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Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation

Trajectory-dependent splitter neurons in the hippocampus encode information about a rodent’s prior trajectory during performance of a continuous alternation task. As such, they provide valuable information for supporting memory-guided behavior. Here, we employed single-photon calcium imaging in free...

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Autores principales: Kinsky, Nathaniel R., Mau, William, Sullivan, David W., Levy, Samuel J., Ruesch, Evan A., Hasselmo, Michael E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229120/
https://www.ncbi.nlm.nih.gov/pubmed/32415083
http://dx.doi.org/10.1038/s41467-020-16226-4
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author Kinsky, Nathaniel R.
Mau, William
Sullivan, David W.
Levy, Samuel J.
Ruesch, Evan A.
Hasselmo, Michael E.
author_facet Kinsky, Nathaniel R.
Mau, William
Sullivan, David W.
Levy, Samuel J.
Ruesch, Evan A.
Hasselmo, Michael E.
author_sort Kinsky, Nathaniel R.
collection PubMed
description Trajectory-dependent splitter neurons in the hippocampus encode information about a rodent’s prior trajectory during performance of a continuous alternation task. As such, they provide valuable information for supporting memory-guided behavior. Here, we employed single-photon calcium imaging in freely moving mice to investigate the emergence and fate of trajectory-dependent activity through learning and mastery of a continuous spatial alternation task. In agreement with others, the quality of trajectory-dependent information in hippocampal neurons correlated with task performance. We thus hypothesized that, due to their utility, splitter neurons would exhibit heightened stability. We find that splitter neurons were more likely to remain active and retained more consistent spatial information across multiple days than other neurons. Furthermore, we find that both splitter neurons and place cells emerged rapidly and maintained stable trajectory-dependent/spatial activity thereafter. Our results suggest that neurons with useful functional coding exhibit heightened stability to support memory guided behavior.
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spelling pubmed-72291202020-06-05 Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation Kinsky, Nathaniel R. Mau, William Sullivan, David W. Levy, Samuel J. Ruesch, Evan A. Hasselmo, Michael E. Nat Commun Article Trajectory-dependent splitter neurons in the hippocampus encode information about a rodent’s prior trajectory during performance of a continuous alternation task. As such, they provide valuable information for supporting memory-guided behavior. Here, we employed single-photon calcium imaging in freely moving mice to investigate the emergence and fate of trajectory-dependent activity through learning and mastery of a continuous spatial alternation task. In agreement with others, the quality of trajectory-dependent information in hippocampal neurons correlated with task performance. We thus hypothesized that, due to their utility, splitter neurons would exhibit heightened stability. We find that splitter neurons were more likely to remain active and retained more consistent spatial information across multiple days than other neurons. Furthermore, we find that both splitter neurons and place cells emerged rapidly and maintained stable trajectory-dependent/spatial activity thereafter. Our results suggest that neurons with useful functional coding exhibit heightened stability to support memory guided behavior. Nature Publishing Group UK 2020-05-15 /pmc/articles/PMC7229120/ /pubmed/32415083 http://dx.doi.org/10.1038/s41467-020-16226-4 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
Kinsky, Nathaniel R.
Mau, William
Sullivan, David W.
Levy, Samuel J.
Ruesch, Evan A.
Hasselmo, Michael E.
Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title_full Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title_fullStr Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title_full_unstemmed Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title_short Trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
title_sort trajectory-modulated hippocampal neurons persist throughout memory-guided navigation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229120/
https://www.ncbi.nlm.nih.gov/pubmed/32415083
http://dx.doi.org/10.1038/s41467-020-16226-4
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