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An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen

Lymphoid tissue stromal cells are important regulators of spleen homeostasis and immune responses. Here, we present an optimized protocol that describes the digestion and enrichment steps for the isolation and analysis of rare populations of stromal cells, including fibroblastic reticular cells, per...

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Detalles Bibliográficos
Autores principales: Alexandre, Yannick O., Mueller, Scott N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768415/
https://www.ncbi.nlm.nih.gov/pubmed/36595952
http://dx.doi.org/10.1016/j.xpro.2022.101923
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author Alexandre, Yannick O.
Mueller, Scott N.
author_facet Alexandre, Yannick O.
Mueller, Scott N.
author_sort Alexandre, Yannick O.
collection PubMed
description Lymphoid tissue stromal cells are important regulators of spleen homeostasis and immune responses. Here, we present an optimized protocol that describes the digestion and enrichment steps for the isolation and analysis of rare populations of stromal cells, including fibroblastic reticular cells, perivascular cells, and glial cells found in the spleen. This protocol is suitable for subsequent analysis of spleen stromal cells by flow cytometry or single-cell RNA sequencing and to analyze different disease models. For complete details on the use and execution of this protocol, please refer to Alexandre et al. (2022).(1)
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spelling pubmed-97684152022-12-22 An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen Alexandre, Yannick O. Mueller, Scott N. STAR Protoc Protocol Lymphoid tissue stromal cells are important regulators of spleen homeostasis and immune responses. Here, we present an optimized protocol that describes the digestion and enrichment steps for the isolation and analysis of rare populations of stromal cells, including fibroblastic reticular cells, perivascular cells, and glial cells found in the spleen. This protocol is suitable for subsequent analysis of spleen stromal cells by flow cytometry or single-cell RNA sequencing and to analyze different disease models. For complete details on the use and execution of this protocol, please refer to Alexandre et al. (2022).(1) Elsevier 2022-12-12 /pmc/articles/PMC9768415/ /pubmed/36595952 http://dx.doi.org/10.1016/j.xpro.2022.101923 Text en © 2022 The Author(s) 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
Alexandre, Yannick O.
Mueller, Scott N.
An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title_full An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title_fullStr An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title_full_unstemmed An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title_short An optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
title_sort optimized protocol for the isolation of rare stromal cell populations from the mouse spleen
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768415/
https://www.ncbi.nlm.nih.gov/pubmed/36595952
http://dx.doi.org/10.1016/j.xpro.2022.101923
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