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Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal
The central amygdala (CeA) contains a diverse population of cells, including multiple subtypes of GABAergic neurons, along with glia and epithelial cells. Specific CeA cell types have been shown to affect alcohol consumption in animal models of dependence and may be involved in negative affect durin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300707/ https://www.ncbi.nlm.nih.gov/pubmed/35859068 http://dx.doi.org/10.1038/s41398-022-02063-0 |
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author | Dilly, Geoffrey A. Kittleman, Cory W. Kerr, Tony M. Messing, Robert O. Mayfield, R. Dayne |
author_facet | Dilly, Geoffrey A. Kittleman, Cory W. Kerr, Tony M. Messing, Robert O. Mayfield, R. Dayne |
author_sort | Dilly, Geoffrey A. |
collection | PubMed |
description | The central amygdala (CeA) contains a diverse population of cells, including multiple subtypes of GABAergic neurons, along with glia and epithelial cells. Specific CeA cell types have been shown to affect alcohol consumption in animal models of dependence and may be involved in negative affect during alcohol withdrawal. We used single-nuclei RNA sequencing to determine cell-type specificity of differential gene expression in the CeA induced by alcohol withdrawal. Cells within the CeA were classified using unbiased clustering analyses and identified based on the expression of known marker genes. Differential gene expression analysis was performed on each identified CeA cell-type. It revealed differential gene expression in astrocytes and GABAergic neurons associated with alcohol withdrawal. GABAergic neurons were further subclassified into 13 clusters of cells. Analyzing transcriptomic responses in these subclusters revealed that alcohol exposure induced multiple differentially expressed genes in one subtype of CeA GABAergic neurons, the protein kinase C delta (PKCδ) expressing neurons. These results suggest that PKCδ neurons in the CeA may be uniquely sensitive to the effects of alcohol exposure and identify a novel population of cells in CeA associated with alcohol withdrawal. |
format | Online Article Text |
id | pubmed-9300707 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93007072022-07-22 Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal Dilly, Geoffrey A. Kittleman, Cory W. Kerr, Tony M. Messing, Robert O. Mayfield, R. Dayne Transl Psychiatry Article The central amygdala (CeA) contains a diverse population of cells, including multiple subtypes of GABAergic neurons, along with glia and epithelial cells. Specific CeA cell types have been shown to affect alcohol consumption in animal models of dependence and may be involved in negative affect during alcohol withdrawal. We used single-nuclei RNA sequencing to determine cell-type specificity of differential gene expression in the CeA induced by alcohol withdrawal. Cells within the CeA were classified using unbiased clustering analyses and identified based on the expression of known marker genes. Differential gene expression analysis was performed on each identified CeA cell-type. It revealed differential gene expression in astrocytes and GABAergic neurons associated with alcohol withdrawal. GABAergic neurons were further subclassified into 13 clusters of cells. Analyzing transcriptomic responses in these subclusters revealed that alcohol exposure induced multiple differentially expressed genes in one subtype of CeA GABAergic neurons, the protein kinase C delta (PKCδ) expressing neurons. These results suggest that PKCδ neurons in the CeA may be uniquely sensitive to the effects of alcohol exposure and identify a novel population of cells in CeA associated with alcohol withdrawal. Nature Publishing Group UK 2022-07-20 /pmc/articles/PMC9300707/ /pubmed/35859068 http://dx.doi.org/10.1038/s41398-022-02063-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Dilly, Geoffrey A. Kittleman, Cory W. Kerr, Tony M. Messing, Robert O. Mayfield, R. Dayne Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title | Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title_full | Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title_fullStr | Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title_full_unstemmed | Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title_short | Cell-type specific changes in PKC-delta neurons of the central amygdala during alcohol withdrawal |
title_sort | cell-type specific changes in pkc-delta neurons of the central amygdala during alcohol withdrawal |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9300707/ https://www.ncbi.nlm.nih.gov/pubmed/35859068 http://dx.doi.org/10.1038/s41398-022-02063-0 |
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