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Title:
NMDA receptor function: subunit composition versus spatial distribution | Cell and Tissue Research
Description:
NMDA receptors (NMDARs) play a pivotal role in the regulation of neuronal communication and synaptic function in the central nervous system. The subunit composition and compartmental localization of NMDARs in neurons affect channel activity and downstream signaling. This review discusses the distinct NMDAR subtypes and their function at synaptic, perisynaptic, and extrasynaptic sites of excitatory and inhibitory neurons. Many neurons express more than one of the modulatory NR2 subunits that participate in the formation of di- and/or triheteromeric channel assemblies (e.g., NR1/NR2A, NR1/NR2B, and/or NR1/NR2A/NR2B). Depending on the subunit composition and presence or absence of intracellular binding partners along the postsynaptic membrane, these NMDAR subtypes are allocated to distinct synaptic inputs converging onto a neuron or are distributed differentially among synaptic or extrasynaptic sites. These sites can carry NR2A and NR2B subunits, supporting the hypothesis that the spatial distribution of scaffolding and signaling complexes critically determines the full spectrum of NMDAR signaling.
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Keywords {๐}
google, scholar, cas, pubmed, nmda, receptors, neurosci, receptor, synaptic, subunit, extrasynaptic, nrb, subunits, neuron, glutamate, rat, distinct, synapses, cell, neurons, nat, hippocampal, composition, longterm, nmethyldaspartate, physiol, lond, function, article, kรถhr, nature, signaling, subtypes, functional, plasticity, potentiation, mishina, pharmacol, wang, trafficking, content, research, regulation, nra, channels, cells, properties, inhibition, developing, cortical,
Topics {โ๏ธ}
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headline:NMDA receptor function: subunit composition versus spatial distribution
description:NMDA receptors (NMDARs) play a pivotal role in the regulation of neuronal communication and synaptic function in the central nervous system. The subunit composition and compartmental localization of NMDARs in neurons affect channel activity and downstream signaling. This review discusses the distinct NMDAR subtypes and their function at synaptic, perisynaptic, and extrasynaptic sites of excitatory and inhibitory neurons. Many neurons express more than one of the modulatory NR2 subunits that participate in the formation of di- and/or triheteromeric channel assemblies (e.g., NR1/NR2A, NR1/NR2B, and/or NR1/NR2A/NR2B). Depending on the subunit composition and presence or absence of intracellular binding partners along the postsynaptic membrane, these NMDAR subtypes are allocated to distinct synaptic inputs converging onto a neuron or are distributed differentially among synaptic or extrasynaptic sites. These sites can carry NR2A and NR2B subunits, supporting the hypothesis that the spatial distribution of scaffolding and signaling complexes critically determines the full spectrum of NMDAR signaling.
datePublished:2006-07-22T00:00:00Z
dateModified:2006-07-22T00:00:00Z
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NMDA receptors
Subtype
Extrasynaptic
Triheteromeric
Pharmacology
Signaling
Human Genetics
Proteomics
Molecular Medicine
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headline:NMDA receptor function: subunit composition versus spatial distribution
description:NMDA receptors (NMDARs) play a pivotal role in the regulation of neuronal communication and synaptic function in the central nervous system. The subunit composition and compartmental localization of NMDARs in neurons affect channel activity and downstream signaling. This review discusses the distinct NMDAR subtypes and their function at synaptic, perisynaptic, and extrasynaptic sites of excitatory and inhibitory neurons. Many neurons express more than one of the modulatory NR2 subunits that participate in the formation of di- and/or triheteromeric channel assemblies (e.g., NR1/NR2A, NR1/NR2B, and/or NR1/NR2A/NR2B). Depending on the subunit composition and presence or absence of intracellular binding partners along the postsynaptic membrane, these NMDAR subtypes are allocated to distinct synaptic inputs converging onto a neuron or are distributed differentially among synaptic or extrasynaptic sites. These sites can carry NR2A and NR2B subunits, supporting the hypothesis that the spatial distribution of scaffolding and signaling complexes critically determines the full spectrum of NMDAR signaling.
datePublished:2006-07-22T00:00:00Z
dateModified:2006-07-22T00:00:00Z
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pageEnd:446
sameAs:https://doi.org/10.1007/s00441-006-0273-6
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NMDA receptors
Subtype
Extrasynaptic
Triheteromeric
Pharmacology
Signaling
Human Genetics
Proteomics
Molecular Medicine
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