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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2018
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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. |
format | Online Article Text |
id | pubmed-6089555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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