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Slow AMPA receptors in hippocampal principal cells

Glutamate receptor ion channels, including α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, mediate fast excitatory neurotransmission in the CNS. Previous work suggested that AMPA receptors produce a synaptic current with a millisecond duration. However, we find that about two-...

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Detalles Bibliográficos
Autores principales: Pampaloni, Niccolò P., Riva, Irene, Carbone, Anna L., Plested, Andrew J.R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356020/
https://www.ncbi.nlm.nih.gov/pubmed/34348150
http://dx.doi.org/10.1016/j.celrep.2021.109496
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author Pampaloni, Niccolò P.
Riva, Irene
Carbone, Anna L.
Plested, Andrew J.R.
author_facet Pampaloni, Niccolò P.
Riva, Irene
Carbone, Anna L.
Plested, Andrew J.R.
author_sort Pampaloni, Niccolò P.
collection PubMed
description Glutamate receptor ion channels, including α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, mediate fast excitatory neurotransmission in the CNS. Previous work suggested that AMPA receptors produce a synaptic current with a millisecond duration. However, we find that about two-thirds of principal cells in the hippocampal CA1 region also express AMPA receptors with reduced desensitization that can stay active for half a second after repetitive stimuli. These slow AMPA receptors are expressed at about half of the synapses, with a flat spatial distribution. The increased charge transfer from slow AMPA receptors allows short-term potentiation from a postsynaptic locus and reliable triggering of action potentials. Biophysical and pharmacological observations imply slow AMPA receptors incorporate auxiliary proteins, and their activation lengthens miniature synaptic currents. These data indicate that AMPA receptors are a major source of synaptic diversity. Synapses harboring slow AMPA receptors could have unique roles in hippocampal function.
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spelling pubmed-83560202021-08-15 Slow AMPA receptors in hippocampal principal cells Pampaloni, Niccolò P. Riva, Irene Carbone, Anna L. Plested, Andrew J.R. Cell Rep Article Glutamate receptor ion channels, including α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, mediate fast excitatory neurotransmission in the CNS. Previous work suggested that AMPA receptors produce a synaptic current with a millisecond duration. However, we find that about two-thirds of principal cells in the hippocampal CA1 region also express AMPA receptors with reduced desensitization that can stay active for half a second after repetitive stimuli. These slow AMPA receptors are expressed at about half of the synapses, with a flat spatial distribution. The increased charge transfer from slow AMPA receptors allows short-term potentiation from a postsynaptic locus and reliable triggering of action potentials. Biophysical and pharmacological observations imply slow AMPA receptors incorporate auxiliary proteins, and their activation lengthens miniature synaptic currents. These data indicate that AMPA receptors are a major source of synaptic diversity. Synapses harboring slow AMPA receptors could have unique roles in hippocampal function. Cell Press 2021-08-03 /pmc/articles/PMC8356020/ /pubmed/34348150 http://dx.doi.org/10.1016/j.celrep.2021.109496 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Pampaloni, Niccolò P.
Riva, Irene
Carbone, Anna L.
Plested, Andrew J.R.
Slow AMPA receptors in hippocampal principal cells
title Slow AMPA receptors in hippocampal principal cells
title_full Slow AMPA receptors in hippocampal principal cells
title_fullStr Slow AMPA receptors in hippocampal principal cells
title_full_unstemmed Slow AMPA receptors in hippocampal principal cells
title_short Slow AMPA receptors in hippocampal principal cells
title_sort slow ampa receptors in hippocampal principal cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8356020/
https://www.ncbi.nlm.nih.gov/pubmed/34348150
http://dx.doi.org/10.1016/j.celrep.2021.109496
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