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首页|期刊导航|基础医学与临床|单细胞图谱揭示阿尔茨海默病模型小鼠小胶质细胞对衰老程序的病理性放大及蛋白质稳态崩溃

单细胞图谱揭示阿尔茨海默病模型小鼠小胶质细胞对衰老程序的病理性放大及蛋白质稳态崩溃

周子群 李炳男

基础医学与临床2026,Vol.46Issue(6):791-799,9.
基础医学与临床2026,Vol.46Issue(6):791-799,9.DOI:10.16352/j.issn.1001-6325.2026.06.0791

单细胞图谱揭示阿尔茨海默病模型小鼠小胶质细胞对衰老程序的病理性放大及蛋白质稳态崩溃

Single-cell atlas reveals pathological amplification of aging programs and proteostasis collapse in microglia of Alzheimer's disease mice

周子群 1李炳男1

作者信息

  • 1. 中国医学科学院北京协和医学院 基础医学研究所 重大疾病共性机制研究全国重点实验室,北京 100005
  • 折叠

摘要

Abstract

Objective To explore the intrinsic relationship between microglia in Alzheimer's disease(AD)and natural aging,and their role in mediating microenvironmental proteostasis.Methods Nearly 1.69 million brain single-cell and single-nucleus transcriptomes from 18 public datasets were integrated and annotated using deep gen-erative models.A"transcriptomic aging score"was constructed to compare the transcriptional remodeling of micro-glia between natural aging and AD models.Multiplex immunofluorescence staining on brain sections was performed to verify the in situ expression of key molecules for proteostasis and lysosomes.A Trem2-deficient model was intro-duced to explore the regulatory mechanisms.Results AD pathology significantly accelerated the age-dependent accumulation of late-stage disease-associated microglia(DAM-Late).The AD transcriptional profile showed a highly significant positive correlation with natural aging(R=0.481),manifesting as a"pathological amplification"of aging-mediated lipid metabolism and lysosomal programs.Metabolic stress led to the collapse of microglial pro-teostasis,with a significant increase in the area and number of αB-CRYSTALLIN,CD68,and UBC puncta carried by single cells in the hypothalamus of AD mice.TREM2 acted as a key switch initiating the compensatory program,and its deficiency led to phenotypic decoupling and functional compensation failure.Conclusions The pathological activation of AD microglia significantly amplifies endogenous aging characteristics.Under continuous pathological stress,this adaptive compensation may ultimately mediate severe impairment of proteostasis in the microenvironment and adjacent cells.

关键词

阿尔茨海默病/小胶质细胞/衰老/单细胞转录组测序

Key words

Alzheimer's disease/microglia/aging/single-cell transcriptomic sequencing

分类

医药卫生

引用本文复制引用

周子群,李炳男..单细胞图谱揭示阿尔茨海默病模型小鼠小胶质细胞对衰老程序的病理性放大及蛋白质稳态崩溃[J].基础医学与临床,2026,46(6):791-799,9.

基金项目

国家自然科学基金重大项目(32293213) (32293213)

北京协和医学院高层次人才培养项目(3332024218) (3332024218)

基础医学与临床

1001-6325

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