神经退行性变
小胶质细胞
生物
特雷姆2
神经科学
机制(生物学)
疾病
中枢神经系统
免疫系统
炎症
免疫学
医学
病理
认识论
哲学
作者
Aleksandra Deczkowska,Hadas Keren‐Shaul,Assaf Weiner,Marco Colonna,Michal Schwartz,Ido Amit
出处
期刊:Cell
[Elsevier]
日期:2018-05-01
卷期号:173 (5): 1073-1081
被引量:898
标识
DOI:10.1016/j.cell.2018.05.003
摘要
A major challenge in the field of neurodegenerative diseases and brain aging is to identify the body's intrinsic mechanism that could sense the central nervous system (CNS) damage early and protect the brain from neurodegeneration. Accumulating evidence suggests that disease-associated microglia (DAM), a recently identified subset of CNS resident macrophages found at sites of neurodegeneration, might play such a protective role. Here, we propose that microglia are endowed with a dedicated sensory mechanism, which includes the Trem2 signaling pathway, to detect damage within the CNS in the form of neurodegeneration-associated molecular patterns (NAMPs). Combining data from transcriptional analysis of DAM at single-cell level and from human genome-wide association studies (GWASs), we discuss potential function of different DAM pathways in the diseased brain and outline how manipulating DAM may create new therapeutic opportunities.
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