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Functional and anatomical specificity in a higher olfactory centre
Most sensory systems are organized into parallel neuronal pathways that process distinct aspects of incoming stimuli. In the insect olfactory system, second order projection neurons target both the mushroom body, required for learning, and the lateral horn (LH), proposed to mediate innate olfactory...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550879/ https://www.ncbi.nlm.nih.gov/pubmed/31112127 http://dx.doi.org/10.7554/eLife.44590 |
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author | Frechter, Shahar Bates, Alexander Shakeel Tootoonian, Sina Dolan, Michael-John Manton, James Jamasb, Arian Rokkum Kohl, Johannes Bock, Davi Jefferis, Gregory |
author_facet | Frechter, Shahar Bates, Alexander Shakeel Tootoonian, Sina Dolan, Michael-John Manton, James Jamasb, Arian Rokkum Kohl, Johannes Bock, Davi Jefferis, Gregory |
author_sort | Frechter, Shahar |
collection | PubMed |
description | Most sensory systems are organized into parallel neuronal pathways that process distinct aspects of incoming stimuli. In the insect olfactory system, second order projection neurons target both the mushroom body, required for learning, and the lateral horn (LH), proposed to mediate innate olfactory behavior. Mushroom body neurons form a sparse olfactory population code, which is not stereotyped across animals. In contrast, odor coding in the LH remains poorly understood. We combine genetic driver lines, anatomical and functional criteria to show that the Drosophila LH has ~1400 neurons and >165 cell types. Genetically labeled LHNs have stereotyped odor responses across animals and on average respond to three times more odors than single projection neurons. LHNs are better odor categorizers than projection neurons, likely due to stereotyped pooling of related inputs. Our results reveal some of the principles by which a higher processing area can extract innate behavioral significance from sensory stimuli. |
format | Online Article Text |
id | pubmed-6550879 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-65508792019-06-12 Functional and anatomical specificity in a higher olfactory centre Frechter, Shahar Bates, Alexander Shakeel Tootoonian, Sina Dolan, Michael-John Manton, James Jamasb, Arian Rokkum Kohl, Johannes Bock, Davi Jefferis, Gregory eLife Neuroscience Most sensory systems are organized into parallel neuronal pathways that process distinct aspects of incoming stimuli. In the insect olfactory system, second order projection neurons target both the mushroom body, required for learning, and the lateral horn (LH), proposed to mediate innate olfactory behavior. Mushroom body neurons form a sparse olfactory population code, which is not stereotyped across animals. In contrast, odor coding in the LH remains poorly understood. We combine genetic driver lines, anatomical and functional criteria to show that the Drosophila LH has ~1400 neurons and >165 cell types. Genetically labeled LHNs have stereotyped odor responses across animals and on average respond to three times more odors than single projection neurons. LHNs are better odor categorizers than projection neurons, likely due to stereotyped pooling of related inputs. Our results reveal some of the principles by which a higher processing area can extract innate behavioral significance from sensory stimuli. eLife Sciences Publications, Ltd 2019-05-21 /pmc/articles/PMC6550879/ /pubmed/31112127 http://dx.doi.org/10.7554/eLife.44590 Text en © 2019, Frechter et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Frechter, Shahar Bates, Alexander Shakeel Tootoonian, Sina Dolan, Michael-John Manton, James Jamasb, Arian Rokkum Kohl, Johannes Bock, Davi Jefferis, Gregory Functional and anatomical specificity in a higher olfactory centre |
title | Functional and anatomical specificity in a higher olfactory centre |
title_full | Functional and anatomical specificity in a higher olfactory centre |
title_fullStr | Functional and anatomical specificity in a higher olfactory centre |
title_full_unstemmed | Functional and anatomical specificity in a higher olfactory centre |
title_short | Functional and anatomical specificity in a higher olfactory centre |
title_sort | functional and anatomical specificity in a higher olfactory centre |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6550879/ https://www.ncbi.nlm.nih.gov/pubmed/31112127 http://dx.doi.org/10.7554/eLife.44590 |
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