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Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli
Priming and activating immune stimuli have profound effects on macrophages, however, studies generally evaluate stimuli in isolation rather than in combination. In this study we have investigated the effects of pro-inflammatory and anti-inflammatory stimuli either alone or in combination on macropha...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851634/ https://www.ncbi.nlm.nih.gov/pubmed/29538444 http://dx.doi.org/10.1371/journal.pone.0194126 |
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author | Rattigan, Kevin M. Pountain, Andrew W. Regnault, Clement Achcar, Fiona Vincent, Isabel M. Goodyear, Carl S. Barrett, Michael P. |
author_facet | Rattigan, Kevin M. Pountain, Andrew W. Regnault, Clement Achcar, Fiona Vincent, Isabel M. Goodyear, Carl S. Barrett, Michael P. |
author_sort | Rattigan, Kevin M. |
collection | PubMed |
description | Priming and activating immune stimuli have profound effects on macrophages, however, studies generally evaluate stimuli in isolation rather than in combination. In this study we have investigated the effects of pro-inflammatory and anti-inflammatory stimuli either alone or in combination on macrophage metabolism. These stimuli include host factors such as IFNγ and ovalbumin-immunoglobulin immune complexes, or pathogen factors such as LPS. Untargeted LC-MS based metabolomics provided an in-depth profile of the macrophage metabolome, and revealed specific changes in metabolite abundance upon either individual stimuli or combined stimuli. Here, by factoring in an interaction term in the linear model, we define the metabolome interactome. This approach allowed us to determine whether stimuli interact in a synergistic or antagonistic manner. In conclusion this study demonstrates a robust approach to interrogate immune-metabolism, especially systems that model host-pathogen interactions. |
format | Online Article Text |
id | pubmed-5851634 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58516342018-03-23 Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli Rattigan, Kevin M. Pountain, Andrew W. Regnault, Clement Achcar, Fiona Vincent, Isabel M. Goodyear, Carl S. Barrett, Michael P. PLoS One Research Article Priming and activating immune stimuli have profound effects on macrophages, however, studies generally evaluate stimuli in isolation rather than in combination. In this study we have investigated the effects of pro-inflammatory and anti-inflammatory stimuli either alone or in combination on macrophage metabolism. These stimuli include host factors such as IFNγ and ovalbumin-immunoglobulin immune complexes, or pathogen factors such as LPS. Untargeted LC-MS based metabolomics provided an in-depth profile of the macrophage metabolome, and revealed specific changes in metabolite abundance upon either individual stimuli or combined stimuli. Here, by factoring in an interaction term in the linear model, we define the metabolome interactome. This approach allowed us to determine whether stimuli interact in a synergistic or antagonistic manner. In conclusion this study demonstrates a robust approach to interrogate immune-metabolism, especially systems that model host-pathogen interactions. Public Library of Science 2018-03-14 /pmc/articles/PMC5851634/ /pubmed/29538444 http://dx.doi.org/10.1371/journal.pone.0194126 Text en © 2018 Rattigan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Rattigan, Kevin M. Pountain, Andrew W. Regnault, Clement Achcar, Fiona Vincent, Isabel M. Goodyear, Carl S. Barrett, Michael P. Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title | Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title_full | Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title_fullStr | Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title_full_unstemmed | Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title_short | Metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
title_sort | metabolomic profiling of macrophages determines the discrete metabolomic signature and metabolomic interactome triggered by polarising immune stimuli |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851634/ https://www.ncbi.nlm.nih.gov/pubmed/29538444 http://dx.doi.org/10.1371/journal.pone.0194126 |
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