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Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients
BACKGROUND: Major depressive disorder (MDD) is related to human’s immune status, and immunological indicators such as mitogen stimulated cell proliferation and cytokines may become candidate biomarkers for disease diagnosis. METHODS: One hundred diagnosed major depressive disorder subjects and 100 h...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186084/ https://www.ncbi.nlm.nih.gov/pubmed/30314474 http://dx.doi.org/10.1186/s12888-018-1906-5 |
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author | Lin, Ping Ding, Bingyu Wu, Yunqiang Dong, Ke Li, Qingtian |
author_facet | Lin, Ping Ding, Bingyu Wu, Yunqiang Dong, Ke Li, Qingtian |
author_sort | Lin, Ping |
collection | PubMed |
description | BACKGROUND: Major depressive disorder (MDD) is related to human’s immune status, and immunological indicators such as mitogen stimulated cell proliferation and cytokines may become candidate biomarkers for disease diagnosis. METHODS: One hundred diagnosed major depressive disorder subjects and 100 health controls were enrolled in this study. Phytohaemagglutinin and lipopolysaccharide stimulated cell proliferations and cytokine concentrations were detected in peripheral blood mononuclear cells from both groups. The corresponding stimulated responses were conducted and confirmed in chronic unpredictable mild stress (CUMS) mice. RESULTS: Compared to the people in control group, there were lower cell proliferations and lower TNF-α produced in lipopolysaccharide stimulated peripheral blood mononuclear cells in depression patients, lower IL-2 and IL-10 produced in phytohaemagglutinin stimulated peripheral blood mononuclear cells in depression patients, higher IL-6, IL-10 and lower IL-2 secretions were detected in peripheral plasma in depression patients. In CUMS mice we found lower splenocyte proliferations, lower IL-1α productions and higher IL-6 secretions in lipopolysaccharide stimulated splenocytes. It seems lipopolysaccharide stimulated cell proliferation activities were inhibited in depressive states. CONCLUSIONS: Lower lipopolysaccharide stimulated cell proliferation and phytohaemagglutinin stimulated or plasma cytokine IL-2 decreases should be potential monitoring indices in the depressive state assessment for major depressive disorder patients. |
format | Online Article Text |
id | pubmed-6186084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61860842018-10-19 Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients Lin, Ping Ding, Bingyu Wu, Yunqiang Dong, Ke Li, Qingtian BMC Psychiatry Research Article BACKGROUND: Major depressive disorder (MDD) is related to human’s immune status, and immunological indicators such as mitogen stimulated cell proliferation and cytokines may become candidate biomarkers for disease diagnosis. METHODS: One hundred diagnosed major depressive disorder subjects and 100 health controls were enrolled in this study. Phytohaemagglutinin and lipopolysaccharide stimulated cell proliferations and cytokine concentrations were detected in peripheral blood mononuclear cells from both groups. The corresponding stimulated responses were conducted and confirmed in chronic unpredictable mild stress (CUMS) mice. RESULTS: Compared to the people in control group, there were lower cell proliferations and lower TNF-α produced in lipopolysaccharide stimulated peripheral blood mononuclear cells in depression patients, lower IL-2 and IL-10 produced in phytohaemagglutinin stimulated peripheral blood mononuclear cells in depression patients, higher IL-6, IL-10 and lower IL-2 secretions were detected in peripheral plasma in depression patients. In CUMS mice we found lower splenocyte proliferations, lower IL-1α productions and higher IL-6 secretions in lipopolysaccharide stimulated splenocytes. It seems lipopolysaccharide stimulated cell proliferation activities were inhibited in depressive states. CONCLUSIONS: Lower lipopolysaccharide stimulated cell proliferation and phytohaemagglutinin stimulated or plasma cytokine IL-2 decreases should be potential monitoring indices in the depressive state assessment for major depressive disorder patients. BioMed Central 2018-10-12 /pmc/articles/PMC6186084/ /pubmed/30314474 http://dx.doi.org/10.1186/s12888-018-1906-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lin, Ping Ding, Bingyu Wu, Yunqiang Dong, Ke Li, Qingtian Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title | Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title_full | Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title_fullStr | Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title_full_unstemmed | Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title_short | Mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
title_sort | mitogen-stimulated cell proliferation and cytokine production in major depressive disorder patients |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6186084/ https://www.ncbi.nlm.nih.gov/pubmed/30314474 http://dx.doi.org/10.1186/s12888-018-1906-5 |
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