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神经胶质细胞促进髓鞘形成与清除。

Glial Cells Promote Myelin Formation and Elimination.

作者信息

Hughes Alexandria N

机构信息

Section of Developmental Biology, Department of Pediatrics, University of Colorado, Aurora, Aurora, CO, United States.

出版信息

Front Cell Dev Biol. 2021 May 11;9:661486. doi: 10.3389/fcell.2021.661486. eCollection 2021.

Abstract

Building a functional nervous system requires the coordinated actions of many glial cells. In the vertebrate central nervous system (CNS), oligodendrocytes myelinate neuronal axons to increase conduction velocity and provide trophic support. Myelination can be modified by local signaling at the axon-myelin interface, potentially adapting sheaths to support the metabolic needs and physiology of individual neurons. However, neurons and oligodendrocytes are not wholly responsible for crafting the myelination patterns seen . Other cell types of the CNS, including microglia and astrocytes, modify myelination. In this review, I cover the contributions of non-neuronal, non-oligodendroglial cells to the formation, maintenance, and pruning of myelin sheaths. I address ways that these cell types interact with the oligodendrocyte lineage throughout development to modify myelination. Additionally, I discuss mechanisms by which these cells may indirectly tune myelination by regulating neuronal activity. Understanding how glial-glial interactions regulate myelination is essential for understanding how the brain functions as a whole and for developing strategies to repair myelin in disease.

摘要

构建一个功能正常的神经系统需要许多神经胶质细胞的协同作用。在脊椎动物的中枢神经系统(CNS)中,少突胶质细胞使神经元轴突形成髓鞘,以提高传导速度并提供营养支持。髓鞘形成可通过轴突-髓鞘界面处的局部信号传导进行调节,这可能使髓鞘适应单个神经元的代谢需求和生理功能。然而,神经元和少突胶质细胞并非完全负责形成所观察到的髓鞘形成模式。中枢神经系统的其他细胞类型,包括小胶质细胞和星形胶质细胞,也会对髓鞘形成产生影响。在这篇综述中,我将阐述非神经元、非少突胶质细胞对髓鞘形成、维持和修剪的贡献。我将探讨这些细胞类型在整个发育过程中与少突胶质细胞谱系相互作用以改变髓鞘形成的方式。此外,我还将讨论这些细胞可能通过调节神经元活动间接调节髓鞘形成的机制。了解神经胶质细胞间的相互作用如何调节髓鞘形成对于理解大脑的整体功能以及制定疾病中修复髓鞘的策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c5b/8144722/340706e634f7/fcell-09-661486-g001.jpg

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