Co-cultures of Macrophages with Muscle Stem Cells with Fibroadipogenic Precursor Cells from Regenerating Skeletal Muscle.

Cell isolation Co-culture FACS Fibroadipogenic precursors MACS Macrophages Muscle stem cells Skeletal muscle

Journal

Methods in molecular biology (Clifton, N.J.)
ISSN: 1940-6029
Titre abrégé: Methods Mol Biol
Pays: United States
ID NLM: 9214969

Informations de publication

Date de publication:
2023
Historique:
medline: 3 4 2023
entrez: 30 3 2023
pubmed: 31 3 2023
Statut: ppublish

Résumé

Adult muscle stem cells rebuild myofibers after damage. Although they are highly powerful to implement the adult myogenic program, they need environmental cues provided by surrounding cells for efficient and complete regeneration. Muscle stem cell environment includes fibroadipogenic precursors, vascular cells, and macrophages. A way to decipher the complexity of the interactions muscle stem cells establish with their neighborhood is to co-culture cells freshly isolated from the muscle and assess the impact of one cell type on the behavior/fate of the other cell type. Here, we present a protocol allowing the isolation of primary muscle stem cells, macrophages, and fibroadipogenic precursors by Fluorescence Activated Cell Sorting (FACS) or Magnetic Cell Separation (MACS), together with co-culture methods using a specific setup for a short time window to keep as much as possible the in vivo properties of the isolated cells.

Identifiants

pubmed: 36995587
doi: 10.1007/978-1-0716-3036-5_5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

57-71

Informations de copyright

© 2023. Springer Science+Business Media, LLC, part of Springer Nature.

Références

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Auteurs

Georgiana Panci (G)

Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.

Anita E M Kneppers (A)

Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.

Rémi Mounier (R)

Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.

Bénédicte Chazaud (B)

Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France. benedicte.chazaud@inserm.fr.

Gaëtan Juban (G)

Institut NeuroMyoGène, Unité Physiopathologie et Génétique du Neurone et du Muscle, CNRS, UMR5261, INSERM U1315, Université Claude Bernard Lyon 1, Lyon, France.

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