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Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex

Neuronal plasticity occurs in associative memory. Associative memory cells are recruited for the integration and storage of associated signals. The coordinated refinements and interactions of associative memory cells including glutamatergic and GABAergic neurons remain elusive, which we have examine...

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Autores principales: Feng, Jing, Lu, Wei, Wang, Guang-Yan, Zhu, Zhao-Ming, Sun, Yan, Du, Kaixin, Wang, Jin-Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089555/
https://www.ncbi.nlm.nih.gov/pubmed/30123420
http://dx.doi.org/10.18632/oncotarget.25740
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author Feng, Jing
Lu, Wei
Wang, Guang-Yan
Zhu, Zhao-Ming
Sun, Yan
Du, Kaixin
Wang, Jin-Hui
author_facet Feng, Jing
Lu, Wei
Wang, Guang-Yan
Zhu, Zhao-Ming
Sun, Yan
Du, Kaixin
Wang, Jin-Hui
author_sort Feng, Jing
collection PubMed
description Neuronal plasticity occurs in associative memory. Associative memory cells are recruited for the integration and storage of associated signals. The coordinated refinements and interactions of associative memory cells including glutamatergic and GABAergic neurons remain elusive, which we have examined in a mouse model of associative learning. Paired olfaction, tail and whisker stimulations lead to odorant-induced and tail-induced whisker motions alongside whisker-induced whisker motion. In mice that show this cross-modal associative memory, barrel cortical glutamatergic and GABAergic neurons are recruited to encode the newly learned odor and tail signals alongside the innate whisker signal. These glutamatergic neurons are functionally upregulated, and GABAergic neurons are refined in a homeostatic manner. The mutual innervations between these glutamatergic and GABAergic neurons are upregulated. Therefore, the co-activations of sensory cortices by pairing the input signals recruit their glutamatergic and GABAergic neurons to be associative memory cells, which undergo coordinated refinement among glutamatergic and GABAergic neurons as well as homeostatic plasticity among subcellular compartments in order to drive these cells toward the optimal state for the integrative storage of associated signals.
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spelling pubmed-60895552018-08-17 Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex Feng, Jing Lu, Wei Wang, Guang-Yan Zhu, Zhao-Ming Sun, Yan Du, Kaixin Wang, Jin-Hui Oncotarget Research Paper Neuronal plasticity occurs in associative memory. Associative memory cells are recruited for the integration and storage of associated signals. The coordinated refinements and interactions of associative memory cells including glutamatergic and GABAergic neurons remain elusive, which we have examined in a mouse model of associative learning. Paired olfaction, tail and whisker stimulations lead to odorant-induced and tail-induced whisker motions alongside whisker-induced whisker motion. In mice that show this cross-modal associative memory, barrel cortical glutamatergic and GABAergic neurons are recruited to encode the newly learned odor and tail signals alongside the innate whisker signal. These glutamatergic neurons are functionally upregulated, and GABAergic neurons are refined in a homeostatic manner. The mutual innervations between these glutamatergic and GABAergic neurons are upregulated. Therefore, the co-activations of sensory cortices by pairing the input signals recruit their glutamatergic and GABAergic neurons to be associative memory cells, which undergo coordinated refinement among glutamatergic and GABAergic neurons as well as homeostatic plasticity among subcellular compartments in order to drive these cells toward the optimal state for the integrative storage of associated signals. Impact Journals LLC 2018-07-24 /pmc/articles/PMC6089555/ /pubmed/30123420 http://dx.doi.org/10.18632/oncotarget.25740 Text en Copyright: © 2018 Feng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Feng, Jing
Lu, Wei
Wang, Guang-Yan
Zhu, Zhao-Ming
Sun, Yan
Du, Kaixin
Wang, Jin-Hui
Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title_full Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title_fullStr Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title_full_unstemmed Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title_short Cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
title_sort cell-specific plasticity associated with integrative memory of triple sensory signals in the barrel cortex
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089555/
https://www.ncbi.nlm.nih.gov/pubmed/30123420
http://dx.doi.org/10.18632/oncotarget.25740
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