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Novel role for mineralocorticoid receptors in control of a neuronal phenotype

Mineralocorticoid receptors (MRs) in the brain play a role in learning and memory, neuronal differentiation, and regulation of the stress response. Within the hippocampus, the highest expression of MRs is in area CA2. CA2 pyramidal neurons have a distinct molecular makeup resulting in a plasticity-r...

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Autores principales: McCann, Katharine E., Lustberg, Daniel J., Shaughnessy, Emma K., Carstens, Kelly E., Farris, Shannon, Alexander, Georgia M., Radzicki, Daniel, Zhao, Meilan, Dudek, Serena M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234915/
https://www.ncbi.nlm.nih.gov/pubmed/31745235
http://dx.doi.org/10.1038/s41380-019-0598-7
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author McCann, Katharine E.
Lustberg, Daniel J.
Shaughnessy, Emma K.
Carstens, Kelly E.
Farris, Shannon
Alexander, Georgia M.
Radzicki, Daniel
Zhao, Meilan
Dudek, Serena M.
author_facet McCann, Katharine E.
Lustberg, Daniel J.
Shaughnessy, Emma K.
Carstens, Kelly E.
Farris, Shannon
Alexander, Georgia M.
Radzicki, Daniel
Zhao, Meilan
Dudek, Serena M.
author_sort McCann, Katharine E.
collection PubMed
description Mineralocorticoid receptors (MRs) in the brain play a role in learning and memory, neuronal differentiation, and regulation of the stress response. Within the hippocampus, the highest expression of MRs is in area CA2. CA2 pyramidal neurons have a distinct molecular makeup resulting in a plasticity-resistant phenotype, distinguishing them from neurons in CA1 and CA3. Thus, we asked whether MRs regulate CA2 neuron properties and CA2-related behaviors. Using three conditional knockout methods at different stages of development, we found a striking decrease in multiple molecular markers for CA2, an effect mimicked by chronic antagonism of MRs. Furthermore, embryonic deletion of MRs disrupted afferent inputs to CA2 and enabled synaptic potentiation of the normally LTP-resistant synaptic currents in CA2. We also found that CA2-targeted MR knockout was sufficient to disrupt social behavior and alter behavioral responses to novelty. Altogether, these results demonstrate an unappreciated role for MRs in controlling CA2 pyramidal cell identity and in facilitating CA2-dependent behaviors.
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spelling pubmed-72349152021-01-22 Novel role for mineralocorticoid receptors in control of a neuronal phenotype McCann, Katharine E. Lustberg, Daniel J. Shaughnessy, Emma K. Carstens, Kelly E. Farris, Shannon Alexander, Georgia M. Radzicki, Daniel Zhao, Meilan Dudek, Serena M. Mol Psychiatry Article Mineralocorticoid receptors (MRs) in the brain play a role in learning and memory, neuronal differentiation, and regulation of the stress response. Within the hippocampus, the highest expression of MRs is in area CA2. CA2 pyramidal neurons have a distinct molecular makeup resulting in a plasticity-resistant phenotype, distinguishing them from neurons in CA1 and CA3. Thus, we asked whether MRs regulate CA2 neuron properties and CA2-related behaviors. Using three conditional knockout methods at different stages of development, we found a striking decrease in multiple molecular markers for CA2, an effect mimicked by chronic antagonism of MRs. Furthermore, embryonic deletion of MRs disrupted afferent inputs to CA2 and enabled synaptic potentiation of the normally LTP-resistant synaptic currents in CA2. We also found that CA2-targeted MR knockout was sufficient to disrupt social behavior and alter behavioral responses to novelty. Altogether, these results demonstrate an unappreciated role for MRs in controlling CA2 pyramidal cell identity and in facilitating CA2-dependent behaviors. Nature Publishing Group UK 2019-11-19 2021 /pmc/articles/PMC7234915/ /pubmed/31745235 http://dx.doi.org/10.1038/s41380-019-0598-7 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
McCann, Katharine E.
Lustberg, Daniel J.
Shaughnessy, Emma K.
Carstens, Kelly E.
Farris, Shannon
Alexander, Georgia M.
Radzicki, Daniel
Zhao, Meilan
Dudek, Serena M.
Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title_full Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title_fullStr Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title_full_unstemmed Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title_short Novel role for mineralocorticoid receptors in control of a neuronal phenotype
title_sort novel role for mineralocorticoid receptors in control of a neuronal phenotype
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7234915/
https://www.ncbi.nlm.nih.gov/pubmed/31745235
http://dx.doi.org/10.1038/s41380-019-0598-7
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