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FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior
The cochaperone FKBP51, encoded by the Fkbp5 gene, has been identified as central risk factor for anxiety-related disorders and stress system dysregulation. In the brain, the oval bed nucleus of the stria terminalis (ovBNST) has been implicated in stress-induced anxiety. However, the role of Fkbp5 i...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687485/ https://www.ncbi.nlm.nih.gov/pubmed/34872938 http://dx.doi.org/10.1523/ENEURO.0425-21.2021 |
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author | Engelhardt, Clara Tang, Fiona Elkhateib, Radwa Bordes, Joeri Brix, Lea Maria van Doeselaar, Lotte Häusl, Alexander S. Pöhlmann, Max L. Schraut, Karla Yang, Huanqing Chen, Alon Deussing, Jan M. Schmidt, Mathias V. |
author_facet | Engelhardt, Clara Tang, Fiona Elkhateib, Radwa Bordes, Joeri Brix, Lea Maria van Doeselaar, Lotte Häusl, Alexander S. Pöhlmann, Max L. Schraut, Karla Yang, Huanqing Chen, Alon Deussing, Jan M. Schmidt, Mathias V. |
author_sort | Engelhardt, Clara |
collection | PubMed |
description | The cochaperone FKBP51, encoded by the Fkbp5 gene, has been identified as central risk factor for anxiety-related disorders and stress system dysregulation. In the brain, the oval bed nucleus of the stria terminalis (ovBNST) has been implicated in stress-induced anxiety. However, the role of Fkbp5 in the ovBNST and its impact on anxiety-like behavior have remained unknown. Here, we show in mice that Fkbp5 in the ovBNST is reactive to acute stress and coexpressed with the stress-regulated neuropeptides Tac2 and Crh. Subsequently, results obtained from viral-mediated manipulation indicate that Fkbp5 overexpression (OE) in the ovBNST results in an anxiolytic-like tendency regarding behavior and endocrinology, whereas a Fkbp5 knock-out (KO) exposed a clear anxiogenic phenotype, indicating that native ovBNST expression and regulation is necessary for normal anxiety-related behavior. Notably, our data suggests that a stress-induced increase of Fkbp5 in the ovBNST may in fact have a protective role, leading to a transient decrease in anxiety and suppression of a future stress-induced hypothalamic-pituitary-adrenal (HPA) axis activation. Together, our findings provide a first insight into the previously unknown relationship and effects of Fkbp5 and the ovBNST on anxiety-like behavior and HPA axis functioning. |
format | Online Article Text |
id | pubmed-8687485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Society for Neuroscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-86874852021-12-21 FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior Engelhardt, Clara Tang, Fiona Elkhateib, Radwa Bordes, Joeri Brix, Lea Maria van Doeselaar, Lotte Häusl, Alexander S. Pöhlmann, Max L. Schraut, Karla Yang, Huanqing Chen, Alon Deussing, Jan M. Schmidt, Mathias V. eNeuro Research Article: New Research The cochaperone FKBP51, encoded by the Fkbp5 gene, has been identified as central risk factor for anxiety-related disorders and stress system dysregulation. In the brain, the oval bed nucleus of the stria terminalis (ovBNST) has been implicated in stress-induced anxiety. However, the role of Fkbp5 in the ovBNST and its impact on anxiety-like behavior have remained unknown. Here, we show in mice that Fkbp5 in the ovBNST is reactive to acute stress and coexpressed with the stress-regulated neuropeptides Tac2 and Crh. Subsequently, results obtained from viral-mediated manipulation indicate that Fkbp5 overexpression (OE) in the ovBNST results in an anxiolytic-like tendency regarding behavior and endocrinology, whereas a Fkbp5 knock-out (KO) exposed a clear anxiogenic phenotype, indicating that native ovBNST expression and regulation is necessary for normal anxiety-related behavior. Notably, our data suggests that a stress-induced increase of Fkbp5 in the ovBNST may in fact have a protective role, leading to a transient decrease in anxiety and suppression of a future stress-induced hypothalamic-pituitary-adrenal (HPA) axis activation. Together, our findings provide a first insight into the previously unknown relationship and effects of Fkbp5 and the ovBNST on anxiety-like behavior and HPA axis functioning. Society for Neuroscience 2021-12-17 /pmc/articles/PMC8687485/ /pubmed/34872938 http://dx.doi.org/10.1523/ENEURO.0425-21.2021 Text en Copyright © 2021 Engelhardt et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article: New Research Engelhardt, Clara Tang, Fiona Elkhateib, Radwa Bordes, Joeri Brix, Lea Maria van Doeselaar, Lotte Häusl, Alexander S. Pöhlmann, Max L. Schraut, Karla Yang, Huanqing Chen, Alon Deussing, Jan M. Schmidt, Mathias V. FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title | FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title_full | FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title_fullStr | FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title_full_unstemmed | FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title_short | FKBP51 in the Oval Bed Nucleus of the Stria Terminalis Regulates Anxiety-Like Behavior |
title_sort | fkbp51 in the oval bed nucleus of the stria terminalis regulates anxiety-like behavior |
topic | Research Article: New Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8687485/ https://www.ncbi.nlm.nih.gov/pubmed/34872938 http://dx.doi.org/10.1523/ENEURO.0425-21.2021 |
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