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Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit

Sensory information is translated into ensemble representations by various populations of projection neurons in brain circuits. The dynamics of ensemble representations formed by distinct channels of output neurons in diverse behavioral contexts remains largely unknown. We studied the two output neu...

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Autores principales: Yamada, Yoshiyuki, Bhaukaurally, Khaleel, Madarász, Tamás J., Pouget, Alexandre, Rodriguez, Ivan, Carleton, Alan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352733/
https://www.ncbi.nlm.nih.gov/pubmed/28238548
http://dx.doi.org/10.1016/j.neuron.2017.02.006
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author Yamada, Yoshiyuki
Bhaukaurally, Khaleel
Madarász, Tamás J.
Pouget, Alexandre
Rodriguez, Ivan
Carleton, Alan
author_facet Yamada, Yoshiyuki
Bhaukaurally, Khaleel
Madarász, Tamás J.
Pouget, Alexandre
Rodriguez, Ivan
Carleton, Alan
author_sort Yamada, Yoshiyuki
collection PubMed
description Sensory information is translated into ensemble representations by various populations of projection neurons in brain circuits. The dynamics of ensemble representations formed by distinct channels of output neurons in diverse behavioral contexts remains largely unknown. We studied the two output neuron layers in the olfactory bulb (OB), mitral and tufted cells, using chronic two-photon calcium imaging in awake mice. Both output populations displayed similar odor response profiles. During passive sensory experience, both populations showed reorganization of ensemble odor representations yet stable pattern separation across days. Intriguingly, during active odor discrimination learning, mitral but not tufted cells exhibited improved pattern separation, although both populations showed reorganization of ensemble representations. An olfactory circuitry model suggests that cortical feedback on OB interneurons can trigger both forms of plasticity. In conclusion, we show that different OB output layers display unique context-dependent long-term ensemble plasticity, allowing parallel transfer of non-redundant sensory information to downstream centers. VIDEO ABSTRACT:
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spelling pubmed-53527332017-03-24 Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit Yamada, Yoshiyuki Bhaukaurally, Khaleel Madarász, Tamás J. Pouget, Alexandre Rodriguez, Ivan Carleton, Alan Neuron Article Sensory information is translated into ensemble representations by various populations of projection neurons in brain circuits. The dynamics of ensemble representations formed by distinct channels of output neurons in diverse behavioral contexts remains largely unknown. We studied the two output neuron layers in the olfactory bulb (OB), mitral and tufted cells, using chronic two-photon calcium imaging in awake mice. Both output populations displayed similar odor response profiles. During passive sensory experience, both populations showed reorganization of ensemble odor representations yet stable pattern separation across days. Intriguingly, during active odor discrimination learning, mitral but not tufted cells exhibited improved pattern separation, although both populations showed reorganization of ensemble representations. An olfactory circuitry model suggests that cortical feedback on OB interneurons can trigger both forms of plasticity. In conclusion, we show that different OB output layers display unique context-dependent long-term ensemble plasticity, allowing parallel transfer of non-redundant sensory information to downstream centers. VIDEO ABSTRACT: Cell Press 2017-03-08 /pmc/articles/PMC5352733/ /pubmed/28238548 http://dx.doi.org/10.1016/j.neuron.2017.02.006 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Yamada, Yoshiyuki
Bhaukaurally, Khaleel
Madarász, Tamás J.
Pouget, Alexandre
Rodriguez, Ivan
Carleton, Alan
Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title_full Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title_fullStr Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title_full_unstemmed Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title_short Context- and Output Layer-Dependent Long-Term Ensemble Plasticity in a Sensory Circuit
title_sort context- and output layer-dependent long-term ensemble plasticity in a sensory circuit
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5352733/
https://www.ncbi.nlm.nih.gov/pubmed/28238548
http://dx.doi.org/10.1016/j.neuron.2017.02.006
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