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少突胶质细胞谱系细胞在阿尔茨海默病发病机制中的作用

The Role of Oligodendrocyte Lineage Cells in the Pathogenesis of Alzheimer's Disease.

作者信息

Liu Xiaodong, Lv Zhengxiang, Huang Qin, Lei Yihui, Liu Haijun, Xu Ping

机构信息

Department of Neurology, Affiliated Hospital of Zunyi Medical University, Zunyi, China.

Department of Neurology, China Guihang Group 302 Hospital, Anshun, China.

出版信息

Neurochem Res. 2025 Jan 3;50(1):72. doi: 10.1007/s11064-024-04325-3.

Abstract

Alzheimer's disease (AD) is a central nervous system degenerative disease with a stealthy onset and a progressive course characterized by memory loss, cognitive dysfunction, and abnormal psychological and behavioral symptoms. However, the pathogenesis of AD remains elusive. An increasing number of studies have shown that oligodendrocyte progenitor cells (OPCs) and oligodendroglial lineage cells (OLGs), especially OPCs and mature oligodendrocytes (OLGs), which are derived from OPCs, play important roles in the pathogenesis of AD. OLGs function mainly by myelinating axons, transmitting electrical signals, and regulating neural development. In addition to myelin, OPCs and OLGs can also participate in AD pathogenesis in other ways. This review summarizes the mechanisms by which OPCs and OLGs affect myelin formation, oxidative stress, neuroinflammation, the blood-brain barrier, synaptic function, and amyloid-beta protein and further elucidates the mechanisms by which oligodendrocyte lineage cells participate in AD pathogenesis and treatment, which is highly important for clarifying the pathogenesis of AD, clinical treatment, and prevention.

摘要

阿尔茨海默病(AD)是一种中枢神经系统退行性疾病,起病隐匿,病程呈进行性,以记忆力减退、认知功能障碍以及异常的心理和行为症状为特征。然而,AD的发病机制仍不清楚。越来越多的研究表明,少突胶质前体细胞(OPCs)和少突胶质谱系细胞(OLGs),尤其是OPCs以及由OPCs分化而来的成熟少突胶质细胞(OLGs),在AD的发病机制中发挥着重要作用。OLGs主要通过对轴突进行髓鞘化、传递电信号以及调节神经发育来发挥功能。除了髓鞘形成,OPCs和OLGs还能以其他方式参与AD的发病过程。本综述总结了OPCs和OLGs影响髓鞘形成、氧化应激、神经炎症、血脑屏障、突触功能以及β-淀粉样蛋白的机制,并进一步阐明了少突胶质谱系细胞参与AD发病机制及治疗的机制,这对于阐明AD的发病机制、临床治疗及预防具有重要意义。

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