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Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis

Rheumatoid arthritis (RA) is a chronic rheumatic disease with a clear sex-bias. Recent data indicated a role for dopamine in RA pathogenesis, while dopaminergic pathways can be modulated by estrogens. As defined mechanism of action of dopamine on B cell function in RA are unclear, we aimed to elucid...

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Autores principales: Wieber, Karolin, Fleige, Leonie, Tsiami, Styliani, Reinders, Jörg, Braun, Jürgen, Baraliakos, Xenofon, Capellino, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993840/
https://www.ncbi.nlm.nih.gov/pubmed/35396380
http://dx.doi.org/10.1038/s41598-022-09891-6
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author Wieber, Karolin
Fleige, Leonie
Tsiami, Styliani
Reinders, Jörg
Braun, Jürgen
Baraliakos, Xenofon
Capellino, Silvia
author_facet Wieber, Karolin
Fleige, Leonie
Tsiami, Styliani
Reinders, Jörg
Braun, Jürgen
Baraliakos, Xenofon
Capellino, Silvia
author_sort Wieber, Karolin
collection PubMed
description Rheumatoid arthritis (RA) is a chronic rheumatic disease with a clear sex-bias. Recent data indicated a role for dopamine in RA pathogenesis, while dopaminergic pathways can be modulated by estrogens. As defined mechanism of action of dopamine on B cell function in RA are unclear, we aimed to elucidate this, with special focus on sex-differences. Healthy controls (HC, n = 64) and RA patients (n = 61) were recruited. Expression of D(1)–D(5) dopamine receptors (DRs) was investigated by flow cytometry on peripheral blood mononuclear cells (PBMCs). D(1)-like DRs were stimulated in vitro to assess effects on B cell activation and proliferation. Secretion of cytokines and dopamine content were measured by ELISA. All DRs were expressed on PBMCs of HC and RA patients. Dopamine content in PBMCs, and frequency of D(1)DR expressing B cells were significantly higher in RA females (p < 0.001). Expression of D(1)DR on RA B cells correlated positively with disease duration and severity only in women. Combined B cell and D(1)-like DR stimulation induced higher IL-8 and CCL-3 secretion from PBMCs of female RA patients compared to HC. These results indicate sex-specific differences in dopaminergic pathway in RA, with a proinflammatory feature of the D(1)DR pathway in women.
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spelling pubmed-89938402022-04-11 Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis Wieber, Karolin Fleige, Leonie Tsiami, Styliani Reinders, Jörg Braun, Jürgen Baraliakos, Xenofon Capellino, Silvia Sci Rep Article Rheumatoid arthritis (RA) is a chronic rheumatic disease with a clear sex-bias. Recent data indicated a role for dopamine in RA pathogenesis, while dopaminergic pathways can be modulated by estrogens. As defined mechanism of action of dopamine on B cell function in RA are unclear, we aimed to elucidate this, with special focus on sex-differences. Healthy controls (HC, n = 64) and RA patients (n = 61) were recruited. Expression of D(1)–D(5) dopamine receptors (DRs) was investigated by flow cytometry on peripheral blood mononuclear cells (PBMCs). D(1)-like DRs were stimulated in vitro to assess effects on B cell activation and proliferation. Secretion of cytokines and dopamine content were measured by ELISA. All DRs were expressed on PBMCs of HC and RA patients. Dopamine content in PBMCs, and frequency of D(1)DR expressing B cells were significantly higher in RA females (p < 0.001). Expression of D(1)DR on RA B cells correlated positively with disease duration and severity only in women. Combined B cell and D(1)-like DR stimulation induced higher IL-8 and CCL-3 secretion from PBMCs of female RA patients compared to HC. These results indicate sex-specific differences in dopaminergic pathway in RA, with a proinflammatory feature of the D(1)DR pathway in women. Nature Publishing Group UK 2022-04-08 /pmc/articles/PMC8993840/ /pubmed/35396380 http://dx.doi.org/10.1038/s41598-022-09891-6 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 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/) .
spellingShingle Article
Wieber, Karolin
Fleige, Leonie
Tsiami, Styliani
Reinders, Jörg
Braun, Jürgen
Baraliakos, Xenofon
Capellino, Silvia
Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title_full Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title_fullStr Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title_full_unstemmed Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title_short Dopamine receptor 1 expressing B cells exert a proinflammatory role in female patients with rheumatoid arthritis
title_sort dopamine receptor 1 expressing b cells exert a proinflammatory role in female patients with rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8993840/
https://www.ncbi.nlm.nih.gov/pubmed/35396380
http://dx.doi.org/10.1038/s41598-022-09891-6
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