Method Article

Isolation and Characterization of Exosomes from Skeletal Muscle Fibroblasts

DOI:

10.3791/61127

⸱

May 16th, 2020

In This Article

Summary

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This protocol illustrates the 1) the isolation and culture of primary fibroblasts from the adult mouse gastrocnemius muscle as well as 2) purification and characterization of exosomes using a differential ultracentrifugation method combined with sucrose density gradients followed by western blot analyses.

Abstract

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Exosomes are small extracellular vesicles released by virtually all cells and secreted in all biological fluids. Many methods have been developed for the isolation of these vesicles, including ultracentrifugation, ultrafiltration, and size exclusion chromatography. However, not all are suitable for large scale exosome purification and characterization. Outlined here is a protocol for establishing cultures of primary fibroblasts isolated from adult mouse skeletal muscles, followed by purification and characterization of exosomes from the culture media of these cells. The method is based on the use of sequential centrifugation steps followed by sucrose density gradients. Purity of the exosomal preparations is then validated by western blot analyses using a battery of canonical markers (i.e., Alix, CD9, and CD81). The protocol describes how to isolate and concentrate bioactive exosomes for electron microscopy, mass spectrometry, and uptake experiments for functional studies. It can easily be scaled up or down and adapted for exosome isolation from different cell types, tissues, and biological fluids.

Introduction

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Exosomes are heterogeneous extracellular vesicles ranging in size from 30–150 nm. They are established key players in physiological and pathological processes, given their ubiquitous distribution in tissues and organs1,2. Exosomes carry a complex cargo of proteins, lipids, DNA types, and RNA types, which vary according to the type of cells from which they are derived1,2,3. Exosomes are enriched in proteins that have different functions (i.e., tetraspanins, including CD9 and CD63) are responsible for fusion event....

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Protocol

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All procedures in mice were performed according to animal protocols approved by the St. Jude Children’s Research Hospital Institutional Animal Care and Use Committee and National Institutes of Health guidelines.

1. Preparation of solutions and media

  1. Prepare digestion solution by mixing 15.4 mL of PBS with 2.5 mL of 20 mg/mL collagenase P (5 mg/mL final concentration), 2 mL of 11 U/mL dispase II (1.2 U/mL final concentration), and 100 µL of 1.0 M CaCl2 (5 mM final concentration).
  2. Prepare 500 mL of primary fibroblasts medium (DMEM complete) by mixing 440 mL of DMEM with 50 mL of FBS (10%), 5.0 mL of....

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Results

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This protocol is suitable for the purification of exosomes from large volumes of conditioned medium in a cost-effective manner. The procedure is highly reproducible and consistent. Figure 1 shows transmission electron microscopy (TEM) image of exosomes purified from the culture medium of mouse primary fibroblasts. Figure 2 shows the protein expression pattern of canonical exosomal markers, and the absence of cytosolic (LDH) and ER (calnexin) protein contaminants.......

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Discussion

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A critical step for the successful isolation of exosomes from the culture media, as outlined in this protocol, is the proper establishment and maintenance of primary mouse fibroblast cultures from adult skeletal muscle. These cultures need to be maintained at a low oxygen level to ensure physiological-like conditions (O2 level in skeletal muscle is ~2.5%)15. Primary fibroblasts will change characteristics when passed in culture too many times. Hence, a low passage number is imperative f.......

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Disclosures

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None of the authors have any conflicts of interest to declare.

Acknowledgements

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Alessandra d’Azzo holds the Jewelers for Children (JFC) Endowed Chair in Genetics and Gene Therapy. This work was supported in part by NIH grants R01GM104981, RO1DK095169, and CA021764, the Assisi Foundation of Memphis, and the American Lebanese Syrian Associated Charities.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
10 cm dishesMidwest Scientific, TPPTP93100
15 cm dishesMidwest ScientificTP93150
BCA protein assay kitThermo Fisher Scientific, Pierce23225
Bovine serum albumin Fraction VRoche10735094001
CaCl2SigmaC1016-100G
Centrifuge 5430R with rotors FA-35-6-30/ FA-45-48-11Eppendorf022620659/5427754008
Chemidoc MP imaging systemBioRad12003154
Collagenase PSigma, Roche11 213 857 001100 mg
cOmplete protease inhibitor cocktailMillipore/Sigma, Roche11697498001
Criterion Blotter with plate electrodesBioRad1704070
Criterion TGX stain-free protein gelBioRad567803410% 18-well, midi-gel
Criterion vertical electrophoresis cell (midi)BioRadNC0165100
Dispase IISigma, Roche04 942 078 001neutral protease, grade II
DithiothreitolSigma/Millipore, Roche10708984001
Dulbecco’s Modification Eagles MediumCorning15-013-CV
Dulbecco’s Phosphate Buffered SalineCorning21-031-CV
Ethanol 200 proofPharmco by Greenfield Global111000200
Falcon 50 mL conical centrifuge tubesCorning352070
Fetal Bovine SerumGibco10437-028
Fluostar Omega multi-mode microplate readerBMG Labtech
GlutaMAX supplementThermo Fisher Scientific, Gibco35050-061
Hydrochloric acidFisher ScientificA144S-500
Immobilon-P Transfer membranesMilliporeIPVH00010
Laemmli sample buffer (4x)BioRad1610747
Magnesium acetate solutionSigma63052-100ml
Non-fat dry milkLabScientificM-0842
O2/CO2 incubatorSanyoMC0-18M
Penicillin-StreptomycinThermo Fisher Scientific, Gibco15140-12210,000 U/ml
Premium microcentrifuge tubesFisher Scientific, Midwest ScientificAVSC15101.7 mL
Protected disposable scalpelsFisher Scientific, Aspen Surgical Bard-Parker372610
Running bufferBioRad1610732
Sodium ChlorideFisher Scientific, Fisher ChemicalS271-3
Stericup Quick release-GP sterile vacuum filtration systemMilliporeS2GPU05RE500 mL
Sterile cell strainer (70 mm)Fisher Scientific, Fisher brand22-363-548
SucroseFisher Scientific, Fisher ChemicalS5-500
SuperSignal west FemtoThermo Fisher Scientific34096
Thin wall Polypropylene tubesBeckman Coulter326823
Transfer bufferBioRad16110734
Trichloroacetic AcidSigma91228-100G
Tris baseBioRad1610719
Triton-X100 solutionSigma93443-100mL
TrypLE Express EnzymeThermo Fisher Scientific, Gibco12604-013No phenol red
Tween-20BioRad#1610781
Ultra-centrifuge Optima XPMBeckman CoulterA99842
Ultra-clear tube (14x89 mm)Beckman Coulter344059
Ultra-clear tubes (25x89 mm)Beckman Coulter344058
Water bath Isotemp 220Fisher ScientificFS220

References

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  1. Doyle, L. M., Wang, M. Z. Overview of Extracellular Vesicles, Their Origin, Composition, Purpose, and Methods for Exosome Isolation and Analysis. Cells. 8 (7), 727(2019).
  2. Gurunanthan, S., Kang, M. H., Jeyaraj, M., Qasim, M., Kim, J. H.

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Tags

Exosome IsolationSkeletal Muscle FibroblastsDifferential CentrifugationSucrose Density GradientWestern Blot AnalysisExosome CharacterizationPrimary Cell CultureConditioned MediumElectron MicroscopyMass Spectrometry

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