NR3A-containing NMDARs promote neurotransmitter release and spike timing–dependent plasticity

Larsen et al . find that presynaptic NMDA receptors at neocortical synapses are heteromeric receptors containing the developmentally expressed NR3A subunit. Their data also indicate that NR3A-containing presynaptic NMDARs mediate tonic presynaptic activity, synaptic transmission and spike timing–dep...

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Veröffentlicht in:Nature neuroscience 2011-03, Vol.14 (3), p.338-344
Hauptverfasser: Larsen, Rylan S, Corlew, Rebekah J, Henson, Maile A, Roberts, Adam C, Mishina, Masayoshi, Watanabe, Masahiko, Lipton, Stuart A, Nakanishi, Nobuki, Pérez-Otaño, Isabel, Weinberg, Richard J, Philpot, Benjamin D
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container_end_page 344
container_issue 3
container_start_page 338
container_title Nature neuroscience
container_volume 14
creator Larsen, Rylan S
Corlew, Rebekah J
Henson, Maile A
Roberts, Adam C
Mishina, Masayoshi
Watanabe, Masahiko
Lipton, Stuart A
Nakanishi, Nobuki
Pérez-Otaño, Isabel
Weinberg, Richard J
Philpot, Benjamin D
description Larsen et al . find that presynaptic NMDA receptors at neocortical synapses are heteromeric receptors containing the developmentally expressed NR3A subunit. Their data also indicate that NR3A-containing presynaptic NMDARs mediate tonic presynaptic activity, synaptic transmission and spike timing–dependent plasticity. Recent evidence suggests that presynaptic-acting NMDA receptors (preNMDARs) are important for neocortical synaptic transmission and plasticity. We found that unique properties of the NR3A subunit enable preNMDARs to enhance spontaneous and evoked glutamate release and that NR3A is required for spike timing–dependent long-term depression in the juvenile mouse visual cortex. In the mature cortex, NR2B-containing preNMDARs enhanced neurotransmission in the absence of magnesium, indicating that presynaptic NMDARs may function under depolarizing conditions throughout life. Our findings indicate that NR3A relieves preNMDARs from the dual-activation requirement of ligand-binding and depolarization; the developmental removal of NR3A limits preNMDAR functionality by restoring this associative property.
doi_str_mv 10.1038/nn.2750
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subjects 631/378/2591
631/378/2613/1875
631/378/368/2430
631/378/548/1964
Action Potentials - physiology
Animal Genetics and Genomics
Animals
Behavioral Sciences
Biological Techniques
Biomedical and Life Sciences
Biomedicine
Cell receptors
Excitatory Postsynaptic Potentials - physiology
Glutamic Acid - metabolism
Long-Term Synaptic Depression - physiology
Magnesium - metabolism
Methyl aspartate
Mice
Mice, Transgenic
Neurobiology
Neuronal Plasticity - physiology
Neuroplasticity
Neurosciences
Neurotransmitter Agents - metabolism
Neurotransmitters
Protein Subunits - genetics
Protein Subunits - metabolism
Receptors, N-Methyl-D-Aspartate - genetics
Receptors, N-Methyl-D-Aspartate - metabolism
Synaptic Transmission - physiology
Time Factors
title NR3A-containing NMDARs promote neurotransmitter release and spike timing–dependent plasticity
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