Receptor trafficking and synaptic plasticity

By G. Collingridge, J. Isaac, Y. Wang. Nature Reviews Neuroscience, 2004

1,060 citations recorded by the source corpus.

Subfields: Cellular and Molecular Neuroscience, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/21c6cbb9201f3530e0dddaa230587f433226a816

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In Cellular and Molecular Neuroscience

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Citations in the corpus

Mechanisms of neuronal cell death in ischemic stroke and their therapeutic implications (2021, background): “The two major subtypes of ionotropic glutamate receptors are the N‐methyl‐D‐aspartate receptors (NMDARs) and the α‐amino‐3‐hydroxy‐5‐methyl‐4‐isoxazole propionic acid receptors (AMPARs).(29) Pre‐synaptic release of”
The cell biology of synaptic plasticity: AMPA receptor trafficking. (2007, background): “A full review of the LTP/LTD literature is beyond the scope of this article (for further reading, see Bredt & Nicoll 2003, Collingridge et al. 2004, Song & Huganir 2002).”
NMDA receptor-dependent long-term potentiation and long-term depression (LTP/LTD). (2012, background): “A large body of experimental evidence now supports this hypothesis (Lüscher et al. 2000; Lüscher and Frerking 2001; Malinow and Malenka 2002; Nicoll 2003; Collingridge et al. 2004; Malenka and Bear 2004).”
Molecular and electrophysiological evidence for net synaptic potentiation in wake and depression in sleep (2008, background): “At the molecular level, the best established mechanism for the expression of LTP and LTD involves the trafficking of postsynaptic glutamatergic AMPARs containing the GluR1 subuni”
LTP inhibits LTD in the hippocampus via regulation of GSK3beta. (2007, positive): “Cells were lysed as before and coimmunoprecipitated for 2-4 hrs at 4  C with a mouse GluR2 N-terminal monocolonal antibody (10  g/mL; Chemicon) bound to Protein G-sepharose beads.”
Protein palmitoylation in neuronal development and synaptic plasticity (2010, background): “Because the number of AMPARs at the postsynaptic terminal determines the efficacy of excitatory synaptic transmission, the molecular mechanisms underlying AMPAR trafficking are thought to have a central role in synaptic plasticit”
Concepts of neural nitric oxide-mediated transmission (2008, background): “…classes of nNOS-containing GABAergic interneurone that innervate the microvasculature (Yang et al., 2000; Cauli et al., 2004; Rancillac et al., 2006), with NO working alongside several other local constrictor and dilator molecules, including peptides and prostanoids (reviewed by Iadecola, 2004).”
Antibodies to the GABAB receptor in limbic encephalitis with seizures: case series and characterisation of the antigen (2009, background): “Redistribution of GABAB(1) protein and atypical GABAB responses in GABAB(2)-deficient mice.”
Synaptic Plasticity: Multiple Forms, Functions, and Mechanisms (2008, background): “Although these subunits are highly homologous, both the functional properties of AMPARs and their trafficking has been suggested to depend on their subunit composition (Collingridge et al, 2004; Derkach et al, 2007; Malinow and Malenka, 2002).”
Subunit composition of synaptic AMPA receptors revealed by a single-cell genetic approach (2009, neutral): “In contrast, a number of studies have suggested that the GluA2subunitdictatestheremovalofAMPARsfromthesynapse during LTD (Bredt and Nicoll, 2003; Collingridge et al., 2004; Malinow and Malenka, 2002; Shepherd and Huganir, 2007).”
Glutamate Receptor Ion Channels: Structure, Regulation, and Function (2010, background): “Several excellent reviews on these protein-protein interactions exist (Collingridge et al., 2004; Malenka and Bear, 2004; Shepherd and Huganir, 2007; Ashby et al., 2008; Pelkey and McBain, 2008).”
Regulatory mechanisms of AMPA receptors in synaptic plasticity (2007, background): “Although these subunits are highly homologous, both the functional properties of AMPARs and their trafficking depend on subunit compositio”
Long-term depression in the CNS (2010, background): “Although genetic and pharmacological studies have suggested that NMDAR-LTD of AMPAR-mediated synaptic transmission (LTD(A)) involves the activation of specific NMDAR subtype”
Sleep and synaptic renormalization: a computational study. (2010, background): “Although both NMDA and GABA receptors (NMDAR, GABAR) 294 have been show to undergo plastic modifications, most studies have focused on their role in modulating 295 AMPAR plasticity (Collingridge et al. 2004).”