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Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes

Monocytes are a major population of circulating immune cells that play a crucial role in producing pro-inflammatory cytokines in the body. The actions of monocytes are known to be influenced by the combinations and concentrations of certain fatty acids (FAs) in blood and dietary fats. However, syste...

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Autores principales: Hung, Hao-Chang, Tsai, Sheng-Feng, Chou, Hsuan-Wen, Tsai, Ming-Jun, Hsu, Pei-Ling, Kuo, Yu-Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073224/
https://www.ncbi.nlm.nih.gov/pubmed/37016048
http://dx.doi.org/10.1038/s41598-023-32710-5
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author Hung, Hao-Chang
Tsai, Sheng-Feng
Chou, Hsuan-Wen
Tsai, Ming-Jun
Hsu, Pei-Ling
Kuo, Yu-Min
author_facet Hung, Hao-Chang
Tsai, Sheng-Feng
Chou, Hsuan-Wen
Tsai, Ming-Jun
Hsu, Pei-Ling
Kuo, Yu-Min
author_sort Hung, Hao-Chang
collection PubMed
description Monocytes are a major population of circulating immune cells that play a crucial role in producing pro-inflammatory cytokines in the body. The actions of monocytes are known to be influenced by the combinations and concentrations of certain fatty acids (FAs) in blood and dietary fats. However, systemic comparisons of the effects of FAs on cytokine secretion by monocytes have not be performed. In this study, we compared how six saturated FAs (SFAs), two monounsaturated FAs (MUFAs), and seven polyunsaturated FAs (PUFAs) modulate human THP-1 monocyte secretion of TNF, IL-1β, and IL-6 in the absence or presence of lipopolysaccharide. SFAs generally stimulated resting THP-1 cells to secrete pro-inflammatory cytokines, with stearic acid being the most potent species. In contrast, MUFAs and PUFAs inhibited lipopolysaccharide-induced secretion of pro-inflammatory cytokines. Interestingly, the inhibitory potentials of MUFAs and PUFAs followed U-shaped (TNF and IL-1β) or inverted U-shaped (IL-6) dose–response curves. Among the MUFAs and PUFAs that were analyzed, docosahexaenoic acid (C22:6 n-3) exhibited the largest number of double bonds and was found to be the most potent anti-inflammatory compound. Together, our findings reveal that the chemical compositions and concentrations of dietary FAs are key factors in the intricate regulation of monocyte-mediated inflammation.
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spelling pubmed-100732242023-04-06 Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes Hung, Hao-Chang Tsai, Sheng-Feng Chou, Hsuan-Wen Tsai, Ming-Jun Hsu, Pei-Ling Kuo, Yu-Min Sci Rep Article Monocytes are a major population of circulating immune cells that play a crucial role in producing pro-inflammatory cytokines in the body. The actions of monocytes are known to be influenced by the combinations and concentrations of certain fatty acids (FAs) in blood and dietary fats. However, systemic comparisons of the effects of FAs on cytokine secretion by monocytes have not be performed. In this study, we compared how six saturated FAs (SFAs), two monounsaturated FAs (MUFAs), and seven polyunsaturated FAs (PUFAs) modulate human THP-1 monocyte secretion of TNF, IL-1β, and IL-6 in the absence or presence of lipopolysaccharide. SFAs generally stimulated resting THP-1 cells to secrete pro-inflammatory cytokines, with stearic acid being the most potent species. In contrast, MUFAs and PUFAs inhibited lipopolysaccharide-induced secretion of pro-inflammatory cytokines. Interestingly, the inhibitory potentials of MUFAs and PUFAs followed U-shaped (TNF and IL-1β) or inverted U-shaped (IL-6) dose–response curves. Among the MUFAs and PUFAs that were analyzed, docosahexaenoic acid (C22:6 n-3) exhibited the largest number of double bonds and was found to be the most potent anti-inflammatory compound. Together, our findings reveal that the chemical compositions and concentrations of dietary FAs are key factors in the intricate regulation of monocyte-mediated inflammation. Nature Publishing Group UK 2023-04-04 /pmc/articles/PMC10073224/ /pubmed/37016048 http://dx.doi.org/10.1038/s41598-023-32710-5 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
Hung, Hao-Chang
Tsai, Sheng-Feng
Chou, Hsuan-Wen
Tsai, Ming-Jun
Hsu, Pei-Ling
Kuo, Yu-Min
Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title_full Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title_fullStr Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title_full_unstemmed Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title_short Dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human THP-1 monocytes
title_sort dietary fatty acids differentially affect secretion of pro-inflammatory cytokines in human thp-1 monocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10073224/
https://www.ncbi.nlm.nih.gov/pubmed/37016048
http://dx.doi.org/10.1038/s41598-023-32710-5
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