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Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine
Objectives: Immune responses in migraine are poorly characterized, yet implicated in the disease pathogenesis. This study was carried out to characterize purinergic profiles of T-cells in patients with episodic migraine without aura (MWoA) to provide mechanistic evidence for ATP and adenosine involv...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167492/ https://www.ncbi.nlm.nih.gov/pubmed/30319363 http://dx.doi.org/10.3389/fncel.2018.00326 |
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author | Nurkhametova, Dilyara Kudryavtsev, Igor Khayrutdinova, Olga Serebryakova, Maria Altunbaev, Rashid Malm, Tarja Giniatullin, Rashid |
author_facet | Nurkhametova, Dilyara Kudryavtsev, Igor Khayrutdinova, Olga Serebryakova, Maria Altunbaev, Rashid Malm, Tarja Giniatullin, Rashid |
author_sort | Nurkhametova, Dilyara |
collection | PubMed |
description | Objectives: Immune responses in migraine are poorly characterized, yet implicated in the disease pathogenesis. This study was carried out to characterize purinergic profiles of T-cells in patients with episodic migraine without aura (MWoA) to provide mechanistic evidence for ATP and adenosine involvement in modulation of immune regulation in migraine. Methods: Peripheral blood samples were obtained from patients with migraine (n = 16) and age-matched control subjects (n = 21). Subsets of T-cells were identified by flow cytometry based on specific membrane markers. Results: Migraine patients showed reduced total T-cell counts in the peripheral blood. Whereas the total number of CD3+CD4+, CD3+CD8+, or regulatory T lymphocytes (Treg) was not changed, the proportion of Treg CD45R0+CD62L– and CD45R0–CD62L– cells was increased. Interestingly, in migraine, less Treg cells expressed CD39 and CD73 suggesting disrupted ATP breakdown to adenosine. The negative correlations were observed between the duration of migraine and the relative number of CD73+CD39– Tregs and total number of CD73-positive CD45R0+CD62L+ Tregs. Conclusion: Obtained data indicate that T-cell populations are altered in episodic migraine and suggest the involvement of Tregs in the pathophysiology of this disorder. Reduced expression of CD39 and CD73 suggests promotion of ATP-dependent pro-inflammatory and reduction of adenosine-mediated anti-inflammatory mechanisms in migraine. |
format | Online Article Text |
id | pubmed-6167492 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61674922018-10-12 Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine Nurkhametova, Dilyara Kudryavtsev, Igor Khayrutdinova, Olga Serebryakova, Maria Altunbaev, Rashid Malm, Tarja Giniatullin, Rashid Front Cell Neurosci Cellular Neuroscience Objectives: Immune responses in migraine are poorly characterized, yet implicated in the disease pathogenesis. This study was carried out to characterize purinergic profiles of T-cells in patients with episodic migraine without aura (MWoA) to provide mechanistic evidence for ATP and adenosine involvement in modulation of immune regulation in migraine. Methods: Peripheral blood samples were obtained from patients with migraine (n = 16) and age-matched control subjects (n = 21). Subsets of T-cells were identified by flow cytometry based on specific membrane markers. Results: Migraine patients showed reduced total T-cell counts in the peripheral blood. Whereas the total number of CD3+CD4+, CD3+CD8+, or regulatory T lymphocytes (Treg) was not changed, the proportion of Treg CD45R0+CD62L– and CD45R0–CD62L– cells was increased. Interestingly, in migraine, less Treg cells expressed CD39 and CD73 suggesting disrupted ATP breakdown to adenosine. The negative correlations were observed between the duration of migraine and the relative number of CD73+CD39– Tregs and total number of CD73-positive CD45R0+CD62L+ Tregs. Conclusion: Obtained data indicate that T-cell populations are altered in episodic migraine and suggest the involvement of Tregs in the pathophysiology of this disorder. Reduced expression of CD39 and CD73 suggests promotion of ATP-dependent pro-inflammatory and reduction of adenosine-mediated anti-inflammatory mechanisms in migraine. Frontiers Media S.A. 2018-09-25 /pmc/articles/PMC6167492/ /pubmed/30319363 http://dx.doi.org/10.3389/fncel.2018.00326 Text en Copyright © 2018 Nurkhametova, Kudryavtsev, Khayrutdinova, Serebryakova, Altunbaev, Malm and Giniatullin. http://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 | Cellular Neuroscience Nurkhametova, Dilyara Kudryavtsev, Igor Khayrutdinova, Olga Serebryakova, Maria Altunbaev, Rashid Malm, Tarja Giniatullin, Rashid Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title | Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title_full | Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title_fullStr | Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title_full_unstemmed | Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title_short | Purinergic Profiling of Regulatory T-cells in Patients With Episodic Migraine |
title_sort | purinergic profiling of regulatory t-cells in patients with episodic migraine |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6167492/ https://www.ncbi.nlm.nih.gov/pubmed/30319363 http://dx.doi.org/10.3389/fncel.2018.00326 |
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