代谢组学
代谢物
转录组
老化
新陈代谢
细胞生物学
化学
谷胱甘肽
生物化学
小胶质细胞
体内
代谢途径
生物
神经退行性变
细胞
下调和上调
星形胶质细胞
电池类型
多胺
神经毒素
细胞外
神经科学
代谢组
细胞生长
神经胶质
神经元
脑化学
中枢神经系统
基因表达谱
基因
生物途径
基因表达
细胞培养
神经黑素
亚精胺
作者
J K Yu,Fengzhi Li,Xing-jun Chen,Chenye Mou,Di Yao,Zhanying Bi,X G Chen,Lulu Du,Ziyan Feng,Xi Zhang,Xiaoqian Yu,Lauren G. Zacharias,Ralph J DeBerardinis,Li Zhang,Zhen Li,Benyan Luo,Xiao-Ling Hu,Woo-Ping Ge
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-04-30
标识
DOI:10.1038/s41556-026-01910-2
摘要
Neurons and glia are distinct in their morphology, development and function, possessing unique transcriptomes and proteomes, but little is known about their metabolomes. The challenge of brain cell metabolic profiling is to obtain a large number of cells for reliable analysis. Here we purified microglia, astrocytes and neurons from mouse brains, identifying >70 metabolites through targeted metabolomics and 9,854 metabolite features via untargeted metabolomics. We systematically characterized cell type-enriched metabolites and metabolic pathways, revealing an enrichment of glutathione (GSH) and polyamine metabolism in microglia. This enrichment was validated in vivo and showed significant decreases with ageing and in an Alzheimer's disease model. Notably, GSH and polyamine metabolism correlated strongly with chemokine-related gene expression. Disrupting the GSH pathway in microglia resulted in downregulation of chemokine-related genes, aberrant morphogenesis and β-amyloid deposition. Our results provide a valuable resource ( https://metabolismocean.org/braincell ) for metabolic studies related to ageing, Alzheimer's disease and other neurological diseases.
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