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Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway
Bouts of high frequency activity known as sharp wave ripples (SPW-Rs) facilitate communication between the hippocampus and neocortex. However, the paths and mechanisms by which SPW-Rs broadcast their content are not well understood. Due to its anatomical positioning, the granular retrosplenial corte...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181800/ https://www.ncbi.nlm.nih.gov/pubmed/32327634 http://dx.doi.org/10.1038/s41467-020-15787-8 |
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author | Nitzan, Noam McKenzie, Sam Beed, Prateep English, Daniel Fine Oldani, Silvia Tukker, John J. Buzsáki, György Schmitz, Dietmar |
author_facet | Nitzan, Noam McKenzie, Sam Beed, Prateep English, Daniel Fine Oldani, Silvia Tukker, John J. Buzsáki, György Schmitz, Dietmar |
author_sort | Nitzan, Noam |
collection | PubMed |
description | Bouts of high frequency activity known as sharp wave ripples (SPW-Rs) facilitate communication between the hippocampus and neocortex. However, the paths and mechanisms by which SPW-Rs broadcast their content are not well understood. Due to its anatomical positioning, the granular retrosplenial cortex (gRSC) may be a bridge for this hippocampo-cortical dialogue. Using silicon probe recordings in awake, head-fixed mice, we show the existence of SPW-R analogues in gRSC and demonstrate their coupling to hippocampal SPW-Rs. gRSC neurons reliably distinguished different subclasses of hippocampal SPW-Rs according to ensemble activity patterns in CA1. We demonstrate that this coupling is brain state-dependent, and delineate a topographically-organized anatomical pathway via VGlut2-expressing, bursty neurons in the subiculum. Optogenetic stimulation or inhibition of bursty subicular cells induced or reduced responses in superficial gRSC, respectively. These results identify a specific path and underlying mechanisms by which the hippocampus can convey neuronal content to the neocortex during SPW-Rs. |
format | Online Article Text |
id | pubmed-7181800 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71818002020-04-29 Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway Nitzan, Noam McKenzie, Sam Beed, Prateep English, Daniel Fine Oldani, Silvia Tukker, John J. Buzsáki, György Schmitz, Dietmar Nat Commun Article Bouts of high frequency activity known as sharp wave ripples (SPW-Rs) facilitate communication between the hippocampus and neocortex. However, the paths and mechanisms by which SPW-Rs broadcast their content are not well understood. Due to its anatomical positioning, the granular retrosplenial cortex (gRSC) may be a bridge for this hippocampo-cortical dialogue. Using silicon probe recordings in awake, head-fixed mice, we show the existence of SPW-R analogues in gRSC and demonstrate their coupling to hippocampal SPW-Rs. gRSC neurons reliably distinguished different subclasses of hippocampal SPW-Rs according to ensemble activity patterns in CA1. We demonstrate that this coupling is brain state-dependent, and delineate a topographically-organized anatomical pathway via VGlut2-expressing, bursty neurons in the subiculum. Optogenetic stimulation or inhibition of bursty subicular cells induced or reduced responses in superficial gRSC, respectively. These results identify a specific path and underlying mechanisms by which the hippocampus can convey neuronal content to the neocortex during SPW-Rs. Nature Publishing Group UK 2020-04-23 /pmc/articles/PMC7181800/ /pubmed/32327634 http://dx.doi.org/10.1038/s41467-020-15787-8 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Nitzan, Noam McKenzie, Sam Beed, Prateep English, Daniel Fine Oldani, Silvia Tukker, John J. Buzsáki, György Schmitz, Dietmar Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title | Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title_full | Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title_fullStr | Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title_full_unstemmed | Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title_short | Propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
title_sort | propagation of hippocampal ripples to the neocortex by way of a subiculum-retrosplenial pathway |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7181800/ https://www.ncbi.nlm.nih.gov/pubmed/32327634 http://dx.doi.org/10.1038/s41467-020-15787-8 |
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