Cargando…
The neuronal architecture of the mushroom body provides a logic for associative learning
We identified the neurons comprising the Drosophila mushroom body (MB), an associative center in invertebrate brains, and provide a comprehensive map describing their potential connections. Each of the 21 MB output neuron (MBON) types elaborates segregated dendritic arbors along the parallel axons o...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273437/ https://www.ncbi.nlm.nih.gov/pubmed/25535793 http://dx.doi.org/10.7554/eLife.04577 |
_version_ | 1782349833279897600 |
---|---|
author | Aso, Yoshinori Hattori, Daisuke Yu, Yang Johnston, Rebecca M Iyer, Nirmala A Ngo, Teri-TB Dionne, Heather Abbott, LF Axel, Richard Tanimoto, Hiromu Rubin, Gerald M |
author_facet | Aso, Yoshinori Hattori, Daisuke Yu, Yang Johnston, Rebecca M Iyer, Nirmala A Ngo, Teri-TB Dionne, Heather Abbott, LF Axel, Richard Tanimoto, Hiromu Rubin, Gerald M |
author_sort | Aso, Yoshinori |
collection | PubMed |
description | We identified the neurons comprising the Drosophila mushroom body (MB), an associative center in invertebrate brains, and provide a comprehensive map describing their potential connections. Each of the 21 MB output neuron (MBON) types elaborates segregated dendritic arbors along the parallel axons of ∼2000 Kenyon cells, forming 15 compartments that collectively tile the MB lobes. MBON axons project to five discrete neuropils outside of the MB and three MBON types form a feedforward network in the lobes. Each of the 20 dopaminergic neuron (DAN) types projects axons to one, or at most two, of the MBON compartments. Convergence of DAN axons on compartmentalized Kenyon cell–MBON synapses creates a highly ordered unit that can support learning to impose valence on sensory representations. The elucidation of the complement of neurons of the MB provides a comprehensive anatomical substrate from which one can infer a functional logic of associative olfactory learning and memory. DOI: http://dx.doi.org/10.7554/eLife.04577.001 |
format | Online Article Text |
id | pubmed-4273437 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42734372015-01-29 The neuronal architecture of the mushroom body provides a logic for associative learning Aso, Yoshinori Hattori, Daisuke Yu, Yang Johnston, Rebecca M Iyer, Nirmala A Ngo, Teri-TB Dionne, Heather Abbott, LF Axel, Richard Tanimoto, Hiromu Rubin, Gerald M eLife Neuroscience We identified the neurons comprising the Drosophila mushroom body (MB), an associative center in invertebrate brains, and provide a comprehensive map describing their potential connections. Each of the 21 MB output neuron (MBON) types elaborates segregated dendritic arbors along the parallel axons of ∼2000 Kenyon cells, forming 15 compartments that collectively tile the MB lobes. MBON axons project to five discrete neuropils outside of the MB and three MBON types form a feedforward network in the lobes. Each of the 20 dopaminergic neuron (DAN) types projects axons to one, or at most two, of the MBON compartments. Convergence of DAN axons on compartmentalized Kenyon cell–MBON synapses creates a highly ordered unit that can support learning to impose valence on sensory representations. The elucidation of the complement of neurons of the MB provides a comprehensive anatomical substrate from which one can infer a functional logic of associative olfactory learning and memory. DOI: http://dx.doi.org/10.7554/eLife.04577.001 eLife Sciences Publications, Ltd 2014-12-23 /pmc/articles/PMC4273437/ /pubmed/25535793 http://dx.doi.org/10.7554/eLife.04577 Text en © 2014, Aso et al 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 Aso, Yoshinori Hattori, Daisuke Yu, Yang Johnston, Rebecca M Iyer, Nirmala A Ngo, Teri-TB Dionne, Heather Abbott, LF Axel, Richard Tanimoto, Hiromu Rubin, Gerald M The neuronal architecture of the mushroom body provides a logic for associative learning |
title | The neuronal architecture of the mushroom body provides a logic for associative learning |
title_full | The neuronal architecture of the mushroom body provides a logic for associative learning |
title_fullStr | The neuronal architecture of the mushroom body provides a logic for associative learning |
title_full_unstemmed | The neuronal architecture of the mushroom body provides a logic for associative learning |
title_short | The neuronal architecture of the mushroom body provides a logic for associative learning |
title_sort | neuronal architecture of the mushroom body provides a logic for associative learning |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4273437/ https://www.ncbi.nlm.nih.gov/pubmed/25535793 http://dx.doi.org/10.7554/eLife.04577 |
work_keys_str_mv | AT asoyoshinori theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT hattoridaisuke theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT yuyang theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT johnstonrebeccam theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT iyernirmalaa theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT ngoteritb theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT dionneheather theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT abbottlf theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT axelrichard theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT tanimotohiromu theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT rubingeraldm theneuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT asoyoshinori neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT hattoridaisuke neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT yuyang neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT johnstonrebeccam neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT iyernirmalaa neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT ngoteritb neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT dionneheather neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT abbottlf neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT axelrichard neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT tanimotohiromu neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning AT rubingeraldm neuronalarchitectureofthemushroombodyprovidesalogicforassociativelearning |