Genetic studies have highlighted microglia as pivotal in orchestrating Alzheimer's disease (AD). Microglia that adhere to Aβ plaques acquire a transcriptional signature, "disease-associated microglia" (DAM), which largely emanates from the TREM2-DAP12 receptor complex that transmits intracellular signals through the protein tyrosine kinase SYK. The human TREM2R47H variant associated with high AD risk fails to activate microglia via SYK. We found that SYK-deficient microglia cannot encase Aβ plaques, accelerating brain pathology and behavioral deficits. SYK deficiency impaired the PI3K-AKT-GSK-3β-mTOR pathway, incapacitating anabolic support required for attaining the DAM profile. However, SYK-deficient microglia proliferated and advanced to an Apoe-expressing prodromal stage of DAM; this pathway relied on the adapter DAP10, which also binds TREM2. Thus, microglial responses to Aβ involve non-redundant SYK- and DAP10-pathways. Systemic administration of an antibody against CLEC7A, a receptor that directly activates SYK, rescued microglia activation in mice expressing the TREM2R47H allele, unveiling new options for AD immunotherapy.

TREM2 drives microglia response to amyloid-β via SYK-dependent and -independent pathways / Wang, Shoutang; Sudan, Raki; Peng, Vincent; Zhou, Yingyue; Du, Siling; Yuede, Carla M; Lei, Tingting; Hou, Jinchao; Cai, Zhangying; Cella, Marina; Nguyen, Khai; Poliani, Pietro L; Beatty, Wandy L; Chen, Yun; Cao, Siyan; Lin, Kent; Rodrigues, Cecilia; Ellebedy, Ali H; Gilfillan, Susan; Brown, Gordon D; Holtzman, David M; Brioschi, Simone; Colonna, Marco. - In: CELL. - ISSN 1097-4172. - 185:22(2022), pp. 4153-4169. [10.1016/j.cell.2022.09.033]

TREM2 drives microglia response to amyloid-β via SYK-dependent and -independent pathways

Poliani, Pietro L;
2022-01-01

Abstract

Genetic studies have highlighted microglia as pivotal in orchestrating Alzheimer's disease (AD). Microglia that adhere to Aβ plaques acquire a transcriptional signature, "disease-associated microglia" (DAM), which largely emanates from the TREM2-DAP12 receptor complex that transmits intracellular signals through the protein tyrosine kinase SYK. The human TREM2R47H variant associated with high AD risk fails to activate microglia via SYK. We found that SYK-deficient microglia cannot encase Aβ plaques, accelerating brain pathology and behavioral deficits. SYK deficiency impaired the PI3K-AKT-GSK-3β-mTOR pathway, incapacitating anabolic support required for attaining the DAM profile. However, SYK-deficient microglia proliferated and advanced to an Apoe-expressing prodromal stage of DAM; this pathway relied on the adapter DAP10, which also binds TREM2. Thus, microglial responses to Aβ involve non-redundant SYK- and DAP10-pathways. Systemic administration of an antibody against CLEC7A, a receptor that directly activates SYK, rescued microglia activation in mice expressing the TREM2R47H allele, unveiling new options for AD immunotherapy.
2022
Alzheimer's disease
ApoE
Syk
TREM2
immunotherapy
metabolism
microglia
signaling
Animals
Mice
Humans
Glycogen Synthase Kinase 3 beta
Phosphatidylinositol 3-Kinases
Amyloid beta-Peptides
Plaque
Amyloid
Disease Models
Animal
Syk Kinase
Microglia
Alzheimer Disease
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.11768/146117
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