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Afferent convergence to a shared population of interneuron AMPA receptors

Precise alignment of pre- and postsynaptic elements optimizes the activation of glutamate receptors at excitatory synapses. Nonetheless, glutamate that diffuses out of the synaptic cleft can have actions at distant receptors, a mode of transmission called spillover. To uncover the extrasynaptic acti...

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Autores principales: Pennock, Reagan L., Coddington, Luke T., Yan, Xiaohui, Overstreet-Wadiche, Linda, Wadiche, Jacques I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229553/
https://www.ncbi.nlm.nih.gov/pubmed/37253743
http://dx.doi.org/10.1038/s41467-023-38854-2
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author Pennock, Reagan L.
Coddington, Luke T.
Yan, Xiaohui
Overstreet-Wadiche, Linda
Wadiche, Jacques I.
author_facet Pennock, Reagan L.
Coddington, Luke T.
Yan, Xiaohui
Overstreet-Wadiche, Linda
Wadiche, Jacques I.
author_sort Pennock, Reagan L.
collection PubMed
description Precise alignment of pre- and postsynaptic elements optimizes the activation of glutamate receptors at excitatory synapses. Nonetheless, glutamate that diffuses out of the synaptic cleft can have actions at distant receptors, a mode of transmission called spillover. To uncover the extrasynaptic actions of glutamate, we localized AMPA receptors (AMPARs) mediating spillover transmission between climbing fibers and molecular layer interneurons in the cerebellar cortex. We found that climbing fiber spillover generates calcium transients mediated by Ca(2+)-permeable AMPARs at parallel fiber synapses. Spillover occludes parallel fiber synaptic currents, indicating that separate, independently regulated afferent pathways converge onto a common pool of AMPARs. Together these findings demonstrate a circuit motif wherein glutamate ‘spill-in’ from an unconnected afferent pathway co-opts synaptic receptors, allowing activation of postsynaptic AMPARs even when canonical glutamate release is suppressed.
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spelling pubmed-102295532023-06-01 Afferent convergence to a shared population of interneuron AMPA receptors Pennock, Reagan L. Coddington, Luke T. Yan, Xiaohui Overstreet-Wadiche, Linda Wadiche, Jacques I. Nat Commun Article Precise alignment of pre- and postsynaptic elements optimizes the activation of glutamate receptors at excitatory synapses. Nonetheless, glutamate that diffuses out of the synaptic cleft can have actions at distant receptors, a mode of transmission called spillover. To uncover the extrasynaptic actions of glutamate, we localized AMPA receptors (AMPARs) mediating spillover transmission between climbing fibers and molecular layer interneurons in the cerebellar cortex. We found that climbing fiber spillover generates calcium transients mediated by Ca(2+)-permeable AMPARs at parallel fiber synapses. Spillover occludes parallel fiber synaptic currents, indicating that separate, independently regulated afferent pathways converge onto a common pool of AMPARs. Together these findings demonstrate a circuit motif wherein glutamate ‘spill-in’ from an unconnected afferent pathway co-opts synaptic receptors, allowing activation of postsynaptic AMPARs even when canonical glutamate release is suppressed. Nature Publishing Group UK 2023-05-30 /pmc/articles/PMC10229553/ /pubmed/37253743 http://dx.doi.org/10.1038/s41467-023-38854-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Pennock, Reagan L.
Coddington, Luke T.
Yan, Xiaohui
Overstreet-Wadiche, Linda
Wadiche, Jacques I.
Afferent convergence to a shared population of interneuron AMPA receptors
title Afferent convergence to a shared population of interneuron AMPA receptors
title_full Afferent convergence to a shared population of interneuron AMPA receptors
title_fullStr Afferent convergence to a shared population of interneuron AMPA receptors
title_full_unstemmed Afferent convergence to a shared population of interneuron AMPA receptors
title_short Afferent convergence to a shared population of interneuron AMPA receptors
title_sort afferent convergence to a shared population of interneuron ampa receptors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10229553/
https://www.ncbi.nlm.nih.gov/pubmed/37253743
http://dx.doi.org/10.1038/s41467-023-38854-2
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