4.6 Article

Synaptic NMDA receptor activity at resting membrane potentials

Journal

FRONTIERS IN CELLULAR NEUROSCIENCE
Volume 16, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fncel.2022.916626

Keywords

NMDA receptors; glutamate; somatosensory cortex; hippocampus; postsynaptic signaling

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NMDA receptors (NMDARs) play a crucial role in glutamatergic synaptic signaling in the mammalian central nervous system. The unique biophysical properties of NMDARs, including their ligand- and voltage-dependence, allow them to function as synaptic coincidence detectors, controlling the influx of synaptic Ca2+. Experimental results show that NMDARs contribute to synaptic currents and Ca2+ influx even in the presence of extracellular Mg2+ and absence of AMPAR depolarization. This suggests that NMDARs have an important role in synaptic signaling.
NMDA receptors (NMDARs) are crucial for glutamatergic synaptic signaling in the mammalian central nervous system. When activated by glutamate and glycine/D-serine, the NMDAR ion channel can open, but current flux is further regulated by voltage-dependent block conferred by extracellular Mg2+ ions. The unique biophysical property of ligand- and voltage-dependence positions NMDARs as synaptic coincidence detectors, controlling a major source of synaptic Ca2+ influx. We measured synaptic currents in layer 2/3 neurons after stimulation in layer 4 of somatosensory cortex and found measurable NMDAR currents at all voltages tested. This NMDAR current did not require concurrent AMPAR depolarization. In physiological ionic conditions, the NMDAR current response at negative potentials was enhanced relative to ionic conditions typically used in slice experiments. NMDAR activity was also seen in synaptic recordings from hippocampal CA1 neurons, indicating a general property of NMDAR signaling. Using a fluorescent Ca2+ indicator, we measured responses to stimulation in layer 4 at individual synaptic sites, and Ca2+ influx could be detected even with AMPARs blocked. In current clamp recordings, we found that resting membrane potential was hyperpolarized by similar to 7 mV and AP firing threshold depolarized by similar to 4 mV in traditional compared to physiological ionic concentrations, and that NMDARs contribute to EPSPs at resting membrane potentials. These measurements demonstrate that, even in the presence of extracellular Mg2+ and absence of postsynaptic depolarization, NMDARs contribute to synaptic currents and Ca2+ influx.

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