衰老过程中人脑区域和细胞类型的特异性变化

Human Brain Pub Date : 2024-01-10 DOI:10.37819/hb.3.1780
Yanxi Chen, Gaoyu Zu, Bill Ling Feng Zhang, Zhixin Bai, Qiong Liu, Wensheng Li, Linya You
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引用次数: 0

摘要

随着年龄的增长,认知能力的衰退变得越来越明显,同时也更容易患上神经退行性疾病和痴呆症。此外,慢性神经精神疾病的症状也会随着年龄的增长而加重。必须强调的是,衰老过程对个体的影响并不一致,即使是对同一个人,其影响也会有所不同。本综述旨在总结健康老龄化对人脑的影响,重点关注不同脑区和细胞类型的变化。根据具体脑区的不同,大脑在衰老过程中会出现变薄、体积缩小、区域萎缩、组织完整性破坏、细胞复杂性降低或铁积累等现象。此外,在衰老过程中,脑细胞的形态和功能也会发生变化。神经元发生变化的特点是树突、树突棘和轴突减少,髓鞘更不紧密,从而导致突触大量丧失。相对而言,神经胶质细胞通常会转变为反应性表型。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regional- and cell type-specific changes of the human brain during aging
As individuals age, cognitive decline becomes more prominent, concomitant with an elevated susceptibility to neurodegenerative diseases and dementia. Additionally, symptoms of chronic neuropsychiatric diseases tend to worsen with age. It is crucial to highlight that the aging process does not affect individuals uniformly, and its effects can vary, even within the same person. This review aims to summary the impact of healthy aging on the human brain, focusing on the variations from different brain regions and cell types. Depending on specific brain regions, the brain exhibits thinning, volume reduction, regional shrinkage, disrupted tissue integrity, decreased cell complexity, or iron accumulation during aging. Moreover, the brain cells exhibit morphology and function changes during aging. Neurons undergo changes characterized by reduced dendrites, dendritic spines, and axons with less compact myelin sheaths, leading to a significant loss of synapses. Comparatively, glia often transform into a reactive phenotype.
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