轴突的鞘鞘和髓鞘形成:神经胶质功能的进化。

IF 12.1 1区 医学 Q1 NEUROSCIENCES
Annual review of neuroscience Pub Date : 2021-07-08 Epub Date: 2021-03-15 DOI:10.1146/annurev-neuro-100120-122621
Klaus-Armin Nave, Hauke B Werner
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引用次数: 39

摘要

轴突的髓鞘形成为沿脊椎动物纤维束的快速跳跃脉冲传播提供了结构基础,这是一个公认的神经生理学概念。然而,髓鞘少突胶质细胞和雪旺细胞在神经元能量代谢中具有额外的功能,这些功能与无髓鞘无脊椎动物的轴突鞘胶质细胞非常相似。在这里,我们讨论髓磷脂进化和生理胶质功能,从鞘鞘胶质在防止突触偶联、轴胶质代谢支持和消除氧化自由基中的作用开始。在脊椎动物和无脊椎动物中,轴胶质相互作用是双向的,用于调节细胞命运、神经传导和行为表现。在脊椎动物谱系中致密髓磷脂进化的一个关键步骤是在另一个基因中出现髓磷脂碱性蛋白的开放阅读框。其他几种蛋白质被新功能化为髓磷脂成分,并帮助维持健康的神经系统。脊椎动物的髓鞘形成成为居住在新生态位的主要先决条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ensheathment and Myelination of Axons: Evolution of Glial Functions.

Myelination of axons provides the structural basis for rapid saltatory impulse propagation along vertebrate fiber tracts, a well-established neurophysiological concept. However, myelinating oligodendrocytes and Schwann cells serve additional functions in neuronal energy metabolism that are remarkably similar to those of axon-ensheathing glial cells in unmyelinated invertebrates. Here we discuss myelin evolution and physiological glial functions, beginning with the role of ensheathing glia in preventing ephaptic coupling, axoglial metabolic support, and eliminating oxidative radicals. In both vertebrates and invertebrates, axoglial interactions are bidirectional, serving to regulate cell fate, nerve conduction, and behavioral performance. One key step in the evolution of compact myelin in the vertebrate lineage was the emergence of the open reading frame for myelin basic protein within another gene. Several other proteins were neofunctionalized as myelin constituents and help maintain a healthy nervous system. Myelination in vertebrates became a major prerequisite of inhabiting new ecological niches.

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来源期刊
Annual review of neuroscience
Annual review of neuroscience 医学-神经科学
CiteScore
25.30
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Neuroscience is a well-established and comprehensive journal in the field of neuroscience, with a rich history and a commitment to open access and scholarly communication. The journal has been in publication since 1978, providing a long-standing source of authoritative reviews in neuroscience. The Annual Review of Neuroscience encompasses a wide range of topics within neuroscience, including but not limited to: Molecular and cellular neuroscience, Neurogenetics, Developmental neuroscience, Neural plasticity and repair, Systems neuroscience, Cognitive neuroscience, Behavioral neuroscience, Neurobiology of disease. Occasionally, the journal also features reviews on the history of neuroscience and ethical considerations within the field.
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