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Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila
The behavioral response to a sensory stimulus may depend on both learned and innate neuronal representations. How these circuits interact to produce appropriate behavior is unknown. In Drosophila, the lateral horn (LH) and mushroom body (MB) are thought to mediate innate and learned olfactory behavi...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226615/ https://www.ncbi.nlm.nih.gov/pubmed/30244885 http://dx.doi.org/10.1016/j.neuron.2018.08.037 |
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author | Dolan, Michael-John Belliart-Guérin, Ghislain Bates, Alexander Shakeel Frechter, Shahar Lampin-Saint-Amaux, Aurélie Aso, Yoshinori Roberts, Ruairí J.V. Schlegel, Philipp Wong, Allan Hammad, Adnan Bock, Davi Rubin, Gerald M. Preat, Thomas Plaçais, Pierre-Yves Jefferis, Gregory S.X.E. |
author_facet | Dolan, Michael-John Belliart-Guérin, Ghislain Bates, Alexander Shakeel Frechter, Shahar Lampin-Saint-Amaux, Aurélie Aso, Yoshinori Roberts, Ruairí J.V. Schlegel, Philipp Wong, Allan Hammad, Adnan Bock, Davi Rubin, Gerald M. Preat, Thomas Plaçais, Pierre-Yves Jefferis, Gregory S.X.E. |
author_sort | Dolan, Michael-John |
collection | PubMed |
description | The behavioral response to a sensory stimulus may depend on both learned and innate neuronal representations. How these circuits interact to produce appropriate behavior is unknown. In Drosophila, the lateral horn (LH) and mushroom body (MB) are thought to mediate innate and learned olfactory behavior, respectively, although LH function has not been tested directly. Here we identify two LH cell types (PD2a1 and PD2b1) that receive input from an MB output neuron required for recall of aversive olfactory memories. These neurons are required for aversive memory retrieval and modulated by training. Connectomics data demonstrate that PD2a1 and PD2b1 neurons also receive direct input from food odor-encoding neurons. Consistent with this, PD2a1 and PD2b1 are also necessary for unlearned attraction to some odors, indicating that these neurons have a dual behavioral role. This provides a circuit mechanism by which learned and innate olfactory information can interact in identified neurons to produce appropriate behavior. VIDEO ABSTRACT: |
format | Online Article Text |
id | pubmed-6226615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62266152018-11-16 Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila Dolan, Michael-John Belliart-Guérin, Ghislain Bates, Alexander Shakeel Frechter, Shahar Lampin-Saint-Amaux, Aurélie Aso, Yoshinori Roberts, Ruairí J.V. Schlegel, Philipp Wong, Allan Hammad, Adnan Bock, Davi Rubin, Gerald M. Preat, Thomas Plaçais, Pierre-Yves Jefferis, Gregory S.X.E. Neuron Article The behavioral response to a sensory stimulus may depend on both learned and innate neuronal representations. How these circuits interact to produce appropriate behavior is unknown. In Drosophila, the lateral horn (LH) and mushroom body (MB) are thought to mediate innate and learned olfactory behavior, respectively, although LH function has not been tested directly. Here we identify two LH cell types (PD2a1 and PD2b1) that receive input from an MB output neuron required for recall of aversive olfactory memories. These neurons are required for aversive memory retrieval and modulated by training. Connectomics data demonstrate that PD2a1 and PD2b1 neurons also receive direct input from food odor-encoding neurons. Consistent with this, PD2a1 and PD2b1 are also necessary for unlearned attraction to some odors, indicating that these neurons have a dual behavioral role. This provides a circuit mechanism by which learned and innate olfactory information can interact in identified neurons to produce appropriate behavior. VIDEO ABSTRACT: Cell Press 2018-11-07 /pmc/articles/PMC6226615/ /pubmed/30244885 http://dx.doi.org/10.1016/j.neuron.2018.08.037 Text en © 2018 MRC Laboratory of Molecular Biology http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dolan, Michael-John Belliart-Guérin, Ghislain Bates, Alexander Shakeel Frechter, Shahar Lampin-Saint-Amaux, Aurélie Aso, Yoshinori Roberts, Ruairí J.V. Schlegel, Philipp Wong, Allan Hammad, Adnan Bock, Davi Rubin, Gerald M. Preat, Thomas Plaçais, Pierre-Yves Jefferis, Gregory S.X.E. Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title | Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title_full | Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title_fullStr | Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title_full_unstemmed | Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title_short | Communication from Learned to Innate Olfactory Processing Centers Is Required for Memory Retrieval in Drosophila |
title_sort | communication from learned to innate olfactory processing centers is required for memory retrieval in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6226615/ https://www.ncbi.nlm.nih.gov/pubmed/30244885 http://dx.doi.org/10.1016/j.neuron.2018.08.037 |
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