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In This Article

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

Summary

The precise identification of fibro-adipogenic progenitor cells (FAPs) and muscle stem cells (MuSCs) is critical to studying their biological function in physiological and pathological conditions. This protocol provides guidelines for the isolation, purification, and culture of FAPs and MuSCs from adult mouse muscles.

Abstract

Fibro-adipogenic progenitor cells (FAPs) are a population of skeletal muscle-resident mesenchymal stromal cells (MSCs) capable of differentiating along fibrogenic, adipogenic, osteogenic, or chondrogenic lineage. Together with muscle stem cells (MuSCs), FAPs play a critical role in muscle homeostasis, repair, and regeneration, while actively maintaining and remodeling the extracellular matrix (ECM). In pathological conditions, such as chronic damage and muscular dystrophies, FAPs undergo aberrant activation and differentiate into collagen-producing fibroblasts and adipocytes, leading to fibrosis and intramuscular fatty infiltration. Thus, FAPs play a dual role in muscle regeneration, either by sustaining MuSC turnover and promoting tissue repair or contributing to fibrotic scar formation and ectopic fat infiltrates, which compromise the integrity and function of the skeletal muscle tissue. A proper purification of FAPs and MuSCs is a prerequisite for understanding the biological role of these cells in physiological as well as in pathological conditions. Here, we describe a standardized method for the simultaneous isolation of FAPs and MuSCs from limb muscles of adult mice using fluorescence-activated cell sorting (FACS). The protocol describes in detail the mechanical and enzymatic dissociation of mononucleated cells from whole limb muscles and injured tibialis anterior (TA) muscles. FAPs and MuSCs are subsequently isolated using a semi-automated cell sorter to obtain pure cell populations. We additionally describe an optimized method for culturing quiescent and activated FAPs and MuSCs, either alone or in coculture conditions.

Introduction

The skeletal muscle is the largest tissue in the body, accounting for ~40% of adult human weight, and is responsible for maintaining posture, generating movement, regulating basal energy metabolism, and body temperature1. Skeletal muscle is a highly dynamic tissue and possesses a remarkable ability to adapt to a variety of stimuli, such as mechanical stress, metabolic alterations, and daily environmental factors. In addition, skeletal muscle regenerates in response to acute injury, leading to complete restoration of its morphology and functions2. Skeletal muscle plasticity mainly relies upon a population of resident musc....

Protocol

All animal experiments performed were conducted in compliance with institutional guidelines approved by the Animal Care and Use Committee (ACUC) of the National Institute of Arthritis, Musculoskeletal, and Skin Diseases (NIAMS). Investigators performing this protocol must adhere to their local animal ethics guidelines.

NOTE: This protocol describes in detail how to isolate FAPs and MuSCs from hind limb and injured tibialis anterior (TA) muscles of adult male and female mice (3-6 months) and pr.......

Representative Results

This protocol allows the isolation of approximately one million FAPs and up to 350,000 MuSCs from uninjured hind limbs of wild-type adult mice (3-6 months), corresponding to a yield of 8% for FAPs and 3% for MuSCs of total events. When sorting cells from damaged TA 7 days post-injury, two to three TA muscles are pooled to obtain up to 300,000 FAPs and 120,000 MuSCs, which correspond to a yield of 11% and 4%, respectively. Post-sort purity values are usually above 95% for FAPs and MuSCs.

The ga.......

Discussion

Establishing efficient and reproducible protocols for the identification and isolation of pure adult stem cell populations is the first and most critical step toward understanding their function. Isolated FAPs and MuSCs can be used to conduct multiomics analysis in transplantation experiments as a potential treatment for muscular diseases or can be genetically modified for disease modeling in stem cell therapy.

The protocol described here provides standardized guidelines for the identificatio.......

Acknowledgements

We would like to thank Tom Cheung (The Hong Kong University of Science & Technology) for advice on MuSC isolation. This work was funded by the NIAMS-IRP through NIH grants AR041126 and AR041164.

....

Materials

NameCompanyCatalog NumberComments
5 mL Polypropylene Round-Bottom TubeFalcon352063
5 mL Polystyrene Round-Bottom Tube with Cell-Strainer CapFalcon352235
20 G BD Needle 1 in. single use, sterileBD Biosciences 305175
anti-Alpha 7 Integrin PE (clone:R2F2) (RatIgG2b)The University of British Columbia53-0010-01
APC anti-mouse CD31 AntibodyBioLegend102510
APC anti-mouse CD45 AntibodyBioLegend103112
BD FACSMelody Cell SorterBD Biosciences 
BD Luer-Lok tip control syringe, 10-mLBD Biosciences 309604
Biotin anti-mouse CD106 AntibodyBioLegend105703
C57BL/6J  mouse (Female and Male)The Jackson Laboratory000664
B6.129S4-Pdgfratm11(EGFP)Sor/J mouseThe Jackson Laboratory007669
Corning BioCoat Collagen I 6-well Clear Flat Bottom TC-treated Multiwell PlateCorning356400
Corning BioCoat Collagen I 12-well Clear Flat Bottom TC-treated Multiwell PlateCorning356500
Corning BioCoat Collagen I 24-well Clear Flat Bottom TC-treated Multiwell PlateCorning356408
DAPI Solution (1 mg/mL)ThermoFisher Scientific62248
Disposable Aspirating Pipets, Polystyrene, SterileVWR414004-265
Donkey anti-Goat IgG (H+L) Highly Cross-Adsorbed Secondary Antibody, Alexa Fluor 488ThermoFisher ScientificA-11055
Falcon 40 µm Cell Strainer, Blue, SterileCorning352340
Falcon 60 mm TC-treated Cell Culture Dish, SterileCorning353002
Falcon Centrifuge Tubes, Polypropylene, Sterile, Corning, 15-mLVWR352196
Falcon Centrifuge Tubes, Polypropylene, Sterile, Corning, 50-mLCorning352070
Falcon Round-Bottom Tubes, Polypropylene, CorningVWR60819-728
Falcon Round-Bottom Tubes, Polystyrene, with 35um Cell Strainer Cap CorningVWR21008-948
Fibroblast Growth Factor, Basic, Human, Recombinant (rhFGF, Basic)PromegaG5071
FlowJo 10.8.1
Gibco Collagenase, Type II, powderThermoFisher Scientific17101015
Gibco Dispase, powderThermoFisher Scientific17105041
Gibco DMEM, high glucose, HEPESThermoFisher Scientific12430054
Gibco Fetal Bovine Serum, certified, United StatesThermoFisher Scientific16000044
Gibco Ham's F-10 Nutrient MixThermoFisher Scientific11550043
Gibco Horse Serum, New Zealand originThermoFisher Scientific16050122
Gibco PBS, pH 7.4ThermoFisher Scientific10010023
Gibco PBS (10x), pH 7.4ThermoFisher Scientific70011044
Gibco Penicillin-Streptomycin-Glutamine (100x)ThermoFisher Scientific10378016
Goat anti-Mouse IgG1 cross-absorbed secondary antibody, Alexa Fluor 555ThermoFisher ScientificA-21127
Hardened Fine ScissorsFine Science Tools Inc14090-09
Invitrogen 7-AAD (7-Aminoactinomycin D)ThermoFisher ScientificA1310
Mouse PDGF R alpha AntibodyR&D SystemsAF1062
Normal Donkey SerumFisher ScientificNC9624464
Normal Goat SerumThermoFisher Scientific31872
Pacific Blue anti-mouse Ly-6A/E (Sca 1) AntibodyBioLegend108120
Paraformaldehyde, 16%Fisher ScientificNCC0528893
Pax7 mono-clonal mouse antibody (IgG1) (supernatant)Developmental Study Hybridoma BankN/A
PE/Cyanine7 StreptavidinBioLegend405206
Student Vannas Spring ScissorsFine Science Tools Inc91500-09
Student Dumont #5 ForcepsFine Science Tools Inc91150-20
Triton X-100Sigma-AldrichT8787

References

  1. Baskin, K. K., Winders, B. R., Olson, E. N. Muscle as a "mediator" of systemic metabolism. Cell Metabolism. 21 (2), 237-248 (2015).
  2. Dumont, N. A., Bentzinger, C. F., Sincennes, M. C., Rudnicki, M. A. Satellite cells and skeletal muscle regene....

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