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Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal

BACKGROUND: Monocytes are a heterogenous population of immune cells whose subsets and functions become substantially dysregulated with advanced age. Although much of our current understanding of the age-related changes in monocytes is derived from fasting blood samples, most people are predominately...

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Autores principales: Snodgrass, Ryan G., Jiang, Xiaowen, Stephensen, Charles B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472410/
https://www.ncbi.nlm.nih.gov/pubmed/36104734
http://dx.doi.org/10.1186/s12979-022-00297-6
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author Snodgrass, Ryan G.
Jiang, Xiaowen
Stephensen, Charles B.
author_facet Snodgrass, Ryan G.
Jiang, Xiaowen
Stephensen, Charles B.
author_sort Snodgrass, Ryan G.
collection PubMed
description BACKGROUND: Monocytes are a heterogenous population of immune cells whose subsets and functions become substantially dysregulated with advanced age. Although much of our current understanding of the age-related changes in monocytes is derived from fasting blood samples, most people are predominately in the postprandial state during waking hours. As hormonal, metabolic, and immunological changes in response to the consumption of a meal are manifested in postprandial blood, it’s unclear how age-dependent changes in peripheral monocytes at fasting are impacted by a dietary challenge. OBJECTIVE: We investigated the impact of age and meal consumption on circulating monocyte frequencies and subsets defined as classical (CD14 + CD16-), intermediate (CD14 + CD16 +), or non-classical (CD14dim CD16 +) in a cohort of 349 healthy adult volunteers grouped into categories based on their age: young adults (18–33 y, n = 123), middle adults (34–49 y, n = 115), and older adults (50–66 y, n = 111). RESULTS: Following 12-h fast total monocyte counts inversely correlated with subject age. Older adults had significantly fewer circulating monocytes along with elevated levels of TGs, cholesterol, glucose, IL-6, IL-8, TNF, neopterin, and CCL2 compared with young adults. Circulating monocyte pools in older adults consisted of smaller proportions of classical but larger proportions of intermediate and non-classical monocytes. Proportions of classical monocytes were inversely correlated with plasma TNF, IL-8, and neopterin while intermediate monocytes were positively correlated with plasma IL-6, TNF, and neopterin. Three hours after consuming a fat-containing meal postprandial monocyte counts increased in all age groups. Despite age-dependent differences in monocyte subsets at fasting, consumption of a meal induced similar changes in the proportions of classical and non-classical monocytes across age groups. Within the circulating postprandial monocyte pool, percentages of classical monocytes decreased while non-classical monocytes increased. However no change in precursory intermediate monocytes were detected. Our study confirms that ageing is associated with changes in monocyte frequencies and subsets and shows that consuming a fat-containing meal induces temporal changes in monocyte frequency and subsets independently of subject age. CLINICAL TRIAL: Registered on ClincialTrials.gov (Identifier: NCT02367287) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-022-00297-6.
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spelling pubmed-94724102022-09-15 Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal Snodgrass, Ryan G. Jiang, Xiaowen Stephensen, Charles B. Immun Ageing Research BACKGROUND: Monocytes are a heterogenous population of immune cells whose subsets and functions become substantially dysregulated with advanced age. Although much of our current understanding of the age-related changes in monocytes is derived from fasting blood samples, most people are predominately in the postprandial state during waking hours. As hormonal, metabolic, and immunological changes in response to the consumption of a meal are manifested in postprandial blood, it’s unclear how age-dependent changes in peripheral monocytes at fasting are impacted by a dietary challenge. OBJECTIVE: We investigated the impact of age and meal consumption on circulating monocyte frequencies and subsets defined as classical (CD14 + CD16-), intermediate (CD14 + CD16 +), or non-classical (CD14dim CD16 +) in a cohort of 349 healthy adult volunteers grouped into categories based on their age: young adults (18–33 y, n = 123), middle adults (34–49 y, n = 115), and older adults (50–66 y, n = 111). RESULTS: Following 12-h fast total monocyte counts inversely correlated with subject age. Older adults had significantly fewer circulating monocytes along with elevated levels of TGs, cholesterol, glucose, IL-6, IL-8, TNF, neopterin, and CCL2 compared with young adults. Circulating monocyte pools in older adults consisted of smaller proportions of classical but larger proportions of intermediate and non-classical monocytes. Proportions of classical monocytes were inversely correlated with plasma TNF, IL-8, and neopterin while intermediate monocytes were positively correlated with plasma IL-6, TNF, and neopterin. Three hours after consuming a fat-containing meal postprandial monocyte counts increased in all age groups. Despite age-dependent differences in monocyte subsets at fasting, consumption of a meal induced similar changes in the proportions of classical and non-classical monocytes across age groups. Within the circulating postprandial monocyte pool, percentages of classical monocytes decreased while non-classical monocytes increased. However no change in precursory intermediate monocytes were detected. Our study confirms that ageing is associated with changes in monocyte frequencies and subsets and shows that consuming a fat-containing meal induces temporal changes in monocyte frequency and subsets independently of subject age. CLINICAL TRIAL: Registered on ClincialTrials.gov (Identifier: NCT02367287) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12979-022-00297-6. BioMed Central 2022-09-14 /pmc/articles/PMC9472410/ /pubmed/36104734 http://dx.doi.org/10.1186/s12979-022-00297-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Snodgrass, Ryan G.
Jiang, Xiaowen
Stephensen, Charles B.
Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title_full Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title_fullStr Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title_full_unstemmed Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title_short Monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
title_sort monocyte subsets display age-dependent alterations at fasting and undergo non-age-dependent changes following consumption of a meal
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9472410/
https://www.ncbi.nlm.nih.gov/pubmed/36104734
http://dx.doi.org/10.1186/s12979-022-00297-6
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