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Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response
Chronic stress is now recognized as a risk factor for disease development and/or exacerbation. It has been shown to affect negatively the immune system and notably the humoral immune response. Corticotropin-releasing hormone (CRH) is known to play a crucial role in stress response. CRH receptors are...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760685/ https://www.ncbi.nlm.nih.gov/pubmed/29317694 http://dx.doi.org/10.1038/s41598-017-18401-y |
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author | Harlé, Guillaume Kaminski, Sandra Dubayle, David Frippiat, Jean-Pol Ropars, Armelle |
author_facet | Harlé, Guillaume Kaminski, Sandra Dubayle, David Frippiat, Jean-Pol Ropars, Armelle |
author_sort | Harlé, Guillaume |
collection | PubMed |
description | Chronic stress is now recognized as a risk factor for disease development and/or exacerbation. It has been shown to affect negatively the immune system and notably the humoral immune response. Corticotropin-releasing hormone (CRH) is known to play a crucial role in stress response. CRH receptors are expressed on different immune cells such as granulocytes, monocytes and T cells. However, up to now, no CRH receptor has been described on B cells which are key players of the humoral immune response. In order to highlight new pathways by which stress may impact immunity, we investigated the role of CRH in B cells. Here we show that splenic B cells express the CRH receptor 2 (CRHR2), but not CRHR1. This receptor is functional since CRH treatment of B cells activates different signaling pathways (e.g. p38) and decreases B cell viability. Finally, we show that immunization of mice with two types of antigens induces a more intense CRHR staining in secondary lymphoid organs where B cells are known to respond to the antigen. Altogether our results demonstrate, for the first time, that CRH is able to modulate directly B cell activity through the presence of CRHR2. |
format | Online Article Text |
id | pubmed-5760685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57606852018-01-17 Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response Harlé, Guillaume Kaminski, Sandra Dubayle, David Frippiat, Jean-Pol Ropars, Armelle Sci Rep Article Chronic stress is now recognized as a risk factor for disease development and/or exacerbation. It has been shown to affect negatively the immune system and notably the humoral immune response. Corticotropin-releasing hormone (CRH) is known to play a crucial role in stress response. CRH receptors are expressed on different immune cells such as granulocytes, monocytes and T cells. However, up to now, no CRH receptor has been described on B cells which are key players of the humoral immune response. In order to highlight new pathways by which stress may impact immunity, we investigated the role of CRH in B cells. Here we show that splenic B cells express the CRH receptor 2 (CRHR2), but not CRHR1. This receptor is functional since CRH treatment of B cells activates different signaling pathways (e.g. p38) and decreases B cell viability. Finally, we show that immunization of mice with two types of antigens induces a more intense CRHR staining in secondary lymphoid organs where B cells are known to respond to the antigen. Altogether our results demonstrate, for the first time, that CRH is able to modulate directly B cell activity through the presence of CRHR2. Nature Publishing Group UK 2018-01-09 /pmc/articles/PMC5760685/ /pubmed/29317694 http://dx.doi.org/10.1038/s41598-017-18401-y Text en © The Author(s) 2017 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 Harlé, Guillaume Kaminski, Sandra Dubayle, David Frippiat, Jean-Pol Ropars, Armelle Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title | Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title_full | Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title_fullStr | Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title_full_unstemmed | Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title_short | Murine splenic B cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
title_sort | murine splenic b cells express corticotropin-releasing hormone receptor 2 that affect their viability during a stress response |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760685/ https://www.ncbi.nlm.nih.gov/pubmed/29317694 http://dx.doi.org/10.1038/s41598-017-18401-y |
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