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The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells

This study aimed to assess the post-effort transcriptional changes of selected genes encoding receptors for chemokines and interleukins in young, physically active men to better understand the immunomodulatory effect of physical activity. The participants, aged 16–21 years, performed physical exerci...

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Autores principales: Nowak, Robert, Trzeciak-Ryczek, Alicja, Ciechanowicz, Andrzej, Brodkiewicz, Andrzej, Urasińska, Elżbieta, Kostrzewa-Nowak, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137071/
https://www.ncbi.nlm.nih.gov/pubmed/37190028
http://dx.doi.org/10.3390/cells12081119
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author Nowak, Robert
Trzeciak-Ryczek, Alicja
Ciechanowicz, Andrzej
Brodkiewicz, Andrzej
Urasińska, Elżbieta
Kostrzewa-Nowak, Dorota
author_facet Nowak, Robert
Trzeciak-Ryczek, Alicja
Ciechanowicz, Andrzej
Brodkiewicz, Andrzej
Urasińska, Elżbieta
Kostrzewa-Nowak, Dorota
author_sort Nowak, Robert
collection PubMed
description This study aimed to assess the post-effort transcriptional changes of selected genes encoding receptors for chemokines and interleukins in young, physically active men to better understand the immunomodulatory effect of physical activity. The participants, aged 16–21 years, performed physical exercise tasks of either a maximal multistage 20 m shuttle-run test (beep test) or a repeated speed ability test. The expression of selected genes encoding receptors for chemokines and interleukins in nucleated peripheral blood cells was determined using RT-qPCR. Aerobic endurance activity was a positive stimulant that induced increased expression of CCR1 and CCR2 genes following lactate recovery, while the maximum expression of CCR5 was found immediately post-effort. The increase in the expression of inflammation-related genes encoding chemokine receptors triggered by aerobic effort strengthens the theory that physical effort induces sterile inflammation. Different profiles of studied chemokine receptor gene expression induced by short-term anaerobic effort suggest that not all types of physical effort activate the same immunological pathways. A significant increase in IL17RA gene expression after the beep test confirmed the hypothesis that cells expressing this receptor, including Th17 lymphocyte subsets, can be involved in the creation of an immune response after endurance efforts.
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spelling pubmed-101370712023-04-28 The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells Nowak, Robert Trzeciak-Ryczek, Alicja Ciechanowicz, Andrzej Brodkiewicz, Andrzej Urasińska, Elżbieta Kostrzewa-Nowak, Dorota Cells Article This study aimed to assess the post-effort transcriptional changes of selected genes encoding receptors for chemokines and interleukins in young, physically active men to better understand the immunomodulatory effect of physical activity. The participants, aged 16–21 years, performed physical exercise tasks of either a maximal multistage 20 m shuttle-run test (beep test) or a repeated speed ability test. The expression of selected genes encoding receptors for chemokines and interleukins in nucleated peripheral blood cells was determined using RT-qPCR. Aerobic endurance activity was a positive stimulant that induced increased expression of CCR1 and CCR2 genes following lactate recovery, while the maximum expression of CCR5 was found immediately post-effort. The increase in the expression of inflammation-related genes encoding chemokine receptors triggered by aerobic effort strengthens the theory that physical effort induces sterile inflammation. Different profiles of studied chemokine receptor gene expression induced by short-term anaerobic effort suggest that not all types of physical effort activate the same immunological pathways. A significant increase in IL17RA gene expression after the beep test confirmed the hypothesis that cells expressing this receptor, including Th17 lymphocyte subsets, can be involved in the creation of an immune response after endurance efforts. MDPI 2023-04-09 /pmc/articles/PMC10137071/ /pubmed/37190028 http://dx.doi.org/10.3390/cells12081119 Text en © 2023 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
Nowak, Robert
Trzeciak-Ryczek, Alicja
Ciechanowicz, Andrzej
Brodkiewicz, Andrzej
Urasińska, Elżbieta
Kostrzewa-Nowak, Dorota
The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title_full The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title_fullStr The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title_full_unstemmed The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title_short The Impact of Different Types of Physical Effort on the Expression of Selected Chemokine and Interleukin Receptor Genes in Peripheral Blood Cells
title_sort impact of different types of physical effort on the expression of selected chemokine and interleukin receptor genes in peripheral blood cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10137071/
https://www.ncbi.nlm.nih.gov/pubmed/37190028
http://dx.doi.org/10.3390/cells12081119
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