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Dunot, J.* ; Moreno, S.G.* ; Gandin, C.* ; Pousinha, P.A.* ; Amici, M.* ; Dupuis, J.* ; Anisimova, M.* ; Winschel, A.* ; Uriot, M.* ; Petshow, S.J.* ; Mensch, M.* ; Bethus, I.* ; Giudici, C.* ; Hampel, H.* ; Wefers, B. ; Wurst, W. ; Naumann, R.* ; Ashby, M.C.* ; Laube, B.* ; Zito, K.* ; Mellor, J.R.* ; Groc, L.* ; Willem, M.* ; Marie, H.*

APP fragment controls both ionotropic and non-ionotropic signaling of NMDA receptors.

Neuron 112, 2708-2720.e9 (2024)
Verlagsversion DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
NMDA receptors (NMDARs) are ionotropic receptors crucial for brain information processing. Yet, evidence also supports an ion-flux-independent signaling mode mediating synaptic long-term depression (LTD) and spine shrinkage. Here, we identify AETA (Aη), an amyloid-β precursor protein (APP) cleavage product, as an NMDAR modulator with the unique dual regulatory capacity to impact both signaling modes. AETA inhibits ionotropic NMDAR activity by competing with the co-agonist and induces an intracellular conformational modification of GluN1 subunits. This favors non-ionotropic NMDAR signaling leading to enhanced LTD and favors spine shrinkage. Endogenously, AETA production is increased by in vivo chemogenetically induced neuronal activity. Genetic deletion of AETA production alters NMDAR transmission and prevents LTD, phenotypes rescued by acute exogenous AETA application. This genetic deletion also impairs contextual fear memory. Our findings demonstrate AETA-dependent NMDAR activation (ADNA), characterizing AETA as a unique type of endogenous NMDAR modulator that exerts bidirectional control over NMDAR signaling and associated information processing.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter App ; Nmda Receptors ; Amyloid-β Precursor Protein ; Eta-secretase ; Hippocampus ; Long-term Depression ; Memory ; Non-ionotropic Signaling ; Spine Shrinkage ; Synapse; Synaptic Plasticity; Allosteric Modulation; Silent Synapses; Variants; Disease
ISSN (print) / ISBN 0896-6273
e-ISSN 1097-4199
Zeitschrift Neuron
Quellenangaben Band: 112, Heft: 16, Seiten: 2708-2720.e9 Artikelnummer: , Supplement: ,
Verlag Cell Press
Verlagsort Cambridge, Mass.
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Developmental Genetics (IDG)
Förderungen Ministe re de la Recherche, de l'Enseignement Superieur et de l'Innovation
French Association France Alzheimer
French Fondation Alzheimer
Agence Nationale de la Recherche
Flag ERA JTC
Investments for the Future LABEX SIG-NALIFE
Fondation pour la Recherche Medicale (FRM)
European Research Council
Institut Neuromod, Universite Cote d'Azur
MRC
EUFP17 Marie Curie Actions
Wellcome Trust
BBSRC
NIH
Deutsche Forschungsgemeinschaft Walter Benjamin project
Centre National de la Recherche Scientifique (CNRS)