Complex formation of APP with GABAB receptors links axonal trafficking to amyloidogenic processing.

ABSTRACT: GABAB receptors (GBRs) are key regulators of synaptic release but little is known about trafficking mechanisms that control their presynaptic abundance. We now show that sequence-related epitopes in APP, AJAP-1 and PIANP bind with nanomolar affinities to the N-terminal sushi-domain of presynaptic GBRs. Of the three interacting proteins, selectively the genetic loss of APP impaired GBR-mediated presynaptic inhibition and axonal GBR expression. Proteomic and functional analyses revealed that APP associates with JIP and calsyntenin proteins that link the APP/GBR complex in cargo vesicles to the axonal trafficking motor. Complex formation with GBRs stabilizes APP at the cell surface and reduces proteolysis of APP to A?, a component of senile plaques in Alzheimer's disease patients. Thus, APP/GBR complex formation links presynaptic GBR trafficking to A? formation. Our findings support that dysfunctional axonal trafficking and reduced GBR expression in Alzheimer's disease increases A? formation.

SUBMITTER: Dinamarca MC 

PROVIDER: S-EPMC6430795 | biostudies-literature | 2019 Mar

REPOSITORIES: biostudies-literature