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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...

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Autores principales: Yamada, Daichi, Bushey, Daniel, Li, Feng, Hibbard, Karen L, Sammons, Megan, Funke, Jan, Litwin-Kumar, Ashok, Hige, Toshihide, Aso, Yoshinori
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
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.
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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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