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Optimized protocol to isolate primary mouse peritoneal macrophage metabolites

Peritoneal macrophages (PMs) have been shown to have higher stability compared to other macrophage subtypes. However, obtaining enough PMs from a single mouse is often a limitation for metabolomics analysis. Here, we describe a protocol to isolate metabolites from a small number of mouse primary PMs...

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Autores principales: De Jesus, Adam, Pusec, Carolina M., Nguyen, Tivoli, Keyhani-Nejad, Farnaz, Gao, Peng, Weinberg, Samuel E., Ardehali, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483642/
https://www.ncbi.nlm.nih.gov/pubmed/36103306
http://dx.doi.org/10.1016/j.xpro.2022.101668
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author De Jesus, Adam
Pusec, Carolina M.
Nguyen, Tivoli
Keyhani-Nejad, Farnaz
Gao, Peng
Weinberg, Samuel E.
Ardehali, Hossein
author_facet De Jesus, Adam
Pusec, Carolina M.
Nguyen, Tivoli
Keyhani-Nejad, Farnaz
Gao, Peng
Weinberg, Samuel E.
Ardehali, Hossein
author_sort De Jesus, Adam
collection PubMed
description Peritoneal macrophages (PMs) have been shown to have higher stability compared to other macrophage subtypes. However, obtaining enough PMs from a single mouse is often a limitation for metabolomics analysis. Here, we describe a protocol to isolate metabolites from a small number of mouse primary PMs for 13C-stable glucose tracing and metabolomics. Our protocol uses X for metabolite extraction instead of methanol. Our protocol can consistently extract metabolites from low cell number samples with fewer steps than methanol-based approaches. For complete details on the use and execution of this protocol, please refer to De Jesus et al., (2022).
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spelling pubmed-94836422022-09-20 Optimized protocol to isolate primary mouse peritoneal macrophage metabolites De Jesus, Adam Pusec, Carolina M. Nguyen, Tivoli Keyhani-Nejad, Farnaz Gao, Peng Weinberg, Samuel E. Ardehali, Hossein STAR Protoc Protocol Peritoneal macrophages (PMs) have been shown to have higher stability compared to other macrophage subtypes. However, obtaining enough PMs from a single mouse is often a limitation for metabolomics analysis. Here, we describe a protocol to isolate metabolites from a small number of mouse primary PMs for 13C-stable glucose tracing and metabolomics. Our protocol uses X for metabolite extraction instead of methanol. Our protocol can consistently extract metabolites from low cell number samples with fewer steps than methanol-based approaches. For complete details on the use and execution of this protocol, please refer to De Jesus et al., (2022). Elsevier 2022-09-13 /pmc/articles/PMC9483642/ /pubmed/36103306 http://dx.doi.org/10.1016/j.xpro.2022.101668 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
De Jesus, Adam
Pusec, Carolina M.
Nguyen, Tivoli
Keyhani-Nejad, Farnaz
Gao, Peng
Weinberg, Samuel E.
Ardehali, Hossein
Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title_full Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title_fullStr Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title_full_unstemmed Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title_short Optimized protocol to isolate primary mouse peritoneal macrophage metabolites
title_sort optimized protocol to isolate primary mouse peritoneal macrophage metabolites
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483642/
https://www.ncbi.nlm.nih.gov/pubmed/36103306
http://dx.doi.org/10.1016/j.xpro.2022.101668
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