| First Author | He A | Year | 2026 |
| Journal | Nat Aging | Volume | 6 |
| Issue | 1 | Pages | 181-199 |
| PubMed ID | 41419665 | Mgi Jnum | J:386200 |
| Mgi Id | MGI:8331832 | Doi | 10.1038/s43587-025-01028-4 |
| Citation | He A, et al. (2026) Allosteric activation of a cell-type-specific GPR120 inhibits amyloid pathology of Alzheimer's disease. Nat Aging 6(1):181-199 |
| abstractText | Black rice diets are enriched with unsaturated fatty acids that are thought to be beneficial for neurodegenerative disorders in aging. Here we find that alpha-linolenic acid (ALA) and 11,14-eicosadienoic acid (EDA), which are naturally enriched in black rice, inhibit amyloid pathology, rescue cognition and extend lifespan in mouse preclinical models of Alzheimer's disease via allosteric activation of G protein-coupled receptor 120 (GPR120) in plaque-associated macrophages and activated microglia. We generate the structures of GPR120 bound to ALA and EDA. We demonstrate that ALA and EDA allosterically modulate and synergistically activate GPR120 for macrophagic phagocytosis and clearance of beta-amyloid aggregates in Alzheimer's disease mice. A cell-type-specific deletion of GPR120, or Galphai1, completely abrogates the therapeutic effects of ALA and EDA. This deletion can be rescued by a constitutive active Galphai1-Q204L. These findings show a cell-type-specific function of GPR120 in the brain and provide an enriched allosteric mechanism of GPR120 activation for the treatment of Alzheimer's disease. |
