重编程
小胶质细胞
免疫系统
神经科学
疾病
生物
功能(生物学)
免疫学
炎症
认知功能衰退
碳水化合物代谢
中枢神经系统
表型
神经保护
免疫疗法
代谢控制分析
细胞代谢
生物信息学
神经炎症
神经免疫学
细胞代谢
医学
干预(咨询)
糖尿病
神经退行性变
认知
作者
Qingyu Cao,Mengmeng Shen,Yan Liu,Caicai Li,Lu Liu,Jidong Zhou,Rujing Yue,Dejun Niu,Yayun Ren,Lihong Pan,Jingchun Yao,Guimin Zhang
标识
DOI:10.1177/13872877261478594
摘要
Alzheimer's disease (AD) is a neurodegenerative disorder characterized by progressive cognitive impairment, and there remains a lack of effective treatments capable of reversing or significantly slowing disease progression. Accumulating evidence indicates that the immune function of microglia, the resident immune cells of the central nervous system, is a critical factor in regulating AD pathogenesis. Emerging research in immunometabolism further reveals that glucose metabolic reprogramming serves as a central driver of microglial phenotypic and functional differentiation. This review systematically outlines the fundamental characteristics of microglial glucose metabolism and focuses on how the dynamic metabolic reprogramming it undergoes during AD progression regulates microglial immune behavior and inflammatory responses. Building on this, we further summarize key regulatory targets within the "metabolism-immune axis" and corresponding pharmacological intervention strategies. Finally, this article discusses current challenges and future research directions in the field of microglial immunometabolism. This review aims to provide a theoretical foundation for AD intervention strategies targeting the "metabolism-immune axis" and to offer insights for the development of novel disease-modifying therapeutics.
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