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Neuronal sequences during theta rely on behavior-dependent spatial maps
Navigation through space involves learning and representing relationships between past, current, and future locations. In mammals, this might rely on the hippocampal theta phase code, where in each cycle of the theta oscillation, spatial representations provided by neuronal sequences start behind th...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565928/ https://www.ncbi.nlm.nih.gov/pubmed/34661526 http://dx.doi.org/10.7554/eLife.70296 |
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author | Parra-Barrero, Eloy Diba, Kamran Cheng, Sen |
author_facet | Parra-Barrero, Eloy Diba, Kamran Cheng, Sen |
author_sort | Parra-Barrero, Eloy |
collection | PubMed |
description | Navigation through space involves learning and representing relationships between past, current, and future locations. In mammals, this might rely on the hippocampal theta phase code, where in each cycle of the theta oscillation, spatial representations provided by neuronal sequences start behind the animal’s true location and then sweep forward. However, the exact relationship between theta phase, represented position and true location remains unclear and even paradoxical. Here, we formalize previous notions of ‘spatial’ or ‘temporal’ theta sweeps that have appeared in the literature. We analyze single-cell and population variables in unit recordings from rat CA1 place cells and compare them to model simulations based on each of these schemes. We show that neither spatial nor temporal sweeps quantitatively accounts for how all relevant variables change with running speed. To reconcile these schemes with our observations, we introduce ‘behavior-dependent’ sweeps, in which theta sweep length and place field properties, such as size and phase precession, vary across the environment depending on the running speed characteristic of each location. These behavior-dependent spatial maps provide a structured heterogeneity that is essential for understanding the hippocampal code. |
format | Online Article Text |
id | pubmed-8565928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-85659282021-11-04 Neuronal sequences during theta rely on behavior-dependent spatial maps Parra-Barrero, Eloy Diba, Kamran Cheng, Sen eLife Neuroscience Navigation through space involves learning and representing relationships between past, current, and future locations. In mammals, this might rely on the hippocampal theta phase code, where in each cycle of the theta oscillation, spatial representations provided by neuronal sequences start behind the animal’s true location and then sweep forward. However, the exact relationship between theta phase, represented position and true location remains unclear and even paradoxical. Here, we formalize previous notions of ‘spatial’ or ‘temporal’ theta sweeps that have appeared in the literature. We analyze single-cell and population variables in unit recordings from rat CA1 place cells and compare them to model simulations based on each of these schemes. We show that neither spatial nor temporal sweeps quantitatively accounts for how all relevant variables change with running speed. To reconcile these schemes with our observations, we introduce ‘behavior-dependent’ sweeps, in which theta sweep length and place field properties, such as size and phase precession, vary across the environment depending on the running speed characteristic of each location. These behavior-dependent spatial maps provide a structured heterogeneity that is essential for understanding the hippocampal code. eLife Sciences Publications, Ltd 2021-10-18 /pmc/articles/PMC8565928/ /pubmed/34661526 http://dx.doi.org/10.7554/eLife.70296 Text en © 2021, Parra-Barrero et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Parra-Barrero, Eloy Diba, Kamran Cheng, Sen Neuronal sequences during theta rely on behavior-dependent spatial maps |
title | Neuronal sequences during theta rely on behavior-dependent spatial maps |
title_full | Neuronal sequences during theta rely on behavior-dependent spatial maps |
title_fullStr | Neuronal sequences during theta rely on behavior-dependent spatial maps |
title_full_unstemmed | Neuronal sequences during theta rely on behavior-dependent spatial maps |
title_short | Neuronal sequences during theta rely on behavior-dependent spatial maps |
title_sort | neuronal sequences during theta rely on behavior-dependent spatial maps |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8565928/ https://www.ncbi.nlm.nih.gov/pubmed/34661526 http://dx.doi.org/10.7554/eLife.70296 |
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