Early disruption of entorhinal dopamine in a knock-in model of Alzheimer's disease

• Published in: bioRxiv
• Main Authors: Nakagawa, Tatsuki, Xie, Jiayun L, Savadkohighodjanaki, Marjan, Zhang, Yutian J, Jun, Heechul, Cao, Kai, Ichii, Ayana, Lee, Jason Y, Soma, Shogo, Medhat, Yasmeen K, Saido, Takaomi C, Igarashi, Kei M
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory 12.10.2024
• ISSN: 2692-8205; 2692-8205
• DOI: 10.1101/2024.10.10.617678

The entorhinal cortex (EC) is a critical brain area for memory formation, while also the region exhibiting the earliest histological and functional alterations in Alzheimer's disease (AD). The EC thus has been long hypothesized as one of the originating brain areas of AD pathophysiology, although circuit mechanisms causing its selective vulnerability remain poorly understood. We found that dopamine neurons projecting their axons to the lateral EC (LEC), critical for memory formation in healthy brains, become dysfunctional and cause memory impairments in early AD brains. In amyloid precursor protein knock-in mice with associative memory impairment, LEC dopamine activity and associative memory encoding of LEC layer 2/3 neurons were disrupted in parallel from the early pathological stage. Optogenetic reactivation of LEC dopamine fibers, as well as L- DOPA treatment, rescued associative learning behavior. These results suggest that dysfunction of LEC-projecting dopamine neurons underlies memory impairment in AD from early stages, pointing to a need for clinical investigation of LEC dopamine in AD patients.