| Literature DB >> 29224722 |
Ning Lei1, Jerry E Mellem1, Penelope J Brockie1, David M Madsen1, Andres V Maricq2.
Abstract
NMDA receptors (NMDARs) are a subtype of postsynaptic ionotropic glutamate receptors that function as molecular coincidence detectors, have critical roles in models of learning, and are associated with a variety of neurological and psychiatric disorders. To date, no auxiliary proteins that modify NMDARs have been identified. Here, we report the identification of NRAP-1, an auxiliary protein in C. elegans that modulates NMDAR function. NMDAR-mediated currents were eliminated in nrap-1 mutants, as was NMDA-dependent behavior. We show that reconstitution of NMDA-gated current in Xenopus oocytes, or C. elegans muscle cells, depends on NRAP-1 and that recombinant NRAP-1 can convert silent NMDARs to functional channels. Our data indicate that NRAP-1, secreted from presynaptic neurons, localizes to glutamatergic synapses, where it associates with postsynaptic NMDARs to modify receptor gating. Thus, our studies reveal a novel mechanism for synaptic regulation via pre-synaptic control of NMDAR-mediated synaptic transmission.Entities:
Keywords: NMDA receptor; auxiliary protein; glutamate; iGluR; learning and memory; receptor desensitization; silent synapse; synaptic plasticity
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Year: 2017 PMID: 29224722 PMCID: PMC8819664 DOI: 10.1016/j.neuron.2017.11.019
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173