The AMPA Receptor Code of Synaptic Plasticity

• Published in: Neuron (Cambridge, Mass.) Mass.), 2018-10, Vol.100 (2), p.314-329
• Main Authors: Diering, Graham H., Huganir, Richard L.
• Format: Article
• Language: English
• Subjects: Animals; Brain - physiology; Computer applications; Epigenetics; Gene expression; Glutamate receptors; Homeostatic plasticity; homeostatic scaling; Humans; Hypotheses; Information processing; Information storage; learning; Long-term depression; Long-term potentiation; memory; Neuronal Plasticity - physiology; NMDA receptors; Phosphorylation; Proteins; Receptor mechanisms; Receptors, AMPA - physiology; Scaling; Synapses; Synapses - physiology; Synaptic plasticity; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid; α-Amino-3-hydroxy-5-methyl-4-isoxazole propionic acid receptors
• ISSN: 0896-6273; 1097-4199
• DOI: 10.1016/j.neuron.2018.10.018

Changes in the properties and postsynaptic abundance of AMPA-type glutamate receptors (AMPARs) are major mechanisms underlying various forms of synaptic plasticity, including long-term potentiation (LTP), long-term depression (LTD), and homeostatic scaling. The function and the trafficking of AMPARs to and from synapses is modulated by specific AMPAR GluA1–GluA4 subunits, subunit-specific protein interactors, auxiliary subunits, and posttranslational modifications. Layers of regulation are added to AMPAR tetramers through these different interactions and modifications, increasing the computational power of synapses. Here we review the reliance of synaptic plasticity on AMPAR variants and propose “the AMPAR code” as a conceptual framework. The AMPAR code suggests that AMPAR variants will be predictive of the types and extent of synaptic plasticity that can occur and that a hierarchy exists such that certain AMPARs will be disproportionally recruited to synapses during LTP/homeostatic scaling up, or removed during LTD/homeostatic scaling down. Changes in the number and properties of postsynaptic AMPARs are a fundamental mechanism of synaptic plasticity. Diering and Huganir discuss how AMPAR subunits, posttranslational modifications, and protein binding partners form combinatorial molecular codes relevant for understanding synapse function and plasticity.