4.7 Article

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

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NATURE NEUROSCIENCE
卷 14, 期 3, 页码 338-344

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NATURE PUBLISHING GROUP
DOI: 10.1038/nn.2750

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资金

  1. National Alliance for Research on Schizophrenia and Depression
  2. Marie Curie International Program, UTE project Centro de Investigacion Medica Aplicada
  3. Spanish Ministry of Education and Science [SAF2006-10025, CSD2008-00005]
  4. National Research Service Award [F31 GM080162]
  5. University of North Carolina
  6. National Institute of Child Health and Human Development [T32 HD40127]
  7. NARSAD
  8. US National Institutes of Health [RO1 NS39444]
  9. NARSAD, NEI [R01 EY018323]
  10. National Science Foundation [0822969, P01 HD29587, R01 EY05477, R01 EY09024]
  11. Division Of Integrative Organismal Systems
  12. Direct For Biological Sciences [0822969] Funding Source: National Science Foundation
  13. Grants-in-Aid for Scientific Research [21249012, 19100005] Funding Source: KAKEN

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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.

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