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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

Skeletal muscle comprises multiple cell types, including resident stem cells, each with a special contribution to muscle homeostasis and regeneration. Here, the 2D culture of muscle stem cells and the muscle cell niche in an ex vivo setting that preserves many of the physiological, in vivo, and environmental characteristics are described.

Abstract

Skeletal muscle is the largest tissue of the body and performs multiple functions, from locomotion to body temperature control. Its functionality and recovery from injuries depend on a multitude of cell types and on molecular signals between the core muscle cells (myofibers, muscle stem cells) and their niche. Most experimental settings do not preserve this complex physiological microenvironment, and neither do they allow the ex vivo study of muscle stem cells in quiescence, a cell state that is crucial for them. Here, a protocol is outlined for the ex vivo culture of muscle stem cells with cellular components of their niche. Through the mechanical and enzymatic breakdown of muscles, a mixture of cell types is obtained, which is put in 2D culture. Immunostaining shows that within 1 week, multiple niche cells are present in culture alongside myofibers and, importantly, Pax7-positive cells that display the characteristics of quiescent muscle stem cells. These unique properties make this protocol a powerful tool for cell amplification and the generation of quiescent-like stem cells that can be used to address fundamental and translational questions.

Introduction

Movement, breathing, metabolism, body posture, and body temperature maintenance all depend on skeletal muscle, and malfunctions in the skeletal muscle can, thus, cause debilitating pathologies (i.e., myopathies, muscular dystrophies, etc.)1. Given its essential functions and abundance, skeletal muscle has drawn the attention of research labs worldwide that strive to understand the key aspects that support normal muscle function and can serve as therapeutic targets. In addition, skeletal muscle is a widely used model to study regeneration and stem cell function, as healthy muscle can fully self-repair after complete injury ....

Protocol

All experiments complied with French and EU animal regulations at the Institut Mondor de Recherche Biomédicale (INSERM U955), notably the directive 2010/63/UE. Animals were kept in a controlled and enriched environment at the animal facilities with certification numbers A94 028 379 and D94-028-028; they were handled only by authorized researchers and animal caretakers, and they were visually inspected by animal housing personnel for signs of discomfort during their lifetime. They were euthanized by cervical dis.......

Representative Results

This protocol allows for muscle cell culture while preserving the satellite cells and most cells from their endogenous niche. Figure 2 summarizes the main steps of the protocol, while essential parts of the dissection and digestion are presented in Figure 1. Dissection of the hindlimb musculature is recommended (Figure 1A-C), as this group of muscles is well studied and shares a developmental origin.......

Discussion

Adult skeletal muscle function is underpinned by a finely orchestrated set of cellular interactions and molecular signals. Here, a method is presented that allows for the study of these parameters in an ex vivo setting that closely resembles the physiological microenvironment.

Several groups have reported in vitro methods to culture myogenic cells. These methods aimed to isolate satellite cells to study their myogenic progenitor properties. Two main approaches are used to iso.......

Acknowledgements

For Figure 2, templates from Servier Medical Art (https://smart.servier.com/) were used. The FR lab is supported by the Association Française contre les Myopathies - AFM via TRANSLAMUSCLE (grants 19507 and 22946), the Fondation pour la Recherche Médicale - FRM (EQU202003010217, ENV202004011730, ECO201806006793), the Agence Nationale pour la Recherche - ANR (ANR-21-CE13-0006-02, ANR-19-CE13-0010, ANR-10-LABX-73), and the La Ligue Contre le Cancer (IP/SC-17130). The above funders had no role in the design, collection, analysis, interpretation, or reporting of this study or the writing of this manuscript.

....

Materials

NameCompanyCatalog NumberComments
anti-CD31BD550274dilution 1:100
anti-FOSBSanta Cruzsc-7203dilution 1:200
anti-GFPAbcamab13970dilution 1:1000
anti-Ki67Abcamab16667dilution 1:1000
anti-MyHCDSHBMF20-cdilution 1:400
anti-MYODActive Motif39991dilution 1:200
anti-MYOGSanta Cruzsc-576dilution 1:150
anti-Pax7Santa Cruzsc-81648dilution 1:100
anti-PDGFRαInvitrogenPA5-16571dilution 1:50
b-FGFPeprotech450-33concentration 4 ng/mL
bovine serum albumin (BSA) – used for digestion Sigma AldrichA7906-1006concentration 0.2%
BSA IgG-free, protease-free – used for stainingJackson ImmunoResearch001-000-162concentration 5%
cell strainer 40 umDominique Dutscher352340
cell strainer 70 umDominique Dutscher352350
cell strainer 100 umDominique Dutscher352360
CollagenaseRoche10103586001concentration 0.5 U/mL
Dimethyl sulfoxide (DMSO)EuromedexUD8050-05-A
DispaseRoche4942078001concentration 3 U/mL
Dissection forceps size 5Fine Science Tools91150-20
Dissection forceps size 55Fine Science Tools11295-51
Dissection scissors (big, straight)Fine Science Tools9146-11ideal for chopping
Dissection scissors (small, curved)Fine Science Tools15017-10
Dissection scissors (small, straight)Fine Science Tools14084-08
Dulbecco's Modified Eagle's Medium (DMEM)ThermoFisher41966-029
EdU Click-iT kitThermoFisherC10340
Fetal bovine serum – option 1EurobioCVF00-01
Fetal bovine serum – option 2Gibco10270-106 
MatrigelCorning Life Sciences354234coating solution
ParafilmDominique Dutscher090261flexible film
Penicillin streptomycinGibco15140-122
Paraformaldehyde – option 1PanReac AppliChem ITW Reagents211511.1209concentration 4%
Paraformaldeyde – option 2ThermoFisher28908concentration 4%
Shaking water bathThermoFisherTSSWB27
TritonX100Sigma AldrichT8532-500 MLconcentration 0.5%
Wild-type miceJanvierC57BL/6NRj

References

  1. Frontera, W. R., Ochala, J. Skeletal muscle: A brief review of structure and function. Calcified Tissue International. 96 (3), 183-195 (2015).
  2. Forcina, L., Cosentino, M., Musarò, A.

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