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In This Article

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

Summary

This protocol outlines a method to isolate Fibro-adipogenic progenitors (FAPs) and myogenic progenitors (MPs) from rat skeletal muscle. Utilization of the rat in muscle injury models provides increased tissue availability from atrophic muscle for the analysis and a larger repertoire of validated methods to assess muscle strength and gait in free-moving animals.

Abstract

Fibro-adipogenic Progenitors (FAPs) are resident interstitial cells in skeletal muscle that, together with myogenic progenitors (MPs), play a key role in muscle homeostasis, injury, and repair. Current protocols for FAPs identification and isolation use flow cytometry/fluorescence-activated cell sorting (FACS) and studies evaluating their function in vivo to date have been undertaken exclusively in mice. The larger inherent size of the rat allows for a more comprehensive analysis of FAPs in skeletal muscle injury models, especially in severely atrophic muscle or when investigators require substantial tissue mass to conduct multiple downstream assays. The rat additionally provides a larger selection of muscle functional assays that do not require animal sedation or sacrifice, thus minimizing morbidity and animal use by enabling serial assessments. The flow cytometry/FACS protocols optimized for mice are species specific, notably restricted by the characteristics of commercially available antibodies. They have not been optimized for separating FAPs from rat or highly fibrotic muscle. A flow cytometry/FACS protocol for the identification and isolation of FAPs and MPs from both healthy and denervated rat skeletal muscle was developed, relying on the differential expression of surface markers CD31, CD45, Sca-1, and VCAM-1. As rat-specific, flow cytometry-validated primary antibodies are severely limited, in-house conjugation of the antibody targeting Sca-1 was performed. Using this protocol, successful Sca-1 conjugation was confirmed, and flow cytometric identification of FAPs and MPs was validated by cell culture and immunostaining of FACS-isolated FAPs and MPs. Finally, we report a novel FAPs time-course in a prolonged (14 week) rat denervation model. This method provides the investigators the ability to study FAPs in a novel animal model.

Introduction

Fibro-adipogenic progenitor cells (FAPs) are a population of resident multipotent progenitor cells in skeletal muscle that play a critical role in muscle homeostasis, repair, and regeneration, and conversely, also mediate pathologic responses to muscle injury. As the name suggests, FAPs were originally identified as a progenitor population with the potential to differentiate into fibroblasts and adipocytes1 and were purported to be the key mediators of fibro-fatty infiltration of skeletal muscle in chronic injury and disease. Further study revealed that FAPs are additionally capable of osteogenesis and chondrogenesis2

Protocol

Investigators conducting this protocol must receive permission from their local animal ethics board/care committee. All animal work was approved by the St. Michael's Hospital Unity Health Toronto Animal Care Committee (ACC #918) and was conducted in accordance with the guidelines set forth by the Canadian Council on Animal Care (CCAC). A schematic of the flow cytometry protocol is shown in Figure 1. If the downstream application is FACS and subsequent cell culture, all steps should be co.......

Representative Results

Identifying FAPs and MPs via flow cytometry using a novel antibody panel including Sca-1 and VCAM-1
The gating strategy for identifying FAPs in rat muscle is based upon flow cytometry protocols in the mouse29, which gate on CD31 (endothelial) and CD45 (hematopoietic) positive cells (termed the lineage [Lin]) and examines the fluorescent profile of FAPs marker Sca-1 and MPs marker ITGA7 from the linage-negative (Lin-) populat.......

Discussion

An optimized, validated FAPs isolation protocol for rat muscle is essential for researchers who wish to study injury models that are not feasible in the mouse for biologic or technical reasons. For example, mice are not an optimal animal model in which to study chronic local, or neurodegenerative injuries such as long-term denervation. Biologically, the short lifespan and rapid aging of mice make it difficult to accurately delineate the muscle sequalae due to denervation from the confounding factor of aging. From a techn.......

Acknowledgements

We would like to thank the Flow cytometry Core Facilities at the University of Ottawa and the Keenan Research Centre for Biomedical Sciences (KRC), St Michaels Hospital Unity Health Toronto for their expertise and guidance in optimization of the flow cytometry/FACS protocol presented in this manuscript. This work was funded by Medicine by Design New Ideas 2018 Fund (MbDNI-2018-01) to JB.

....

Materials

NameCompanyCatalog NumberComments
5 mL Polypropylene Round-Bottom TubeFalcon352063
5 mL Polystyrene Round-Bottom Tube with Cell-Strainer CapFalcon352235
10 cm cell culture dishesSarstedt83.3902
12-well cell culture plateThermoFisher130185
12 mm glass coverslips, No.2VWR89015-724
10 mL SyringeBeckton Dickenson302995
15 mL centrifuge tubesFroggaBio91014
20 gauge needleBeckton Dickenson305176
25mL Serological pipetteSarstedt86.1685.001
40µm cell strainerFisher Scientific22363547
50mL centrifuge tubesFroggaBioTB50
AbC Total Antibody Compensation Beads ThermoFisherA10497
Ammonium Chloride, Reagent GradeBioshopAMC303.500
APC Conjugation Kit, 50-100µgBiotium92307
Aquatex Aqueous Mounting MediumMerck108562
Biolaminin 411 LNBiolaminaLN411
Bovine Serum Albumin (BSA)BioshopALB001
Calcium ChlorideBioshopCCL444.500
Collagenase Type IIGibco17101015
CountBright Plus Absolute Counting BeadsThermoFisherC36995
DexamethasoneMillipore SigmaD4902
DispaseGibco17105041
Dulbecco’s Modified Eagle Medium (DMEM) (1X)Gibco11995-065(+)4.5 g/L D-Glucose
(+)L-Glutamine
(+)110 mg/L Sodium Pyruvate
EDTAFisherScientificS311
FACSClean SolutionBeckton Dickenson340345
FACSDiva SoftwareBeckton Dickenson--
FACSRinse SolutionBeckton Dickenson340346
Fetal Bovine SerumSigmaF1051
Flow Cytometry Sheath FluidBeckton Dickenson342003
FlowJo SoftwareBeckton Dickenson--
Fluorescent Mounting MediumDakoS302380-2
Goat anti-mouse Alexa Fluor 555 secondary antibodyInvitrogenA21424
Goat anti-rabbit Alexa Fluor 488 secondary antibodyInvitrogenA11008
Goat anti-rabbit Alexa Fluor 555 secondary antibodyInvitrogenA21429
Goat SerumGibco16210-064
Ham's F10 MediaThermoFisher 11550043(+) Phenol Red
(+) L-Glutamine
(-) HEPES
Hank’s Balanced Salt Solution (HBSS) (1X)Multicell311-513-CL
Heat Inactivated Horse SerumGibco26050-088
HemocytometerReichertN/A
HEPES, minimum 99.5% titrationSigmaH3375
Horse SerumThermoFisher16050130
Human Transforming Growth Factor β1 (hTGF-β1)Cell Signaling8915LF
Humulin RLillyHI0210
IBMXMillipore SigmaI5879Also known as 3-Isobutyl-1-methylxanthine
IsopropanolSigmaI9516Also known as 2-propanol
Lewis Rat, FemaleCharles River Kingston004 (Strain Code)200-250 grams used
LSRFortessa X-20 Benchtop CytometerBeckton Dickenson--
MicrocentrifugeEppendorfEP-5417R
MoFlo XDP Cell SorterBeckman Coulter--
Mouse Anti-CD31::FITC AntibodyAbcamab33858Clone TLD-3A12
Mouse Anti-CD45::FITC AntibodyBiolegend202205Clone OX-1
Mouse Anti-CD106::PE AntibodyBiolegend200403Also known as VCAM-1
Mouse Anti-MHC AntibodyDevelopmental Studies Hybridoma Bank (DSHB)N/AAlso known as MF20
Mouse Anti-Pax7 AntibodyDevelopmental Studies Hybridoma Bank (DSHB)N/A
Neutral Buffered Formalin, 10 %SigmaHT501128
Oil Red OMillipore SigmaO0625
PE-Cy7 Conjugation KitAbcamab102903
Penicillin-StreptomycinSigma P4333
Phosphate Buffered Saline, pH 7.4 (1X)Gibco10010-023(-)Calcium Chloride
(-)Magnesium Chloride
Potassium Bicarbonate, Reagent GradeBioshopPBC401.250
Rabbit Anti-Fibroblast Specific Protein 1 (FSP-1) AntibodyInvitrogenMA5-32347FSP-1 also known as S100A4
Rabbit Anti-Integrin-a7 AntibodyAbcamab203254
Rabbit Anti-Laminin AntibodySigmaL9393
Rabbit Anti-Perilipin-1 AntibodyAbcamab3526
Rabbit Anti-Sca-1 AntibodyMillipore SigmaAB4336
Rabbit Recombinant Anti-Collagen Type I AntibodyAbcamab260043Also known as Col1a1
Rabbit Recombinant Anti-PDGFR Alpha AntibodyAbcamab203491
Recombinant Human FGF-basicGibcoPHG0266
Sodium AzideSigmaS2002
Triton-X-100Fisher ScientificBP151
TroglitazoneMillipore SigmaT2573
Tween-20BioshopTWN510

References

  1. Joe, A. W. B., et al. Muscle injury activates resident fibro/adipogenic progenitors that facilitate myogenesis. Nature Cell Biology. 12, 153-163 (2010).
  2. Wosczyna, M. N., Biswas, A. A., Cogswell, C. A., Goldhamer, D. J.

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