PSD-95-like membrane associated guanylate kinases (PSD-MAGUKs) and synaptic plasticity

Activity-dependent modification of excitatory synaptic transmission is a fundamental mechanism for developmental plasticity of the neural circuits and experience-dependent plasticity. Synaptic glutamatergic receptors including AMPA receptors and NMDA receptors (AMPARs and NMDARs) are embedded in the...

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Bibliographic Details
Main Author: Xu, Weifeng (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences (Contributor), Picower Institute for Learning and Memory (Contributor)
Format: Article
Language:English
Published: Elsevier, 2015-09-18T17:44:50Z.
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Online Access:Get fulltext
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042 |a dc 
100 1 0 |a Xu, Weifeng  |e author 
100 1 0 |a Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences  |e contributor 
100 1 0 |a Picower Institute for Learning and Memory  |e contributor 
100 1 0 |a Xu, Weifeng  |e contributor 
245 0 0 |a PSD-95-like membrane associated guanylate kinases (PSD-MAGUKs) and synaptic plasticity 
260 |b Elsevier,   |c 2015-09-18T17:44:50Z. 
856 |z Get fulltext  |u http://hdl.handle.net/1721.1/98845 
520 |a Activity-dependent modification of excitatory synaptic transmission is a fundamental mechanism for developmental plasticity of the neural circuits and experience-dependent plasticity. Synaptic glutamatergic receptors including AMPA receptors and NMDA receptors (AMPARs and NMDARs) are embedded in the postsynaptic density, a highly organized protein network. Overwhelming data have shown that PSD-95-like membrane associated guanylate kinases (PSD-MAGUKs), a major family of scaffold proteins at glutamatergic synapses, regulate basal synaptic AMPAR function and trafficking. It is now clear that PSD-MAGUKs have multifaceted functions in regulating both basal synaptic transmission and synaptic plasticity. Here we discuss recent advancements in understanding the roles of PSD-95 and other family members of PSD-MAGUKs in synaptic plasticity, both as an anchoring protein for synaptic AMPARs and as a signaling scaffold for mediating the interaction of the signaling complex and NMDARs. 
520 |a National Institute of Mental Health (U.S.) (Grant MH080310) 
546 |a en_US 
655 7 |a Article 
773 |t Current Opinion in Neurobiology