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 |
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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 |
format | Article |
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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.</description><identifier>ISSN: 1097-6256</identifier><identifier>EISSN: 1546-1726</identifier><identifier>DOI: 10.1038/nn.2750</identifier><identifier>PMID: 21297630</identifier><identifier>CODEN: NANEFN</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>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</subject><ispartof>Nature neuroscience, 2011-03, Vol.14 (3), p.338-344</ispartof><rights>Springer Nature America, Inc. 2011</rights><rights>COPYRIGHT 2011 Nature Publishing Group</rights><rights>Copyright Nature Publishing Group Mar 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c540t-d9e858ab78447d10d5e695408cf51336caf4be7b1bd9e8f4185be9a6a22261703</citedby><cites>FETCH-LOGICAL-c540t-d9e858ab78447d10d5e695408cf51336caf4be7b1bd9e8f4185be9a6a22261703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/nn.2750$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/nn.2750$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21297630$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Larsen, Rylan S</creatorcontrib><creatorcontrib>Corlew, Rebekah J</creatorcontrib><creatorcontrib>Henson, Maile A</creatorcontrib><creatorcontrib>Roberts, Adam C</creatorcontrib><creatorcontrib>Mishina, Masayoshi</creatorcontrib><creatorcontrib>Watanabe, Masahiko</creatorcontrib><creatorcontrib>Lipton, Stuart A</creatorcontrib><creatorcontrib>Nakanishi, Nobuki</creatorcontrib><creatorcontrib>Pérez-Otaño, Isabel</creatorcontrib><creatorcontrib>Weinberg, Richard J</creatorcontrib><creatorcontrib>Philpot, Benjamin D</creatorcontrib><title>NR3A-containing NMDARs promote neurotransmitter release and spike timing–dependent plasticity</title><title>Nature neuroscience</title><addtitle>Nat Neurosci</addtitle><addtitle>Nat Neurosci</addtitle><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.</description><subject>631/378/2591</subject><subject>631/378/2613/1875</subject><subject>631/378/368/2430</subject><subject>631/378/548/1964</subject><subject>Action Potentials - physiology</subject><subject>Animal Genetics and Genomics</subject><subject>Animals</subject><subject>Behavioral Sciences</subject><subject>Biological Techniques</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cell receptors</subject><subject>Excitatory Postsynaptic Potentials - physiology</subject><subject>Glutamic Acid - metabolism</subject><subject>Long-Term Synaptic Depression - physiology</subject><subject>Magnesium - metabolism</subject><subject>Methyl aspartate</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Neurobiology</subject><subject>Neuronal Plasticity - 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Academic</collection><jtitle>Nature neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Larsen, Rylan S</au><au>Corlew, Rebekah J</au><au>Henson, Maile A</au><au>Roberts, Adam C</au><au>Mishina, Masayoshi</au><au>Watanabe, Masahiko</au><au>Lipton, Stuart A</au><au>Nakanishi, Nobuki</au><au>Pérez-Otaño, Isabel</au><au>Weinberg, Richard J</au><au>Philpot, Benjamin D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>NR3A-containing NMDARs promote neurotransmitter release and spike timing–dependent plasticity</atitle><jtitle>Nature neuroscience</jtitle><stitle>Nat Neurosci</stitle><addtitle>Nat Neurosci</addtitle><date>2011-03-01</date><risdate>2011</risdate><volume>14</volume><issue>3</issue><spage>338</spage><epage>344</epage><pages>338-344</pages><issn>1097-6256</issn><eissn>1546-1726</eissn><coden>NANEFN</coden><abstract>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.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>21297630</pmid><doi>10.1038/nn.2750</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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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