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The role of TLR2 in exercise-induced immunomodulation in normal weight individuals
Toll-like receptors (TLRs) have been targeted for therapeutic drug development for several disorders, including cardiovascular diseases (CVD), and diabetes mellitus. Daily levels physical activity (PA) has been purported to influence the systemic circulation of cytokines, affecting the overall activ...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318094/ https://www.ncbi.nlm.nih.gov/pubmed/37400578 http://dx.doi.org/10.1038/s41598-023-37811-9 |
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author | Bahman, Fatemah AlSaeed, Halemah Albeloushi, Shaima Al-Mulla, Fahd Ahmad, Rasheed Al-Rashed, Fatema |
author_facet | Bahman, Fatemah AlSaeed, Halemah Albeloushi, Shaima Al-Mulla, Fahd Ahmad, Rasheed Al-Rashed, Fatema |
author_sort | Bahman, Fatemah |
collection | PubMed |
description | Toll-like receptors (TLRs) have been targeted for therapeutic drug development for several disorders, including cardiovascular diseases (CVD), and diabetes mellitus. Daily levels physical activity (PA) has been purported to influence the systemic circulation of cytokines, affecting the overall activation of TLRs and influencing the inflammatory milieu. Objective and self-reported daily PA was tracked in 69 normal-weight adults. Freedson's cut-offs categorized daily PA intensity into the 25th lowest, medium, and top percentiles. Monocytic TLR2 expression was quantified by flow cytometry in fresh whole blood. Cross-sectional associations between flow cytometry measured TLR2(+) subsets and clinical biomarkers were evaluated. PA increased circulation of TLR2(+) monocytes. TLR2 expression was adversely corelated with reduced diastolic blood pressure (DBP), triglyceride (TG), and matrix metallopeptidase 9 (MMP9) levels. However, regression analysis indicated that only TG levels were independently linked with TLR2(+) subsets in circulation in active participants. Higher daily levels of physical activity are associated with improved cardiovascular blood markers and elevated circulatory monocytic TLR2(+) subsets. These findings suggest that TLR2 may play a role in modulating CVD risk factors in individuals leading physically active lifestyles. |
format | Online Article Text |
id | pubmed-10318094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-103180942023-07-05 The role of TLR2 in exercise-induced immunomodulation in normal weight individuals Bahman, Fatemah AlSaeed, Halemah Albeloushi, Shaima Al-Mulla, Fahd Ahmad, Rasheed Al-Rashed, Fatema Sci Rep Article Toll-like receptors (TLRs) have been targeted for therapeutic drug development for several disorders, including cardiovascular diseases (CVD), and diabetes mellitus. Daily levels physical activity (PA) has been purported to influence the systemic circulation of cytokines, affecting the overall activation of TLRs and influencing the inflammatory milieu. Objective and self-reported daily PA was tracked in 69 normal-weight adults. Freedson's cut-offs categorized daily PA intensity into the 25th lowest, medium, and top percentiles. Monocytic TLR2 expression was quantified by flow cytometry in fresh whole blood. Cross-sectional associations between flow cytometry measured TLR2(+) subsets and clinical biomarkers were evaluated. PA increased circulation of TLR2(+) monocytes. TLR2 expression was adversely corelated with reduced diastolic blood pressure (DBP), triglyceride (TG), and matrix metallopeptidase 9 (MMP9) levels. However, regression analysis indicated that only TG levels were independently linked with TLR2(+) subsets in circulation in active participants. Higher daily levels of physical activity are associated with improved cardiovascular blood markers and elevated circulatory monocytic TLR2(+) subsets. These findings suggest that TLR2 may play a role in modulating CVD risk factors in individuals leading physically active lifestyles. Nature Publishing Group UK 2023-07-03 /pmc/articles/PMC10318094/ /pubmed/37400578 http://dx.doi.org/10.1038/s41598-023-37811-9 Text en © The Author(s) 2023 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 Bahman, Fatemah AlSaeed, Halemah Albeloushi, Shaima Al-Mulla, Fahd Ahmad, Rasheed Al-Rashed, Fatema The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title | The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title_full | The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title_fullStr | The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title_full_unstemmed | The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title_short | The role of TLR2 in exercise-induced immunomodulation in normal weight individuals |
title_sort | role of tlr2 in exercise-induced immunomodulation in normal weight individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318094/ https://www.ncbi.nlm.nih.gov/pubmed/37400578 http://dx.doi.org/10.1038/s41598-023-37811-9 |
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