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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...

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Detalles Bibliográficos
Autores principales: Parra-Barrero, Eloy, Diba, Kamran, Cheng, Sen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
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.
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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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