Colocalization of distinct NMDA receptor subtypes at excitatory synapses in the entorhinal cortex

• Published in: Journal of neurophysiology Vol. 121; no. 1; pp. 238 - 254
• Main Authors: Beesley, Stephen, Sullenberger, Thomas, Pilli, Jyotsna, Abbasi, Saad, Gunjan, Akash, Kumar, Sanjay S
• Format: Journal Article
• Language: English
• Published: United States American Physiological Society 01.01.2019
• Series: Cellular and Molecular Properties of Neurons
• Subjects: Animals; Entorhinal Cortex - cytology; Entorhinal Cortex - drug effects; Entorhinal Cortex - metabolism; Gene Expression; Male; Membrane Potentials - drug effects; Membrane Potentials - physiology; Neurons - cytology; Neurons - drug effects; Neurons - metabolism; Neurotransmitter Agents - pharmacology; Rats, Sprague-Dawley; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors; Receptors, N-Methyl-D-Aspartate - metabolism; Synapses - drug effects; Synapses - metabolism; Tissue Culture Techniques; entorhinal cortex; triheteromeric NMDA receptors; synapse specificity of NMDA receptor subunit composition; electrophysiology
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00468.2018

The subunit composition of N-methyl-d-aspartate receptors (NMDARs) at synaptic inputs onto a neuron can either vary or be uniform depending on the type of neuron and/or brain region. Excitatory pyramidal neurons in the frontal and somatosensory cortices (L5), for example, show pathway-specific differences in NMDAR subunit composition in contrast with the entorhinal cortex (L3), where we now show colocalization of NMDARs with distinct subunit compositions at individual synaptic inputs onto these neurons. Subunit composition was deduced electrophysiologically based on alterations of current-voltage relationship ( I-V) profiles, amplitudes, and decay kinetics of minimally evoked, pharmacologically isolated, NMDAR-mediated excitatory postsynaptic currents by known subunit-preferring antagonists. The I-Vs were outwardly rectifying in a majority of neurons assayed (~80%), indicating expression of GluN1/GluN2/GluN3-containing triheteromeric NMDARs ( t-NMDARs) and of the conventional type, reversing close to 0 mV with prominent regions of negative slope, in the rest of the neurons sampled (~20%), indicating expression of GluN1/GluN2-containing diheteromeric NMDARs ( d-NMDARs). Blocking t-NMDARs in neurons with outwardly rectifying I-Vs pharmacologically unmasked d-NMDARs, with all responses antagonized using D-AP5. Coimmunoprecipitation assays of membrane-bound protein complexes isolated from the medial entorhinal area using subunit-selective antibodies corroborated stoichiometry and together suggested the coexpression of t- and d-NMDARs at these synapses. Colocalization of functionally distinct NMDAR subtypes at individual synaptic inputs likely enhances the repertoire of pyramidal neurons for information processing and plasticity within the entorhinal cortex. NEW & NOTEWORTHY The subunit composition of a N-methyl-d-aspartate (NMDA) receptor, which dictates most aspects of its function, can vary between neurons in different brain regions and/or between synaptic inputs onto single neurons. Here we demonstrate colocalization of tri- and diheteromeric-NMDA receptors at the same/single synaptic input onto excitatory neurons in the entorhinal cortex. Synaptic colocalization of distinct NMDAR subtypes might endow entorhinal cortical neurons with the ability to encode distinct patterns of neuronal activity through single synapses.