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Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection

Tissue-resident macrophage populations constitute a mosaic of phenotypes, yet how their metabolic states link to the range of phenotypes and functions in vivo is still poorly defined. Here, using high-dimensional spectral flow cytometry, we observe distinct metabolic profiles between different organ...

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Autores principales: Heieis, Graham A., Patente, Thiago A., Almeida, Luís, Vrieling, Frank, Tak, Tamar, Perona-Wright, Georgia, Maizels, Rick M., Stienstra, Rinke, Everts, Bart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497597/
https://www.ncbi.nlm.nih.gov/pubmed/37699869
http://dx.doi.org/10.1038/s41467-023-41353-z
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author Heieis, Graham A.
Patente, Thiago A.
Almeida, Luís
Vrieling, Frank
Tak, Tamar
Perona-Wright, Georgia
Maizels, Rick M.
Stienstra, Rinke
Everts, Bart
author_facet Heieis, Graham A.
Patente, Thiago A.
Almeida, Luís
Vrieling, Frank
Tak, Tamar
Perona-Wright, Georgia
Maizels, Rick M.
Stienstra, Rinke
Everts, Bart
author_sort Heieis, Graham A.
collection PubMed
description Tissue-resident macrophage populations constitute a mosaic of phenotypes, yet how their metabolic states link to the range of phenotypes and functions in vivo is still poorly defined. Here, using high-dimensional spectral flow cytometry, we observe distinct metabolic profiles between different organs and functionally link acetyl CoA carboxylase activity to efferocytotic capacity. Additionally, differences in metabolism are evident within populations from a specific site, corresponding to relative stages of macrophage maturity. Immune perturbation with intestinal helminth infection increases alternative activation and metabolic rewiring of monocyte-derived macrophage populations, while resident TIM4(+) intestinal macrophages remain immunologically and metabolically hyporesponsive. Similar metabolic signatures in alternatively-activated macrophages are seen from different tissues using additional helminth models, but to different magnitudes, indicating further tissue-specific contributions to metabolic states. Thus, our high-dimensional, flow-based metabolic analyses indicates complex metabolic heterogeneity and dynamics of tissue-resident macrophage populations at homeostasis and during helminth infection.
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spelling pubmed-104975972023-09-14 Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection Heieis, Graham A. Patente, Thiago A. Almeida, Luís Vrieling, Frank Tak, Tamar Perona-Wright, Georgia Maizels, Rick M. Stienstra, Rinke Everts, Bart Nat Commun Article Tissue-resident macrophage populations constitute a mosaic of phenotypes, yet how their metabolic states link to the range of phenotypes and functions in vivo is still poorly defined. Here, using high-dimensional spectral flow cytometry, we observe distinct metabolic profiles between different organs and functionally link acetyl CoA carboxylase activity to efferocytotic capacity. Additionally, differences in metabolism are evident within populations from a specific site, corresponding to relative stages of macrophage maturity. Immune perturbation with intestinal helminth infection increases alternative activation and metabolic rewiring of monocyte-derived macrophage populations, while resident TIM4(+) intestinal macrophages remain immunologically and metabolically hyporesponsive. Similar metabolic signatures in alternatively-activated macrophages are seen from different tissues using additional helminth models, but to different magnitudes, indicating further tissue-specific contributions to metabolic states. Thus, our high-dimensional, flow-based metabolic analyses indicates complex metabolic heterogeneity and dynamics of tissue-resident macrophage populations at homeostasis and during helminth infection. Nature Publishing Group UK 2023-09-12 /pmc/articles/PMC10497597/ /pubmed/37699869 http://dx.doi.org/10.1038/s41467-023-41353-z 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
Heieis, Graham A.
Patente, Thiago A.
Almeida, Luís
Vrieling, Frank
Tak, Tamar
Perona-Wright, Georgia
Maizels, Rick M.
Stienstra, Rinke
Everts, Bart
Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title_full Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title_fullStr Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title_full_unstemmed Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title_short Metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
title_sort metabolic heterogeneity of tissue-resident macrophages in homeostasis and during helminth infection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10497597/
https://www.ncbi.nlm.nih.gov/pubmed/37699869
http://dx.doi.org/10.1038/s41467-023-41353-z
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