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Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward

During goal-directed navigation, “what” information, which describes the experiences occurring in periods surrounding a reward, can be combined with spatial “where” information to guide behavior and form episodic memories(1,2). This integrative process is thought to occur in the hippocampus(3), whic...

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Autores principales: Issa, John B., Radvansky, Brad A., Xuan, Feng, Dombeck, Daniel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592707/
https://www.ncbi.nlm.nih.gov/pubmed/37873482
http://dx.doi.org/10.1101/2023.10.09.561557
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author Issa, John B.
Radvansky, Brad A.
Xuan, Feng
Dombeck, Daniel A.
author_facet Issa, John B.
Radvansky, Brad A.
Xuan, Feng
Dombeck, Daniel A.
author_sort Issa, John B.
collection PubMed
description During goal-directed navigation, “what” information, which describes the experiences occurring in periods surrounding a reward, can be combined with spatial “where” information to guide behavior and form episodic memories(1,2). This integrative process is thought to occur in the hippocampus(3), which receives spatial information from the medial entorhinal cortex (MEC)(4); however, the source of the “what” information and how it is represented is largely unknown. Here, by establishing a novel imaging method, we show that the lateral entorhinal cortex (LEC) of mice represents key experiential epochs during a reward-based navigation task. We discover a population of neurons that signals goal approach and a separate population of neurons that signals goal departure. A third population of neurons signals reward consumption. When reward location is moved, these populations immediately shift their respective representations of each experiential epoch relative to reward, while optogenetic inhibition of LEC disrupts learning of the new reward location. Together, these results indicate the LEC provides a stable code of experiential epochs surrounding and including reward consumption, providing reward-centric information to contextualize the spatial information carried by the MEC. Such parallel representations are well-suited for generating episodic memories of rewarding experiences and guiding flexible and efficient goal-directed navigation(5-7).
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spelling pubmed-105927072023-10-24 Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward Issa, John B. Radvansky, Brad A. Xuan, Feng Dombeck, Daniel A. bioRxiv Article During goal-directed navigation, “what” information, which describes the experiences occurring in periods surrounding a reward, can be combined with spatial “where” information to guide behavior and form episodic memories(1,2). This integrative process is thought to occur in the hippocampus(3), which receives spatial information from the medial entorhinal cortex (MEC)(4); however, the source of the “what” information and how it is represented is largely unknown. Here, by establishing a novel imaging method, we show that the lateral entorhinal cortex (LEC) of mice represents key experiential epochs during a reward-based navigation task. We discover a population of neurons that signals goal approach and a separate population of neurons that signals goal departure. A third population of neurons signals reward consumption. When reward location is moved, these populations immediately shift their respective representations of each experiential epoch relative to reward, while optogenetic inhibition of LEC disrupts learning of the new reward location. Together, these results indicate the LEC provides a stable code of experiential epochs surrounding and including reward consumption, providing reward-centric information to contextualize the spatial information carried by the MEC. Such parallel representations are well-suited for generating episodic memories of rewarding experiences and guiding flexible and efficient goal-directed navigation(5-7). Cold Spring Harbor Laboratory 2023-10-10 /pmc/articles/PMC10592707/ /pubmed/37873482 http://dx.doi.org/10.1101/2023.10.09.561557 Text en https://creativecommons.org/licenses/by-nd/4.0/This work is licensed under a Creative Commons Attribution-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, and only so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Issa, John B.
Radvansky, Brad A.
Xuan, Feng
Dombeck, Daniel A.
Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title_full Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title_fullStr Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title_full_unstemmed Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title_short Lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
title_sort lateral entorhinal cortex subpopulations represent experiential epochs surrounding reward
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592707/
https://www.ncbi.nlm.nih.gov/pubmed/37873482
http://dx.doi.org/10.1101/2023.10.09.561557
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