
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Abstract

Myelin is the lipid-rich insulating layer that wraps axons, providing trophic support and ensuring rapid propagation of the electrical impulses that underlie nervous system function. In the CNS, myelin is produced by mature oligodendrocytes (OLs) that arise from oligodendrocyte precursor cells (OPCs). Myelination is regulated by a variety of molecules, including growth factors, hormones, and extracellular molecules, which activate signaling cascades that drive cellular maturation. Key signaling molecules and downstream pathways that control myelination have been identified in cell culture and rodent models. Although much is known about the development of OL and its progenitor cell in vitro and in vivo, how CNS myelin is dynamically formed through OL processes is still unclear. Zebrafish share significant genetic and physiological similarities with mammals, including humans, making them a relevant model for studying complex biological processes like myelination. Due to its transparent larval development, zebrafish facilitates live imaging studies, enabling dynamic visualizations of cellular and molecular processes in real-time studies. In this chapter, we reviewed the latest insights into OL development and myelin formation, with a particular emphasis on the mechanisms regulating dynamic myelination in zebrafish. We highlight the dynamic extension and retraction of myelin sheath segments and the role of neuronal activity in regulating the developmental myelination in zebrafish. In addition, we also discussed the mechanisms of Ranvier node positioning and axon targeting of myelin sheaths in the spinal cord of zebrafish larvae. Finally, we reviewed the recent progress of zebrafish as a demyelinating disease model for drug discovery of pharmacological compounds favoring myelin regeneration.

眼见为实:洞察斑马鱼的髓鞘形成和再髓鞘形成。
髓磷脂是包裹轴突的富含脂质的绝缘层,提供营养支持并确保神经系统功能基础上的电脉冲的快速传播。在中枢神经系统中,髓磷脂是由成熟的少突胶质细胞(OLs)产生的,它起源于少突胶质前体细胞(OPCs)。髓鞘形成受多种分子调控,包括生长因子、激素和细胞外分子,这些分子激活了驱动细胞成熟的信号级联反应。关键的信号分子和下游途径控制髓鞘形成已经确定在细胞培养和啮齿动物模型。尽管我们对OL及其祖细胞在体外和体内的发育了解甚多,但中枢神经系统髓磷脂是如何通过OL过程动态形成的仍不清楚。斑马鱼与包括人类在内的哺乳动物有着显著的遗传和生理相似性,这使它们成为研究髓鞘形成等复杂生物过程的相关模型。由于其透明的幼虫发育,斑马鱼促进了实时成像研究,使实时研究中的细胞和分子过程的动态可视化成为可能。在本章中,我们回顾了OL发育和髓鞘形成的最新见解,特别强调了斑马鱼动态髓鞘形成的调节机制。我们强调髓鞘节段的动态延伸和收缩以及神经元活动在调节斑马鱼髓鞘形成发育中的作用。此外,我们还讨论了斑马鱼幼体脊髓髓鞘的Ranvier节点定位和轴突靶向机制。最后,我们回顾了斑马鱼作为脱髓鞘疾病模型的最新进展,以发现有利于髓鞘再生的药理化合物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
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0.00%
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