Mushroom body efferent neurons responsible for aversive olfactory memory retrieval in Drosophila

This study reports an anatomical and functional screen of mushroom body–extrinsic neurons in Drosophila and finds that MB-V2 cholinergic efferent neurons are essential for retrieval of aversive short- and long-term memory, but not for memory formation or consolidation. During memory retrieval, MB-V2...

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Published inNature neuroscience Vol. 14; no. 7; pp. 903 - 910
Main Authors Tanimoto, Hiromu, Preat, Thomas, Séjourné, Julien, Plaçais, Pierre-Yves, Aso, Yoshinori, Siwanowicz, Igor, Trannoy, Séverine, Thoma, Vladimiros, Tedjakumala, Stevanus R, Rubin, Gerald M, Tchénio, Paul, Ito, Kei, Isabel, Guillaume
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.07.2011
Nature Publishing Group
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Abstract This study reports an anatomical and functional screen of mushroom body–extrinsic neurons in Drosophila and finds that MB-V2 cholinergic efferent neurons are essential for retrieval of aversive short- and long-term memory, but not for memory formation or consolidation. During memory retrieval, MB-V2 neurons reinforce the olfactory pathway involved in innate odor avoidance. Aversive olfactory memory is formed in the mushroom bodies in Drosophila melanogaster . Memory retrieval requires mushroom body output, but the manner in which a memory trace in the mushroom body drives conditioned avoidance of a learned odor remains unknown. To identify neurons that are involved in olfactory memory retrieval, we performed an anatomical and functional screen of defined sets of mushroom body output neurons. We found that MB-V2 neurons were essential for retrieval of both short- and long-lasting memory, but not for memory formation or memory consolidation. MB-V2 neurons are cholinergic efferent neurons that project from the mushroom body vertical lobes to the middle superiormedial protocerebrum and the lateral horn. Notably, the odor response of MB-V2 neurons was modified after conditioning. As the lateral horn has been implicated in innate responses to repellent odorants, we propose that MB-V2 neurons recruit the olfactory pathway involved in innate odor avoidance during memory retrieval.
AbstractList Aversive olfactory memory is formed in the mushroom bodies in Drosophila melanogaster. Memory retrieval requires mushroom body output, but the manner in which a memory trace in the mushroom body drives conditioned avoidance of a learned odor remains unknown. To identify neurons that are involved in olfactory memory retrieval, we performed an anatomical and functional screen of defined sets of mushroom body output neurons. We found that MB-V2 neurons were essential for retrieval of both short- and long-lasting memory, but not for memory formation or memory consolidation. MB-V2 neurons are cholinergic efferent neurons that project from the mushroom body vertical lobes to the middle superiormedial protocerebrum and the lateral horn. Notably, the odor response of MB-V2 neurons was modified after conditioning. As the lateral horn has been implicated in innate responses to repellent odorants, we propose that MB-V2 neurons recruit the olfactory pathway involved in innate odor avoidance during memory retrieval.
Aversive olfactory memory is formed in the Drosophila mushroom bodies (MB). Memory retrieval requires MB output, but it remains unknown how a memory trace in the MB drives conditioned avoidance of a learned odour. To identify neurons involved in olfactory memory retrieval, we performed an anatomical and functional screen of defined sets of MB extrinsic neurons. Here we show that MB-V2 neurons are essential for retrieval of both short- and long-lasting memory, but neither for memory formation nor for memory consolidation. We further show that MB-V2 are cholinergic efferent neurons that project from the MB vertical lobes to the middle superiormedial protocerebrum and the lateral horn (LH). Notably, the odour response of MB-V2 neurons is modified after conditioning. As the LH is implicated in innate responses to repellent odorants, we propose that during memory retrieval, MB-V2 neurons reinforce the olfactory pathway involved in innate odour avoidance.
This study reports an anatomical and functional screen of mushroom body–extrinsic neurons in Drosophila and finds that MB-V2 cholinergic efferent neurons are essential for retrieval of aversive short- and long-term memory, but not for memory formation or consolidation. During memory retrieval, MB-V2 neurons reinforce the olfactory pathway involved in innate odor avoidance. Aversive olfactory memory is formed in the mushroom bodies in Drosophila melanogaster . Memory retrieval requires mushroom body output, but the manner in which a memory trace in the mushroom body drives conditioned avoidance of a learned odor remains unknown. To identify neurons that are involved in olfactory memory retrieval, we performed an anatomical and functional screen of defined sets of mushroom body output neurons. We found that MB-V2 neurons were essential for retrieval of both short- and long-lasting memory, but not for memory formation or memory consolidation. MB-V2 neurons are cholinergic efferent neurons that project from the mushroom body vertical lobes to the middle superiormedial protocerebrum and the lateral horn. Notably, the odor response of MB-V2 neurons was modified after conditioning. As the lateral horn has been implicated in innate responses to repellent odorants, we propose that MB-V2 neurons recruit the olfactory pathway involved in innate odor avoidance during memory retrieval.
Audience Academic
Author Tanimoto, Hiromu
Plaçais, Pierre-Yves
Tchénio, Paul
Preat, Thomas
Séjourné, Julien
Thoma, Vladimiros
Aso, Yoshinori
Ito, Kei
Trannoy, Séverine
Siwanowicz, Igor
Tedjakumala, Stevanus R
Rubin, Gerald M
Isabel, Guillaume
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  givenname: Kei
  surname: Ito
  fullname: Ito, Kei
  organization: Institute of Molecular and Cellular Biosciences, The University of Tokyo, Bunkyo-ku
– sequence: 13
  givenname: Guillaume
  surname: Isabel
  fullname: Isabel, Guillaume
  organization: Genes and Dynamics of Memory Systems, Neurobiology Unit, CNRS, Ecole Supérieure de Physique et de Chimie Industrielles
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ContentType Journal Article
Copyright Springer Nature America, Inc. 2011
COPYRIGHT 2011 Nature Publishing Group
Copyright Nature Publishing Group Jul 2011
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Issue 7
Keywords Learning
Neuroimaging
Animal behaviour
Behaviour
Neurogenetics
Memory
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Snippet This study reports an anatomical and functional screen of mushroom body–extrinsic neurons in Drosophila and finds that MB-V2 cholinergic efferent neurons are...
Aversive olfactory memory is formed in the mushroom bodies in Drosophila melanogaster. Memory retrieval requires mushroom body output, but the manner in which...
Aversive olfactory memory is formed in the Drosophila mushroom bodies (MB). Memory retrieval requires MB output, but it remains unknown how a memory trace in...
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nature
SourceType Open Access Repository
Aggregation Database
Index Database
Publisher
StartPage 903
SubjectTerms 631/378/1697
631/378/2624
Afferent Pathways - physiology
Analysis of Variance
Animal Genetics and Genomics
Animals
Animals, Genetically Modified
Avoidance Learning - physiology
Behavior, Animal
Behavioral Sciences
Biological Techniques
Biomedical and Life Sciences
Biomedicine
CD8 Antigens - metabolism
Choline O-Acetyltransferase - metabolism
Conditioning (Psychology)
Drosophila
Drosophila melanogaster
Drosophila Proteins - genetics
Drosophila Proteins - metabolism
Gene Expression Regulation - physiology
Glutamate Decarboxylase - metabolism
Green Fluorescent Proteins - genetics
Insects
Memory
Memory, Short-Term - physiology
Mental Recall - physiology
Models, Biological
Motor Neurons - classification
Motor Neurons - physiology
Mushroom Bodies - cytology
Mushrooms
Neurobiology
Neurons
Neurosciences
Odorants
Odors
Olfactory Pathways
Physiological aspects
Smell - physiology
Synapsins - metabolism
Temperature
Time Factors
Transcription Factors - metabolism
Tyrosine 3-Monooxygenase - metabolism
Vesicular Glutamate Transport Proteins - metabolism
Title Mushroom body efferent neurons responsible for aversive olfactory memory retrieval in Drosophila
URI http://dx.doi.org/10.1038/nn.2846
https://link.springer.com/article/10.1038/nn.2846
https://www.ncbi.nlm.nih.gov/pubmed/21685917
https://www.proquest.com/docview/896870168
https://search.proquest.com/docview/874186338
https://search.proquest.com/docview/883044032
https://hal.science/hal-00653182
Volume 14
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