Physiology of oligodendroglia.

IF 28.7 1区 医学 Q1 PHYSIOLOGY
Physiological reviews Pub Date : 2026-07-01 Epub Date: 2026-03-06 DOI:10.1152/physrev.00023.2025
Arthur M Butt, Jianqin Niu, Chenju Yi, Alexei Verkhratsky
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引用次数: 0

Abstract

Oligodendrocytes are highly specialized neural cells that produce myelin, essential for rapid electrical conduction of neural signals in the central nervous system (CNS). The emergence of oligodendrocytes and myelin was a critical step in the evolution of vertebrates, fundamental for the development of the mammalian connectome, and indispensable for miniaturization and enhanced computing power of the brain. The advance in cognitive capacity is paralleled by increasing eminence of white matter, composed of interconnected bundles of myelinated axons; white matter volume increases from 6% of the brain in shrews, considered related to the most primitive mammals, up to 50% in Homo sapiens. Myelinating oligodendrocytes together with smaller populations of oligodendrocyte precursor cells (OPCs) and satellite or perineuronal oligodendrocytes account for more than half of the glial cells in the human brain. Together, these three cell types make up the oligodendroglial cell lineage that express common lineage-specific proteins and transcription factors and display a degree of molecular and functional diversity. OPCs are the most numerous oligodendroglial cells during developmental axonal myelination, which extends postnatally for many years in humans. The generation of myelinating oligodendrocytes from OPCs throughout life continues to be important for adaptive plasticity of neural circuits and myelination of new axons required for learning. Myelination decreases in the aging brain and correlates with natural or physiological age-related cognitive decline. Like all neural cells, oligodendroglia express a wide assortment of ion channels, transporters, and neurotransmitter receptors that are essential for maintaining neuronal signaling, principally myelination, axonal metabolic support, and homeostatic regulation of the periaxonal microenvironment. Notably, OPCs are unique among neuroglia in that, like neurons, they are electrically excitable and form synapses with neurons. Oligodendroglial cells also contribute to neuroplasticity through multiple mechanisms including axon guidance, synapse formation, and adaptive myelination. In short, oligodendroglia are essential for normal CNS integrity, cognitive function, and behavior.

少突胶质细胞生理学。
少突胶质细胞是高度特化的神经细胞,可产生髓磷脂,髓磷脂对中枢神经系统(CNS)神经信号的快速电传导至关重要。少突胶质细胞和髓磷脂的出现是脊椎动物进化的关键一步,也是哺乳动物连接体发育的基础,对大脑的小型化和增强计算能力必不可少。认知能力的提高与白质的增加是平行的,白质是由相互连接的髓鞘轴突束组成的;大脑白质的体积从鼩鼱的6%(被认为与最原始的哺乳动物有关)增加到智人的50%。髓鞘性少突胶质细胞与较少的少突胶质前体细胞(OPCs)和卫星细胞或神经元周围少突胶质细胞一起占人脑胶质细胞的一半以上。总之,这三种细胞类型构成了少突胶质细胞谱系,表达共同谱系特异性蛋白质和转录因子,并显示一定程度的分子和功能多样性。OPCs是发育性轴突髓鞘形成过程中数量最多的少突胶质细胞,其在人类出生后可延续多年。在整个生命过程中,OPCs的髓鞘化少突胶质细胞的产生对于神经回路的适应性可塑性和学习所需的新轴突的髓鞘化仍然是重要的。髓鞘形成在衰老的大脑中减少,与自然或生理年龄相关的认知能力下降有关。像所有的神经细胞一样,少突胶质细胞表达各种各样的离子通道、转运体和神经递质受体,这些对于维持神经元信号传导至关重要,主要是髓鞘形成、轴突代谢支持和轴突周围微环境的稳态调节。值得注意的是,OPCs在神经胶质中是独一无二的,就像神经元一样,它们是可电兴奋的,并与神经元形成突触。少突胶质细胞还通过多种机制促进神经可塑性,包括轴突引导、突触形成和适应性髓鞘形成。简而言之,少突胶质细胞对正常的中枢神经系统完整性、认知功能和行为至关重要。
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
Physiological reviews
Physiological reviews 医学-生理学
CiteScore
56.50
自引率
0.90%
发文量
53
期刊介绍: Physiological Reviews is a highly regarded journal that covers timely issues in physiological and biomedical sciences. It is targeted towards physiologists, neuroscientists, cell biologists, biophysicists, and clinicians with a special interest in pathophysiology. The journal has an ISSN of 0031-9333 for print and 1522-1210 for online versions. It has a unique publishing frequency where articles are published individually, but regular quarterly issues are also released in January, April, July, and October. The articles in this journal provide state-of-the-art and comprehensive coverage of various topics. They are valuable for teaching and research purposes as they offer interesting and clearly written updates on important new developments. Physiological Reviews holds a prominent position in the scientific community and consistently ranks as the most impactful journal in the field of physiology.
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