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Role of Calcr expressing neurons in the medial amygdala in social contact among females
Social animals become stressed upon social isolation, proactively engaging in affiliative contacts among conspecifics after resocialization. We have previously reported that calcitonin receptor (Calcr) expressing neurons in the central part of the medial preoptic area (cMPOA) mediate contact-seeking...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850531/ https://www.ncbi.nlm.nih.gov/pubmed/36658598 http://dx.doi.org/10.1186/s13041-023-00993-4 |
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author | Fukumitsu, Kansai Huang, Arthur J. McHugh, Thomas J. Kuroda, Kumi O. |
author_facet | Fukumitsu, Kansai Huang, Arthur J. McHugh, Thomas J. Kuroda, Kumi O. |
author_sort | Fukumitsu, Kansai |
collection | PubMed |
description | Social animals become stressed upon social isolation, proactively engaging in affiliative contacts among conspecifics after resocialization. We have previously reported that calcitonin receptor (Calcr) expressing neurons in the central part of the medial preoptic area (cMPOA) mediate contact-seeking behaviors in female mice. Calcr neurons in the posterodorsal part of the medial amygdala (MeApd) are also activated by resocialization, however their role in social affiliation is still unclear. Here we first investigated the functional characteristics of MeApd Calcr + cells; these neurons are GABAergic and show female-biased Calcr expression. Next, using an adeno-associated virus vector expressing a short hairpin RNA targeting Calcr we aimed to identify its molecular role in the MeApd. Inhibiting Calcr expression in the MeApd increased social contacts during resocialization without affecting locomotor activity, suggesting that the endogenous Calcr signaling in the MeApd suppresses social contacts. These results demonstrate the distinct roles of Calcr in the cMPOA and MeApd for regulating social affiliation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-00993-4. |
format | Online Article Text |
id | pubmed-9850531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98505312023-01-20 Role of Calcr expressing neurons in the medial amygdala in social contact among females Fukumitsu, Kansai Huang, Arthur J. McHugh, Thomas J. Kuroda, Kumi O. Mol Brain Short Report Social animals become stressed upon social isolation, proactively engaging in affiliative contacts among conspecifics after resocialization. We have previously reported that calcitonin receptor (Calcr) expressing neurons in the central part of the medial preoptic area (cMPOA) mediate contact-seeking behaviors in female mice. Calcr neurons in the posterodorsal part of the medial amygdala (MeApd) are also activated by resocialization, however their role in social affiliation is still unclear. Here we first investigated the functional characteristics of MeApd Calcr + cells; these neurons are GABAergic and show female-biased Calcr expression. Next, using an adeno-associated virus vector expressing a short hairpin RNA targeting Calcr we aimed to identify its molecular role in the MeApd. Inhibiting Calcr expression in the MeApd increased social contacts during resocialization without affecting locomotor activity, suggesting that the endogenous Calcr signaling in the MeApd suppresses social contacts. These results demonstrate the distinct roles of Calcr in the cMPOA and MeApd for regulating social affiliation. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13041-023-00993-4. BioMed Central 2023-01-19 /pmc/articles/PMC9850531/ /pubmed/36658598 http://dx.doi.org/10.1186/s13041-023-00993-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Short Report Fukumitsu, Kansai Huang, Arthur J. McHugh, Thomas J. Kuroda, Kumi O. Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title | Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title_full | Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title_fullStr | Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title_full_unstemmed | Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title_short | Role of Calcr expressing neurons in the medial amygdala in social contact among females |
title_sort | role of calcr expressing neurons in the medial amygdala in social contact among females |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9850531/ https://www.ncbi.nlm.nih.gov/pubmed/36658598 http://dx.doi.org/10.1186/s13041-023-00993-4 |
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