| Literature DB >> 36199750 |
Alberto Serrano-Pozo1,2,3, Zhaozhi Li1,2, Ayush Noori1,2, Huong N Nguyen1, Aziz Mezlini1,2,3, Liang Li1, Eloise Hudry1,3, Rosemary J Jackson1,3, Bradley T Hyman1,2,3, Sudeshna Das1,2,3.
Abstract
The roles of APOEε4 and APOEε2-the strongest genetic risk and protective factors for Alzheimer's disease-in glial responses remain elusive. We tested the hypothesis that APOE alleles differentially impact glial responses by investigating their effects on the glial transcriptome from elderly control brains with no neuritic amyloid plaques. We identified a cluster of microglial genes that are upregulated in APOEε4 and downregulated in APOEε2 carriers relative to APOEε3 homozygotes. This microglia-APOE cluster is enriched in phagocytosis-including TREM2 and TYROBP-and proinflammatory genes, and is also detectable in brains with frequent neuritic plaques. Next, we tested these findings in APOE knock-in mice exposed to acute (lipopolysaccharide challenge) and chronic (cerebral β-amyloidosis) insults and found that these mice partially recapitulate human APOE-linked expression patterns. Thus, the APOEε4 allele might prime microglia towards a phagocytic and proinflammatory state through an APOE-TREM2-TYROBP axis in normal aging as well as in Alzheimer's disease.Entities:
Year: 2021 PMID： 36199750 PMCID： PMC9531903 DOI： 10.1038/s43587-021-00123-6
Source DB: PubMed Journal: Nat Aging ISSN： 2662-8465