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Circuits for integrating learned and innate valences in the insect brain

Animal behavior is shaped both by evolution and by individual experience. Parallel brain pathways encode innate and learned valences of cues, but the way in which they are integrated during action-selection is not well understood. We used electron microscopy to comprehensively map with synaptic reso...

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Autores principales: Eschbach, Claire, Fushiki, Akira, Winding, Michael, Afonso, Bruno, Andrade, Ingrid V, Cocanougher, Benjamin T, Eichler, Katharina, Gepner, Ruben, Si, Guangwei, Valdes-Aleman, Javier, Fetter, Richard D, Gershow, Marc, Jefferis, Gregory SXE, Samuel, Aravinthan DT, Truman, James W, Cardona, Albert, Zlatic, Marta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616581/
https://www.ncbi.nlm.nih.gov/pubmed/34755599
http://dx.doi.org/10.7554/eLife.62567
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author Eschbach, Claire
Fushiki, Akira
Winding, Michael
Afonso, Bruno
Andrade, Ingrid V
Cocanougher, Benjamin T
Eichler, Katharina
Gepner, Ruben
Si, Guangwei
Valdes-Aleman, Javier
Fetter, Richard D
Gershow, Marc
Jefferis, Gregory SXE
Samuel, Aravinthan DT
Truman, James W
Cardona, Albert
Zlatic, Marta
author_facet Eschbach, Claire
Fushiki, Akira
Winding, Michael
Afonso, Bruno
Andrade, Ingrid V
Cocanougher, Benjamin T
Eichler, Katharina
Gepner, Ruben
Si, Guangwei
Valdes-Aleman, Javier
Fetter, Richard D
Gershow, Marc
Jefferis, Gregory SXE
Samuel, Aravinthan DT
Truman, James W
Cardona, Albert
Zlatic, Marta
author_sort Eschbach, Claire
collection PubMed
description Animal behavior is shaped both by evolution and by individual experience. Parallel brain pathways encode innate and learned valences of cues, but the way in which they are integrated during action-selection is not well understood. We used electron microscopy to comprehensively map with synaptic resolution all neurons downstream of all mushroom body (MB) output neurons (encoding learned valences) and characterized their patterns of interaction with lateral horn (LH) neurons (encoding innate valences) in Drosophila larva. The connectome revealed multiple convergence neuron types that receive convergent MB and LH inputs. A subset of these receives excitatory input from positive-valence MB and LH pathways and inhibitory input from negative-valence MB pathways. We confirmed functional connectivity from LH and MB pathways and behavioral roles of two of these neurons. These neurons encode integrated odor value and bidirectionally regulate turning. Based on this, we speculate that learning could potentially skew the balance of excitation and inhibition onto these neurons and thereby modulate turning. Together, our study provides insights into the circuits that integrate learned and innate valences to modify behavior.
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spelling pubmed-86165812021-11-26 Circuits for integrating learned and innate valences in the insect brain Eschbach, Claire Fushiki, Akira Winding, Michael Afonso, Bruno Andrade, Ingrid V Cocanougher, Benjamin T Eichler, Katharina Gepner, Ruben Si, Guangwei Valdes-Aleman, Javier Fetter, Richard D Gershow, Marc Jefferis, Gregory SXE Samuel, Aravinthan DT Truman, James W Cardona, Albert Zlatic, Marta eLife Neuroscience Animal behavior is shaped both by evolution and by individual experience. Parallel brain pathways encode innate and learned valences of cues, but the way in which they are integrated during action-selection is not well understood. We used electron microscopy to comprehensively map with synaptic resolution all neurons downstream of all mushroom body (MB) output neurons (encoding learned valences) and characterized their patterns of interaction with lateral horn (LH) neurons (encoding innate valences) in Drosophila larva. The connectome revealed multiple convergence neuron types that receive convergent MB and LH inputs. A subset of these receives excitatory input from positive-valence MB and LH pathways and inhibitory input from negative-valence MB pathways. We confirmed functional connectivity from LH and MB pathways and behavioral roles of two of these neurons. These neurons encode integrated odor value and bidirectionally regulate turning. Based on this, we speculate that learning could potentially skew the balance of excitation and inhibition onto these neurons and thereby modulate turning. Together, our study provides insights into the circuits that integrate learned and innate valences to modify behavior. eLife Sciences Publications, Ltd 2021-11-10 /pmc/articles/PMC8616581/ /pubmed/34755599 http://dx.doi.org/10.7554/eLife.62567 Text en © 2021, Eschbach 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
Eschbach, Claire
Fushiki, Akira
Winding, Michael
Afonso, Bruno
Andrade, Ingrid V
Cocanougher, Benjamin T
Eichler, Katharina
Gepner, Ruben
Si, Guangwei
Valdes-Aleman, Javier
Fetter, Richard D
Gershow, Marc
Jefferis, Gregory SXE
Samuel, Aravinthan DT
Truman, James W
Cardona, Albert
Zlatic, Marta
Circuits for integrating learned and innate valences in the insect brain
title Circuits for integrating learned and innate valences in the insect brain
title_full Circuits for integrating learned and innate valences in the insect brain
title_fullStr Circuits for integrating learned and innate valences in the insect brain
title_full_unstemmed Circuits for integrating learned and innate valences in the insect brain
title_short Circuits for integrating learned and innate valences in the insect brain
title_sort circuits for integrating learned and innate valences in the insect brain
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8616581/
https://www.ncbi.nlm.nih.gov/pubmed/34755599
http://dx.doi.org/10.7554/eLife.62567
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