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Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior

Homing based on path integration (H-PI) is a form of navigation in which an animal uses self-motion cues to keep track of its position and return to a starting point. Despite evidence for a role of the hippocampus in homing behavior, the hippocampal spatial representations associated with H-PI are l...

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Autores principales: Najafian Jazi, Maryam, Tymorek, Adrian, Yen, Ting-Yun, Jose Kavarayil, Felix, Stingl, Moritz, Chau, Sherman Richard, Baskurt, Benay, García Vilela, Celia, Allen, Kevin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651862/
https://www.ncbi.nlm.nih.gov/pubmed/37968268
http://dx.doi.org/10.1038/s41467-023-42642-3
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author Najafian Jazi, Maryam
Tymorek, Adrian
Yen, Ting-Yun
Jose Kavarayil, Felix
Stingl, Moritz
Chau, Sherman Richard
Baskurt, Benay
García Vilela, Celia
Allen, Kevin
author_facet Najafian Jazi, Maryam
Tymorek, Adrian
Yen, Ting-Yun
Jose Kavarayil, Felix
Stingl, Moritz
Chau, Sherman Richard
Baskurt, Benay
García Vilela, Celia
Allen, Kevin
author_sort Najafian Jazi, Maryam
collection PubMed
description Homing based on path integration (H-PI) is a form of navigation in which an animal uses self-motion cues to keep track of its position and return to a starting point. Despite evidence for a role of the hippocampus in homing behavior, the hippocampal spatial representations associated with H-PI are largely unknown. Here we developed a homing task (AutoPI task) that required a mouse to find a randomly placed lever on an arena before returning to its home base. Recordings from the CA1 area in male mice showed that hippocampal neurons remap between random foraging and AutoPI task, between trials in light and dark conditions, and between search and homing behavior. During the AutoPI task, approximately 25% of the firing fields were anchored to the lever position. The activity of 24% of the cells with a lever-anchored field predicted the homing direction of the animal on each trial. Our results demonstrate that the activity of hippocampal neurons with object-anchored firing fields predicts homing behavior.
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spelling pubmed-106518622023-11-15 Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior Najafian Jazi, Maryam Tymorek, Adrian Yen, Ting-Yun Jose Kavarayil, Felix Stingl, Moritz Chau, Sherman Richard Baskurt, Benay García Vilela, Celia Allen, Kevin Nat Commun Article Homing based on path integration (H-PI) is a form of navigation in which an animal uses self-motion cues to keep track of its position and return to a starting point. Despite evidence for a role of the hippocampus in homing behavior, the hippocampal spatial representations associated with H-PI are largely unknown. Here we developed a homing task (AutoPI task) that required a mouse to find a randomly placed lever on an arena before returning to its home base. Recordings from the CA1 area in male mice showed that hippocampal neurons remap between random foraging and AutoPI task, between trials in light and dark conditions, and between search and homing behavior. During the AutoPI task, approximately 25% of the firing fields were anchored to the lever position. The activity of 24% of the cells with a lever-anchored field predicted the homing direction of the animal on each trial. Our results demonstrate that the activity of hippocampal neurons with object-anchored firing fields predicts homing behavior. Nature Publishing Group UK 2023-11-15 /pmc/articles/PMC10651862/ /pubmed/37968268 http://dx.doi.org/10.1038/s41467-023-42642-3 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Najafian Jazi, Maryam
Tymorek, Adrian
Yen, Ting-Yun
Jose Kavarayil, Felix
Stingl, Moritz
Chau, Sherman Richard
Baskurt, Benay
García Vilela, Celia
Allen, Kevin
Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title_full Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title_fullStr Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title_full_unstemmed Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title_short Hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
title_sort hippocampal firing fields anchored to a moving object predict homing direction during path-integration-based behavior
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10651862/
https://www.ncbi.nlm.nih.gov/pubmed/37968268
http://dx.doi.org/10.1038/s41467-023-42642-3
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