Source:http://linkedlifedata.com/resource/pubmed/id/10839540
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6785
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pubmed:dateCreated |
2000-6-16
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pubmed:abstractText |
Activity-dependent change in the efficacy of transmission is a basic feature of many excitatory synapses in the central nervous system. The best understood postsynaptic modification involves a change in responsiveness of AMPAR (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptor)-mediated currents following activation of NMDA (N-methyl-D-aspartate) receptors or Ca2+-permeable AMPARs. This process is thought to involve alteration in the number and phosphorylation state of postsynaptic AMPARs. Here we describe a new form of synaptic plasticity--a rapid and lasting change in the subunit composition and Ca2+ permeability of AMPARs at cerebellar stellate cell synapses following synaptic activity. AMPARs lacking the edited GluR2 subunit not only exhibit high Ca2+ permeability but also are blocked by intracellular polyamines. These properties have allowed us to follow directly the involvement of GluR2 subunits in synaptic transmission. Repetitive synaptic activation of Ca2+-permeable AMPARs causes a rapid reduction in Ca2+ permeability and a change in the amplitude of excitatory postsynaptic currents, owing to the incorporation of GluR2-containing AMPARs. Our experiments show that activity-induced Ca2+ influx through GluR2-lacking AMPARs controls the targeting of GluR2-containing AMPARs, implying the presence of a self-regulating mechanism.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Benzodiazepines,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/GYKI 53655,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, AMPA,
http://linkedlifedata.com/resource/pubmed/chemical/glutamate receptor ionotropic...
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pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
25
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pubmed:volume |
405
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
454-8
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:10839540-Animals,
pubmed-meshheading:10839540-Benzodiazepines,
pubmed-meshheading:10839540-Calcium,
pubmed-meshheading:10839540-Cell Membrane Permeability,
pubmed-meshheading:10839540-Excitatory Amino Acid Antagonists,
pubmed-meshheading:10839540-Excitatory Postsynaptic Potentials,
pubmed-meshheading:10839540-Glutamic Acid,
pubmed-meshheading:10839540-Ion Channel Gating,
pubmed-meshheading:10839540-Neuronal Plasticity,
pubmed-meshheading:10839540-Rats,
pubmed-meshheading:10839540-Rats, Sprague-Dawley,
pubmed-meshheading:10839540-Receptors, AMPA,
pubmed-meshheading:10839540-Synapses,
pubmed-meshheading:10839540-Synaptic Membranes
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pubmed:year |
2000
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pubmed:articleTitle |
Synaptic activity at calcium-permeable AMPA receptors induces a switch in receptor subtype.
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pubmed:affiliation |
Department of Pharmacology, University College London, UK.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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