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Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area
Social stress is a major contributor to neuropsychiatric issues such as depression, substance abuse and eating disorders. The ventral tegmental area (VTA) is involved in the effects of stress on cognitive and emotional processes perturbed in these disorders. However, the VTA is a cellularly heteroge...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304991/ https://www.ncbi.nlm.nih.gov/pubmed/35874648 http://dx.doi.org/10.3389/fnbeh.2022.936087 |
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author | Koutlas, Ioannis Linders, Louisa E. van der Starre, Stef E. Wolterink-Donselaar, Inge G. Adan, Roger A. H. Meye, Frank J. |
author_facet | Koutlas, Ioannis Linders, Louisa E. van der Starre, Stef E. Wolterink-Donselaar, Inge G. Adan, Roger A. H. Meye, Frank J. |
author_sort | Koutlas, Ioannis |
collection | PubMed |
description | Social stress is a major contributor to neuropsychiatric issues such as depression, substance abuse and eating disorders. The ventral tegmental area (VTA) is involved in the effects of stress on cognitive and emotional processes perturbed in these disorders. However, the VTA is a cellularly heterogeneous brain area and it remains unclear which of its neuronal populations make up the social stress-sensitive ensemble. The current study characterizes the molecular, topographical and functional properties of VTA social stress-activated cells. First, we used immunohistochemical analysis of Fos protein, a marker of recent increased neuronal activity, to show that acute social stress activates a mainly neuronal ensemble in the VTA (VTA(Social stress) neurons). Topographical analysis showed that this ensemble, which comprises ∼11% of all VTA neurons, occurs across VTA subregions. Further analysis showed that approximately half of the VTA(Social stress) neurons express the dopamine synthesis rate-limiting enzyme tyrosine hydroxylase (TH). In a minority of cases this occurred with coexpression of vesicular glutamate transporter 2 (Vglut2). Also part of the ensemble were VTA cells expressing just Vglut2 without TH, and cells expressing the vesicular GABA transporter (VGAT) without TH. Next, using targeted recombination in active populations (TRAP2), we showed that VTA(Social stress) neurons can be permanently tagged and made tractable for future functional investigations. Using a combination of TRAP2 and patch-clamp electrophysiology we demonstrate that VTA(Social stress) neurons exhibit higher excitability than their non-TRAPed neighbor cells. Overall, this study shows that acute social stress activates an ensemble of neurons throughout the VTA, comprising distinct molecular identities, and with specific electrophysiological features. It also identifies TRAP2 as a tool to make this ensemble tractable for future functional studies. |
format | Online Article Text |
id | pubmed-9304991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93049912022-07-23 Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area Koutlas, Ioannis Linders, Louisa E. van der Starre, Stef E. Wolterink-Donselaar, Inge G. Adan, Roger A. H. Meye, Frank J. Front Behav Neurosci Neuroscience Social stress is a major contributor to neuropsychiatric issues such as depression, substance abuse and eating disorders. The ventral tegmental area (VTA) is involved in the effects of stress on cognitive and emotional processes perturbed in these disorders. However, the VTA is a cellularly heterogeneous brain area and it remains unclear which of its neuronal populations make up the social stress-sensitive ensemble. The current study characterizes the molecular, topographical and functional properties of VTA social stress-activated cells. First, we used immunohistochemical analysis of Fos protein, a marker of recent increased neuronal activity, to show that acute social stress activates a mainly neuronal ensemble in the VTA (VTA(Social stress) neurons). Topographical analysis showed that this ensemble, which comprises ∼11% of all VTA neurons, occurs across VTA subregions. Further analysis showed that approximately half of the VTA(Social stress) neurons express the dopamine synthesis rate-limiting enzyme tyrosine hydroxylase (TH). In a minority of cases this occurred with coexpression of vesicular glutamate transporter 2 (Vglut2). Also part of the ensemble were VTA cells expressing just Vglut2 without TH, and cells expressing the vesicular GABA transporter (VGAT) without TH. Next, using targeted recombination in active populations (TRAP2), we showed that VTA(Social stress) neurons can be permanently tagged and made tractable for future functional investigations. Using a combination of TRAP2 and patch-clamp electrophysiology we demonstrate that VTA(Social stress) neurons exhibit higher excitability than their non-TRAPed neighbor cells. Overall, this study shows that acute social stress activates an ensemble of neurons throughout the VTA, comprising distinct molecular identities, and with specific electrophysiological features. It also identifies TRAP2 as a tool to make this ensemble tractable for future functional studies. Frontiers Media S.A. 2022-07-08 /pmc/articles/PMC9304991/ /pubmed/35874648 http://dx.doi.org/10.3389/fnbeh.2022.936087 Text en Copyright © 2022 Koutlas, Linders, van der Starre, Wolterink-Donselaar, Adan and Meye. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Koutlas, Ioannis Linders, Louisa E. van der Starre, Stef E. Wolterink-Donselaar, Inge G. Adan, Roger A. H. Meye, Frank J. Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title | Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title_full | Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title_fullStr | Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title_full_unstemmed | Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title_short | Characterizing and TRAPing a Social Stress-Activated Neuronal Ensemble in the Ventral Tegmental Area |
title_sort | characterizing and traping a social stress-activated neuronal ensemble in the ventral tegmental area |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9304991/ https://www.ncbi.nlm.nih.gov/pubmed/35874648 http://dx.doi.org/10.3389/fnbeh.2022.936087 |
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