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Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting

Muscle stem cells (MuSCs) are the building blocks for regenerating skeletal muscle after trauma. If we intend to maximize the therapeutic potential of MuSCs, we must further study their molecular and functional properties. Here, we present a protocol for the isolation of mouse MuSCs via a two-step e...

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Detalles Bibliográficos
Autores principales: Elizalde, Gabriel, Munoz, Alma Zuniga, Almada, Albert E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618809/
https://www.ncbi.nlm.nih.gov/pubmed/37874680
http://dx.doi.org/10.1016/j.xpro.2023.102656
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author Elizalde, Gabriel
Munoz, Alma Zuniga
Almada, Albert E.
author_facet Elizalde, Gabriel
Munoz, Alma Zuniga
Almada, Albert E.
author_sort Elizalde, Gabriel
collection PubMed
description Muscle stem cells (MuSCs) are the building blocks for regenerating skeletal muscle after trauma. If we intend to maximize the therapeutic potential of MuSCs, we must further study their molecular and functional properties. Here, we present a protocol for the isolation of mouse MuSCs via a two-step enzymatic and mechanical dissociation of skeletal muscle coupled with fluorescence-activated cell sorting (FACS). FACS-isolated MuSCs can be used for various downstream applications including cell culture, cell transduction, immunofluorescence, and gene expression assays. For complete details on the use and execution of this protocol, please refer to Almada et al. (2021).(1)
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spelling pubmed-106188092023-11-02 Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting Elizalde, Gabriel Munoz, Alma Zuniga Almada, Albert E. STAR Protoc Protocol Muscle stem cells (MuSCs) are the building blocks for regenerating skeletal muscle after trauma. If we intend to maximize the therapeutic potential of MuSCs, we must further study their molecular and functional properties. Here, we present a protocol for the isolation of mouse MuSCs via a two-step enzymatic and mechanical dissociation of skeletal muscle coupled with fluorescence-activated cell sorting (FACS). FACS-isolated MuSCs can be used for various downstream applications including cell culture, cell transduction, immunofluorescence, and gene expression assays. For complete details on the use and execution of this protocol, please refer to Almada et al. (2021).(1) Elsevier 2023-10-22 /pmc/articles/PMC10618809/ /pubmed/37874680 http://dx.doi.org/10.1016/j.xpro.2023.102656 Text en © 2023 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
Elizalde, Gabriel
Munoz, Alma Zuniga
Almada, Albert E.
Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title_full Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title_fullStr Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title_full_unstemmed Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title_short Protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
title_sort protocol for the isolation of mouse muscle stem cells using fluorescence-activated cell sorting
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618809/
https://www.ncbi.nlm.nih.gov/pubmed/37874680
http://dx.doi.org/10.1016/j.xpro.2023.102656
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