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Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila
Dopaminergic neurons with distinct projection patterns and physiological properties compose memory subsystems in a brain. However, it is poorly understood whether or how they interact during complex learning. Here, we identify a feedforward circuit formed between dopamine subsystems and show that it...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937650/ https://www.ncbi.nlm.nih.gov/pubmed/36692262 http://dx.doi.org/10.7554/eLife.79042 |
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author | Yamada, Daichi Bushey, Daniel Li, Feng Hibbard, Karen L Sammons, Megan Funke, Jan Litwin-Kumar, Ashok Hige, Toshihide Aso, Yoshinori |
author_facet | Yamada, Daichi Bushey, Daniel Li, Feng Hibbard, Karen L Sammons, Megan Funke, Jan Litwin-Kumar, Ashok Hige, Toshihide Aso, Yoshinori |
author_sort | Yamada, Daichi |
collection | PubMed |
description | Dopaminergic neurons with distinct projection patterns and physiological properties compose memory subsystems in a brain. However, it is poorly understood whether or how they interact during complex learning. Here, we identify a feedforward circuit formed between dopamine subsystems and show that it is essential for second-order conditioning, an ethologically important form of higher-order associative learning. The Drosophila mushroom body comprises a series of dopaminergic compartments, each of which exhibits distinct memory dynamics. We find that a slow and stable memory compartment can serve as an effective ‘teacher’ by instructing other faster and transient memory compartments via a single key interneuron, which we identify by connectome analysis and neurotransmitter prediction. This excitatory interneuron acquires enhanced response to reward-predicting odor after first-order conditioning and, upon activation, evokes dopamine release in the ‘student’ compartments. These hierarchical connections between dopamine subsystems explain distinct properties of first- and second-order memory long known by behavioral psychologists. |
format | Online Article Text |
id | pubmed-9937650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-99376502023-02-18 Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila Yamada, Daichi Bushey, Daniel Li, Feng Hibbard, Karen L Sammons, Megan Funke, Jan Litwin-Kumar, Ashok Hige, Toshihide Aso, Yoshinori eLife Neuroscience Dopaminergic neurons with distinct projection patterns and physiological properties compose memory subsystems in a brain. However, it is poorly understood whether or how they interact during complex learning. Here, we identify a feedforward circuit formed between dopamine subsystems and show that it is essential for second-order conditioning, an ethologically important form of higher-order associative learning. The Drosophila mushroom body comprises a series of dopaminergic compartments, each of which exhibits distinct memory dynamics. We find that a slow and stable memory compartment can serve as an effective ‘teacher’ by instructing other faster and transient memory compartments via a single key interneuron, which we identify by connectome analysis and neurotransmitter prediction. This excitatory interneuron acquires enhanced response to reward-predicting odor after first-order conditioning and, upon activation, evokes dopamine release in the ‘student’ compartments. These hierarchical connections between dopamine subsystems explain distinct properties of first- and second-order memory long known by behavioral psychologists. eLife Sciences Publications, Ltd 2023-01-24 /pmc/articles/PMC9937650/ /pubmed/36692262 http://dx.doi.org/10.7554/eLife.79042 Text en © 2023, Yamada 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 Yamada, Daichi Bushey, Daniel Li, Feng Hibbard, Karen L Sammons, Megan Funke, Jan Litwin-Kumar, Ashok Hige, Toshihide Aso, Yoshinori Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title | Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title_full | Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title_fullStr | Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title_full_unstemmed | Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title_short | Hierarchical architecture of dopaminergic circuits enables second-order conditioning in Drosophila |
title_sort | hierarchical architecture of dopaminergic circuits enables second-order conditioning in drosophila |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9937650/ https://www.ncbi.nlm.nih.gov/pubmed/36692262 http://dx.doi.org/10.7554/eLife.79042 |
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