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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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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. |
format | Online Article Text |
id | pubmed-10229553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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