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A neural circuit linking learning and sleep in Drosophila long-term memory

Animals retain some but not all experiences in long-term memory (LTM). Sleep supports LTM retention across animal species. It is well established that learning experiences enhance post-learning sleep. However, the underlying mechanisms of how learning mediates sleep for memory retention are not clea...

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Autores principales: Lei, Zhengchang, Henderson, Kristin, Keleman, Krystyna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807839/
https://www.ncbi.nlm.nih.gov/pubmed/35105888
http://dx.doi.org/10.1038/s41467-022-28256-1
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author Lei, Zhengchang
Henderson, Kristin
Keleman, Krystyna
author_facet Lei, Zhengchang
Henderson, Kristin
Keleman, Krystyna
author_sort Lei, Zhengchang
collection PubMed
description Animals retain some but not all experiences in long-term memory (LTM). Sleep supports LTM retention across animal species. It is well established that learning experiences enhance post-learning sleep. However, the underlying mechanisms of how learning mediates sleep for memory retention are not clear. Drosophila males display increased amounts of sleep after courtship learning. Courtship learning depends on Mushroom Body (MB) neurons, and post-learning sleep is mediated by the sleep-promoting ventral Fan-Shaped Body neurons (vFBs). We show that post-learning sleep is regulated by two opposing output neurons (MBONs) from the MB, which encode a measure of learning. Excitatory MBONs-γ2α’1 becomes increasingly active upon increasing time of learning, whereas inhibitory MBONs-β’2mp is activated only by a short learning experience. These MB outputs are integrated by SFS neurons, which excite vFBs to promote sleep after prolonged but not short training. This circuit may ensure that only longer or more intense learning experiences induce sleep and are thereby consolidated into LTM.
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spelling pubmed-88078392022-02-07 A neural circuit linking learning and sleep in Drosophila long-term memory Lei, Zhengchang Henderson, Kristin Keleman, Krystyna Nat Commun Article Animals retain some but not all experiences in long-term memory (LTM). Sleep supports LTM retention across animal species. It is well established that learning experiences enhance post-learning sleep. However, the underlying mechanisms of how learning mediates sleep for memory retention are not clear. Drosophila males display increased amounts of sleep after courtship learning. Courtship learning depends on Mushroom Body (MB) neurons, and post-learning sleep is mediated by the sleep-promoting ventral Fan-Shaped Body neurons (vFBs). We show that post-learning sleep is regulated by two opposing output neurons (MBONs) from the MB, which encode a measure of learning. Excitatory MBONs-γ2α’1 becomes increasingly active upon increasing time of learning, whereas inhibitory MBONs-β’2mp is activated only by a short learning experience. These MB outputs are integrated by SFS neurons, which excite vFBs to promote sleep after prolonged but not short training. This circuit may ensure that only longer or more intense learning experiences induce sleep and are thereby consolidated into LTM. Nature Publishing Group UK 2022-02-01 /pmc/articles/PMC8807839/ /pubmed/35105888 http://dx.doi.org/10.1038/s41467-022-28256-1 Text en © The Author(s) 2022 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 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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lei, Zhengchang
Henderson, Kristin
Keleman, Krystyna
A neural circuit linking learning and sleep in Drosophila long-term memory
title A neural circuit linking learning and sleep in Drosophila long-term memory
title_full A neural circuit linking learning and sleep in Drosophila long-term memory
title_fullStr A neural circuit linking learning and sleep in Drosophila long-term memory
title_full_unstemmed A neural circuit linking learning and sleep in Drosophila long-term memory
title_short A neural circuit linking learning and sleep in Drosophila long-term memory
title_sort neural circuit linking learning and sleep in drosophila long-term memory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8807839/
https://www.ncbi.nlm.nih.gov/pubmed/35105888
http://dx.doi.org/10.1038/s41467-022-28256-1
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