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Abstract
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.