自闭症谱系障碍
神经发育障碍
自闭症
少突胶质细胞
神经科学
谱系(遗传)
机制(生物学)
发病机制
医学
心理学
免疫学
生物
髓鞘
精神科
中枢神经系统
遗传学
基因
哲学
认识论
出处
期刊:PubMed
日期:2022-09-06
卷期号:56 (9): 1232-1237
标识
DOI:10.3760/cma.j.cn112150-20220529-00541
摘要
Autism spectrum disorder (ASD) is a serious neurodevelopmental impairment of children. Because of its difficulty of early diagnosis, length of disease course, irreversible injury and slim chance of curability, it brings heavy burdens to patients, their families and the whole society. Recent studies have shown that the pathogenic mechanism of ASD is closely related to the abnormal myelination caused by the imbalance of differentiation, proliferation and apoptosis of oligodendroglial lineage cells. This article will review on the role of oligodendroglial lineage cells in myelination and the mechanisms of ASD caused by improper differentiation, proliferation and apoptosis of oligodendroglial lineage cells, according to advanced researches. Oligodendrocytes play vital roles in neurodevelopment, and the defect in these cells has been recognized as one of the key pathogenic mechanisms leading to ASD. Elucidating the effects and disciplines which oligodendrocytes exert on the occurrence and development of ASD would provide guidance for precise prevention and control of neurodevelopmental disorders such as ASD.自闭症谱系障碍(ASD)是一类危害严重的儿童神经发育障碍,具有早期确诊难、病程时间长、损伤不可逆以及难以完全治愈等特点,给患者、家庭和社会带来沉重的负担。近年来的研究表明,ASD的形成机制与少突神经胶质细胞系的分化、增殖及凋亡失调所导致的髓鞘形成异常关联密切。本文将阐述少突神经胶质细胞系细胞在髓鞘形成方面的作用及其分化、增殖、凋亡异常导致ASD发生的机制。少突神经胶质细胞在神经发育中发挥重要作用,其异常是ASD重要致病机制之一。阐明其在ASD发生发展中的作用与机制,对ASD等神经发育疾病精准防控具有积极的指导意义。.
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