Oligodendroglia in Ageing and Age-Dependent Neurodegenerative Diseases.

Q3 Neuroscience
Jianqin Niu, Alexei Verkhratsky, Arthur Butt, Chenju Yi
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引用次数: 0

Abstract

The central nervous system is susceptible to gradual decline with age, affecting all types of glial cells in the process. Compared to other glial cells, the oligodendroglial lineage is highly vulnerable to ageing and undergoes significant characteristic changes that impact upon its structure and impair its physiological functions. Therefore, the ageing and degeneration of oligodendroglia become major risk factors for neurodegenerative diseases. During the age-related disease process, changes in oligodendroglia lead to a decline in their ability to regenerate myelin and respond to the aged microenvironment, which are closely linked to the pathogenesis of neurodegenerative diseases, facilitating the emergence of these diseases in older populations. In this chapter, we introduce the physiological changes of oligodendroglia during ageing and the related mechanisms and then summarise their pathophysiological contributions to age-related cognitive disorders. Finally, we discuss potential therapeutic strategies that target oligodendroglia for future research on neurodegenerative diseases.

衰老和年龄依赖性神经退行性疾病中的少突胶质细胞。
随着年龄的增长,中枢神经系统容易逐渐衰退,在这个过程中影响到所有类型的胶质细胞。与其他神经胶质细胞相比,少突胶质细胞谱系极易受到衰老的影响,并经历显著的特征变化,影响其结构和损害其生理功能。因此,少突胶质细胞的老化和变性成为神经退行性疾病的主要危险因素。在与年龄相关的疾病过程中,少突胶质细胞的变化导致其再生髓磷脂和对衰老微环境的反应能力下降,这与神经退行性疾病的发病机制密切相关,促进了老年人群中这些疾病的出现。在这一章中,我们介绍了少突胶质细胞在衰老过程中的生理变化及其相关机制,并总结了它们在衰老相关认知障碍中的病理生理作用。最后,我们讨论了针对少突胶质细胞的潜在治疗策略,用于未来神经退行性疾病的研究。
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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