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T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients

Serotonin (5-HT) is known as a potent immune cell modulator in autoimmune diseases and should be protective in the pathogenesis of multiple sclerosis (MS). Nevertheless, there is limited knowledge about receptors involved in 5-HT effects as well as induced mechanisms. Among 5-HT receptors, the 5-HT(...

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Autores principales: Reverchon, Flora, Guillard, Colleen, Mollet, Lucile, Auzou, Pascal, Gosset, David, Madouri, Fahima, Valéry, Antoine, Menuet, Arnaud, Ozsancak, Canan, Pallix-Guyot, Maud, Morisset-Lopez, Séverine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599221/
https://www.ncbi.nlm.nih.gov/pubmed/36289679
http://dx.doi.org/10.3390/biomedicines10102418
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author Reverchon, Flora
Guillard, Colleen
Mollet, Lucile
Auzou, Pascal
Gosset, David
Madouri, Fahima
Valéry, Antoine
Menuet, Arnaud
Ozsancak, Canan
Pallix-Guyot, Maud
Morisset-Lopez, Séverine
author_facet Reverchon, Flora
Guillard, Colleen
Mollet, Lucile
Auzou, Pascal
Gosset, David
Madouri, Fahima
Valéry, Antoine
Menuet, Arnaud
Ozsancak, Canan
Pallix-Guyot, Maud
Morisset-Lopez, Séverine
author_sort Reverchon, Flora
collection PubMed
description Serotonin (5-HT) is known as a potent immune cell modulator in autoimmune diseases and should be protective in the pathogenesis of multiple sclerosis (MS). Nevertheless, there is limited knowledge about receptors involved in 5-HT effects as well as induced mechanisms. Among 5-HT receptors, the 5-HT(7) receptor is able to activate naïve T cells and influence the inflammatory response; however, its involvement in the disease has never been studied so far. In this study, we collected blood sample from three groups: acute relapsing MS patients (ARMS), natalizumab-treated MS patients (NTZ), and control subjects. We investigated the 5-HT(7) expression on circulating lymphocytes and evaluated the effects of its activation on cytokine production with peripheral blood mononuclear cell (PBMC) cultures. We found a significant increase in the 5-HT(7) surface expression on T lymphocytes and on the different CD4(+) T cell subsets exclusively in NTZ-treated patients. We also showed that the selective agonist 5-carboxamidotryptamine (5-CT)-induced 5-HT(7)R activation significantly promotes the production of IL-10, a potent immunosuppressive cytokine in PBMCs. This study provides for the first time a dysregulation of 5-HT(7) expression in NTZ-MS patients and its ability to promote IL-10 release, suggesting its protective role. These findings strengthen the evidence that 5-HT(7) may play a role in the immuno-protective mechanisms of NTZ in MS disease and could be considered as an interesting therapeutic target in MS.
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spelling pubmed-95992212022-10-27 T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients Reverchon, Flora Guillard, Colleen Mollet, Lucile Auzou, Pascal Gosset, David Madouri, Fahima Valéry, Antoine Menuet, Arnaud Ozsancak, Canan Pallix-Guyot, Maud Morisset-Lopez, Séverine Biomedicines Article Serotonin (5-HT) is known as a potent immune cell modulator in autoimmune diseases and should be protective in the pathogenesis of multiple sclerosis (MS). Nevertheless, there is limited knowledge about receptors involved in 5-HT effects as well as induced mechanisms. Among 5-HT receptors, the 5-HT(7) receptor is able to activate naïve T cells and influence the inflammatory response; however, its involvement in the disease has never been studied so far. In this study, we collected blood sample from three groups: acute relapsing MS patients (ARMS), natalizumab-treated MS patients (NTZ), and control subjects. We investigated the 5-HT(7) expression on circulating lymphocytes and evaluated the effects of its activation on cytokine production with peripheral blood mononuclear cell (PBMC) cultures. We found a significant increase in the 5-HT(7) surface expression on T lymphocytes and on the different CD4(+) T cell subsets exclusively in NTZ-treated patients. We also showed that the selective agonist 5-carboxamidotryptamine (5-CT)-induced 5-HT(7)R activation significantly promotes the production of IL-10, a potent immunosuppressive cytokine in PBMCs. This study provides for the first time a dysregulation of 5-HT(7) expression in NTZ-MS patients and its ability to promote IL-10 release, suggesting its protective role. These findings strengthen the evidence that 5-HT(7) may play a role in the immuno-protective mechanisms of NTZ in MS disease and could be considered as an interesting therapeutic target in MS. MDPI 2022-09-27 /pmc/articles/PMC9599221/ /pubmed/36289679 http://dx.doi.org/10.3390/biomedicines10102418 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Reverchon, Flora
Guillard, Colleen
Mollet, Lucile
Auzou, Pascal
Gosset, David
Madouri, Fahima
Valéry, Antoine
Menuet, Arnaud
Ozsancak, Canan
Pallix-Guyot, Maud
Morisset-Lopez, Séverine
T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title_full T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title_fullStr T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title_full_unstemmed T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title_short T Lymphocyte Serotonin 5-HT(7) Receptor Is Dysregulated in Natalizumab-Treated Multiple Sclerosis Patients
title_sort t lymphocyte serotonin 5-ht(7) receptor is dysregulated in natalizumab-treated multiple sclerosis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9599221/
https://www.ncbi.nlm.nih.gov/pubmed/36289679
http://dx.doi.org/10.3390/biomedicines10102418
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