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Recurrent architecture for adaptive regulation of learning in the insect brain
Dopaminergic neurons (DANs) drive learning across the animal kingdom, but the upstream circuits that regulate their activity and thereby learning remain poorly understood. We provide the first synaptic-resolution connectome of the circuitry upstream of all DANs in a learning center, the mush-room bo...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145459/ https://www.ncbi.nlm.nih.gov/pubmed/32203499 http://dx.doi.org/10.1038/s41593-020-0607-9 |
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author | Eschbach, Claire Fushiki, Akira Winding, Michael Schneider-Mizell, Casey M. Shao, Mei Arruda, Rebecca Eichler, Katharina Valdes-Aleman, Javier Ohyama, Tomoko Thum, Andreas S. Gerber, Bertram Fetter, Richard D. Truman, James W. Litwin-Kumar, Ashok Cardona, Albert Zlatic, Marta |
author_facet | Eschbach, Claire Fushiki, Akira Winding, Michael Schneider-Mizell, Casey M. Shao, Mei Arruda, Rebecca Eichler, Katharina Valdes-Aleman, Javier Ohyama, Tomoko Thum, Andreas S. Gerber, Bertram Fetter, Richard D. Truman, James W. Litwin-Kumar, Ashok Cardona, Albert Zlatic, Marta |
author_sort | Eschbach, Claire |
collection | PubMed |
description | Dopaminergic neurons (DANs) drive learning across the animal kingdom, but the upstream circuits that regulate their activity and thereby learning remain poorly understood. We provide the first synaptic-resolution connectome of the circuitry upstream of all DANs in a learning center, the mush-room body (MB) of Drosophila larva. We discover afferent sensory pathways and a large population of neurons that provide feedback from MB output neurons and link distinct memory systems (aversive and appetitive). We combine this with functional studies of DANs and their presynaptic partners and with comprehensive circuit modelling. We find that DANs compare convergent feedback from aversive and appetitive systems which enables the computation of integrated predictions that may improve future learning. Computational modelling reveals that the discovered feedback motifs increase model flexibility and performance on learning tasks. Our study provides the most detailed view to date of biological circuit motifs that support associative learning. |
format | Online Article Text |
id | pubmed-7145459 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
record_format | MEDLINE/PubMed |
spelling | pubmed-71454592020-09-23 Recurrent architecture for adaptive regulation of learning in the insect brain Eschbach, Claire Fushiki, Akira Winding, Michael Schneider-Mizell, Casey M. Shao, Mei Arruda, Rebecca Eichler, Katharina Valdes-Aleman, Javier Ohyama, Tomoko Thum, Andreas S. Gerber, Bertram Fetter, Richard D. Truman, James W. Litwin-Kumar, Ashok Cardona, Albert Zlatic, Marta Nat Neurosci Article Dopaminergic neurons (DANs) drive learning across the animal kingdom, but the upstream circuits that regulate their activity and thereby learning remain poorly understood. We provide the first synaptic-resolution connectome of the circuitry upstream of all DANs in a learning center, the mush-room body (MB) of Drosophila larva. We discover afferent sensory pathways and a large population of neurons that provide feedback from MB output neurons and link distinct memory systems (aversive and appetitive). We combine this with functional studies of DANs and their presynaptic partners and with comprehensive circuit modelling. We find that DANs compare convergent feedback from aversive and appetitive systems which enables the computation of integrated predictions that may improve future learning. Computational modelling reveals that the discovered feedback motifs increase model flexibility and performance on learning tasks. Our study provides the most detailed view to date of biological circuit motifs that support associative learning. 2020-03-23 2020-04 /pmc/articles/PMC7145459/ /pubmed/32203499 http://dx.doi.org/10.1038/s41593-020-0607-9 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Eschbach, Claire Fushiki, Akira Winding, Michael Schneider-Mizell, Casey M. Shao, Mei Arruda, Rebecca Eichler, Katharina Valdes-Aleman, Javier Ohyama, Tomoko Thum, Andreas S. Gerber, Bertram Fetter, Richard D. Truman, James W. Litwin-Kumar, Ashok Cardona, Albert Zlatic, Marta Recurrent architecture for adaptive regulation of learning in the insect brain |
title | Recurrent architecture for adaptive regulation of learning in the insect brain |
title_full | Recurrent architecture for adaptive regulation of learning in the insect brain |
title_fullStr | Recurrent architecture for adaptive regulation of learning in the insect brain |
title_full_unstemmed | Recurrent architecture for adaptive regulation of learning in the insect brain |
title_short | Recurrent architecture for adaptive regulation of learning in the insect brain |
title_sort | recurrent architecture for adaptive regulation of learning in the insect brain |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7145459/ https://www.ncbi.nlm.nih.gov/pubmed/32203499 http://dx.doi.org/10.1038/s41593-020-0607-9 |
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