Glutamatergic plasticity by synaptic delivery of GluR-B(long)-containing AMPA receptors.

Article Details

Citation

Kolleker A, Zhu JJ, Schupp BJ, Qin Y, Mack V, Borchardt T, Kohr G, Malinow R, Seeburg PH, Osten P

Glutamatergic plasticity by synaptic delivery of GluR-B(long)-containing AMPA receptors.

Neuron. 2003 Dec 18;40(6):1199-212.

PubMed ID
14687553 [ View in PubMed
]
Abstract

Activity-driven delivery of AMPA receptors is proposed to mediate glutamatergic synaptic plasticity, both during development and learning. In hippocampal CA1 principal neurons, such trafficking is primarily mediated by the abundant GluR-A subunit. We now report a study of GluR-B(long), a C-terminal splice variant of the GluR-B subunit. GluR-B(long) synaptic delivery is regulated by two forms of activity. Spontaneous synaptic activity-driven GluR-B(long) transport maintains one-third of the steady-state AMPA receptor-mediated responses, while GluR-B(long) delivery following the induction of LTP is responsible for approximately 50% of the resulting potentiation at the hippocampal CA3 to CA1 synapses at the time of GluR-B(long) peak expression-the second postnatal week. Trafficking of GluR-B(long)-containing receptors thus mediates a GluR-A-independent form of glutamatergic synaptic plasticity in the juvenile hippocampus.

DrugBank Data that Cites this Article

Polypeptides
NameUniProt ID
Glutamate receptor 2P42262Details