Age‐dependent NMDA receptor function is regulated by the amyloid precursor protein. Issue 3 (26th January 2023)

• Record Type: Journal Article
• Authors: Rajão‐Saraiva, Joana; Dunot, Jade; Ribera, Aurore; Temido‐Ferreira, Mariana; Coelho, Joana E.; König, Svenja; Moreno, Sébastien; Enguita, Francisco J.; Willem, Michael; Kins, Stefan; Marie, Hélène; Lopes, Luísa V.; Pousinha, Paula A.
• Is Part Of: Aging cell. Volume 22:Issue 3(2023)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2023-01-26
• Subjects: aging -- AICD -- Alzheimer's disease -- APP -- excitatory synapse -- Fe65 -- GluN2B -- hippocampus -- NMDA receptor -- postnatal development; Cells -- Aging -- Periodicals; 571.8783605
• DOI: 10.1111/acel.13778
• Languages: English
• ISSNs: 1474-9718

Abstract

Abstract: N‐methyl‐D‐aspartate receptors (NMDARs) are critical for the maturation and plasticity of glutamatergic synapses. In the hippocampus, NMDARs mainly contain GluN2A and/or GluN2B regulatory subunits. The amyloid precursor protein (APP) has emerged as a putative regulator of NMDARs, but the impact of this interaction to their function is largely unknown. By combining patch‐clamp electrophysiology and molecular approaches, we unravel a dual mechanism by which APP controls GluN2B‐NMDARs, depending on the life stage. We show that APP is highly abundant specifically at the postnatal postsynapse. It interacts with GluN2B‐NMDARs, controlling its synaptic content and mediated currents, both in infant mice and primary neuronal cultures. Upon aging, the APP amyloidogenic‐derived C‐terminal fragments, rather than APP full‐length, contribute to aberrant GluN2B‐NMDAR currents. Accordingly, we found that the APP processing is increased upon aging, both in mice and human brain. Interfering with stability or production of the APP intracellular domain normalized the GluN2B‐NMDARs currents. While the first mechanism might be essential for synaptic maturation during development, the latter could contribute to age‐related synaptic impairments. Abstract : Rajão‐Saraiva et al. identified the amyloid precursor protein (APP) as an important regulator of NMDA receptors, acting through a dual age‐dependent mechanism. During postnatal development, APP controls GluN2B‐NMDAR synaptic content and currents, potentially contributing to synaptic maturation. Upon aging, the APP amyloidogenic intracellular fragments contribute to aberrant GluN2B‐NMDAR currents. This work highlights the importance of keeping APP processing under tight control, to ensure the normal functioning of glutamatergic synapses, being particularly relevant to understand age‐related synaptic impairments and Alzheimer's disease.