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Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate

Creatine is an organic compound which is utilized in biological activities, especially for adenosine triphosphate (ATP) production in the phosphocreatine system. This is a well-known biochemical reaction that is generally recognized as being mainly driven in specific parts of the body, such as the s...

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Autores principales: SAITO, Suguru, CAO, Duo-Yao, OKUNO, Alato, LI, Xiaomo, PENG, Zhenzi, KELEL, Musin, TSUJI, Noriko M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMFH Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533032/
https://www.ncbi.nlm.nih.gov/pubmed/36258765
http://dx.doi.org/10.12938/bmfh.2022-018
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author SAITO, Suguru
CAO, Duo-Yao
OKUNO, Alato
LI, Xiaomo
PENG, Zhenzi
KELEL, Musin
TSUJI, Noriko M
author_facet SAITO, Suguru
CAO, Duo-Yao
OKUNO, Alato
LI, Xiaomo
PENG, Zhenzi
KELEL, Musin
TSUJI, Noriko M
author_sort SAITO, Suguru
collection PubMed
description Creatine is an organic compound which is utilized in biological activities, especially for adenosine triphosphate (ATP) production in the phosphocreatine system. This is a well-known biochemical reaction that is generally recognized as being mainly driven in specific parts of the body, such as the skeletal muscle and brain. However, our report shows a novel aspect of creatine utilization and ATP synthesis in innate immune cells. Creatine supplementation enhanced immune responses in neutrophils, such as cytokine production, reactive oxygen species (ROS) production, phagocytosis, and NETosis, which were characterized as antibacterial activities. This creatine-induced functional upregulation of neutrophils provided a protective effect in a murine bacterial sepsis model. The mortality rate in mice challenged with Escherichia coli K-12 was decreased by creatine supplementation compared with the control treatment. Corresponding to this decrease in mortality, we found that creatine supplementation decreased blood pro-inflammatory cytokine levels and bacterial colonization in organs. Creatine supplementation significantly increased the cellular ATP level in neutrophils compared with the control treatment. This ATP increase was due to the phosphocreatine system in the creatine-treated neutrophils. In addition, extracellular creatine was used in this ATP synthesis, as inhibition of creatine uptake abolished the increase in ATP in the creatine-treated neutrophils. Thus, creatine is an effective nutrient for modifying the immunological function of neutrophils, which contributes to enhancement of antibacterial immunity.
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spelling pubmed-95330322022-10-17 Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate SAITO, Suguru CAO, Duo-Yao OKUNO, Alato LI, Xiaomo PENG, Zhenzi KELEL, Musin TSUJI, Noriko M Biosci Microbiota Food Health Full Paper Creatine is an organic compound which is utilized in biological activities, especially for adenosine triphosphate (ATP) production in the phosphocreatine system. This is a well-known biochemical reaction that is generally recognized as being mainly driven in specific parts of the body, such as the skeletal muscle and brain. However, our report shows a novel aspect of creatine utilization and ATP synthesis in innate immune cells. Creatine supplementation enhanced immune responses in neutrophils, such as cytokine production, reactive oxygen species (ROS) production, phagocytosis, and NETosis, which were characterized as antibacterial activities. This creatine-induced functional upregulation of neutrophils provided a protective effect in a murine bacterial sepsis model. The mortality rate in mice challenged with Escherichia coli K-12 was decreased by creatine supplementation compared with the control treatment. Corresponding to this decrease in mortality, we found that creatine supplementation decreased blood pro-inflammatory cytokine levels and bacterial colonization in organs. Creatine supplementation significantly increased the cellular ATP level in neutrophils compared with the control treatment. This ATP increase was due to the phosphocreatine system in the creatine-treated neutrophils. In addition, extracellular creatine was used in this ATP synthesis, as inhibition of creatine uptake abolished the increase in ATP in the creatine-treated neutrophils. Thus, creatine is an effective nutrient for modifying the immunological function of neutrophils, which contributes to enhancement of antibacterial immunity. BMFH Press 2022-06-17 2022 /pmc/articles/PMC9533032/ /pubmed/36258765 http://dx.doi.org/10.12938/bmfh.2022-018 Text en ©2022 BMFH Press https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Full Paper
SAITO, Suguru
CAO, Duo-Yao
OKUNO, Alato
LI, Xiaomo
PENG, Zhenzi
KELEL, Musin
TSUJI, Noriko M
Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title_full Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title_fullStr Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title_full_unstemmed Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title_short Creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
title_sort creatine supplementation enhances immunological function of neutrophils by increasing cellular adenosine triphosphate
topic Full Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9533032/
https://www.ncbi.nlm.nih.gov/pubmed/36258765
http://dx.doi.org/10.12938/bmfh.2022-018
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