Method Article

Isolation and Immortalization of Patient-derived Cell Lines from Muscle Biopsy for Disease Modeling

DOI:

10.3791/52307

January 18th, 2015

In This Article

Erratum Notice

Important: There has been an erratum issued for this article. View Erratum Notice

Summary

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This protocol describes techniques for live cell isolation and primary culture of myogenic and fibroblast cell lines from muscle or skin tissue. A technique for the immortalization of these cell lines is also described. Altogether, these protocols provide a reliable tool to generate and preserve patient-derived cells for downstream applications.

Abstract

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The generation of patient-specific cell lines represents an invaluable tool for diagnostic or translational research, and these cells can be collected from skin or muscle biopsy tissue available during the patient’s diagnostic workup. In this protocol, we describe a technique for live cell isolation from small amounts of muscle or skin tissue for primary cell culture. Additionally, we provide a technique for the immortalization of myogenic cell lines and fibroblast cell lines from primary cells. Once cell lines are immortalized, substantial expansion of patient-derived cells can be achieved. Immortalized cells are amenable to many downstream applications, including drug screening and in vitro correction of the genetic mutation. Altogether, these protocols provide a reliable tool to generate and preserve patient-derived cells for downstream applications.

Introduction

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Molecular diagnostics has dramatically evolved in the past 20 years. Genomic DNA is now routinely isolated from sputum or cheek swab, while in the past it required a blood draw. With the current fast turnaround time and ease of gene sequencing, many disease mutations are routinely identified with no need of additional testing. In the case of muscle disease diagnostics, identification of dozens of new genes in the past decade responsible for either muscular dystrophy or myopathy have dramatically changed the ways these diseases are diagnosed 1,2. Currently, there are dozens of genes that have been identified as causes of muscular dystrophy and congenital....

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Protocol

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NOTE: Protocols for collection of human tissue must be reviewed and approved by the Institutional IRB committee. Collection of discarded, de-identified human tissue has been approved by the Boston Children’s Hospital and Brigham and Women’s Hospital IRB Committees. The methods described below have been applied for the isolation of myogenic cells from de-identified, discarded tissue. The described methods are applicable to tissue collected from consented patient material.

1. Cell Isolation

  1. Dissociation of muscle biopsy and purification of myogenic cells
    1. Pre-weigh a 10 cm tissue culture plate in a tissue cu....

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Results

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Figure 1 illustrates some of the key steps involved in the primary tissue dissociation: the exact amount of tissue is weighed in a sterile tissue culture petri dish (Figure 1A, B). The tissue is then finely minced using sterile scalpels, until a tissue slurry is obtained (Figure 1C, D). Following addition of the digestion enzymes, primary muscle tissue dissociation is usually achieved by enzymatic digestion within 45-90 min. The progression of tissue digestion is typical.......

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Discussion

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Cells as a Useful Resource

The isolation and culture of myogenic cell populations is extremely useful when establishing disease phenotypes or in vitro models of disease. The myogenic cell isolation procedure described here allows the isolation of myoblasts and fibroblasts from skeletal muscle specimens, which can then be propagated, differentiated, or immediately analyzed. Myoblast structure and function can be assessed through microscopic examination, evaluation of cell survival, eva.......

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Disclosures

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The authors have nothing to disclose.

Acknowledgements

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This publication is funded through Cure CMD, an Association Contre Les Myopathies (AFM) grant (project 16297), and by the National Institutes of Health (grant numbers K08 AR059750, L40 AR057721 and 2R01NS047727).

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Equipment
Tissue culture biosafety hoodBaker Company, Inc.Model SterilGuard Hood
Benchtop centrifuge, such as Beckman Model Beckman CoulterModel Allegra 6RIf cell sorting is performed, a centrifuge with refrigeration is preferred
MicroscopeNikonModel Eclipse TS100
Tissue culture incubator, connected to a CO2 sourceForma Scientific Series II
Fluorescence-activated cell sorter (FACS)Becton DickinsonModel Aria
Reagents for isolation of primary myoblasts from tissue
Dispase IIRoche Applied Science#04942078001Prepare a sock solution of 2.4U/ml in DMEM
Collagenase D Roche Applied Science#088882001Prepare a stock solution of 10 mg/ml
1x Sterile Hank’s Balanced Saline Solution (HBSS), calcium and magnesium freeGIBCO Life Technologies#14185-052
Bovine serum albumin, fraction VSigma#05470Prepare a sterile  solution of 1X HBSS 0.5% BSA for FACS sorting
Sterile growth medium for myoblasts: Dulbecco’s Modified Eagle’s Medium (DMEM) with high glucose (4.5 g) supplemented with 30% fetal bovine serumGIBCO Life Technologies11965-092Contains L- glutamine
RBC lysis solutionQiagen158904
Propidium Iodide stock 10mg/mlSigmaP4170Prepare the stock solution by diluting the powder in sterile distilled water
Anti-human CD56 antibody for flow cytometryBiolegend318310APC-conjugated antibody, other labels are avaialable
Reagents for immortalization of primary myoblasts
Ecotropic packaging cell line PECell BiolabsRV-101
Amphotropic packaging cell line PA3174Cell BiolabsRV-102
Pig skin gelatinSigmaG1890-500gPrepare a stock solution of 0.1% gelatin in water. Coat the dish with the solution at 37°C for one hour. Remove the solution and add medium.
PolyJet SignagenSL100688
G418Fisher345812
HygromycinEMD Biosciences400051
pBabe plasmids containing mCDK4 and hTERTnot commercially availableStadler et al, 2013
Qiagen plasmid midiprep kitQiagen12143
Medium 199Life Technologies Medium 199 (31150022)
Dulbecco’s modified Eagle medium (DMEM)Life Technologies DMEM (11965-092)Mix 4:1 DMEM:199
Myoblast growth medium: 4:1 Dulbecco’s modified Eagle medium (DMEM) and Medium 199 supplemented with 15% fetal bovine serum; 0.02 M HEPES buffer; 1.4 mg/L vitamin B12; 0.03 mg/L ZnSO4, 0.055 mg/L dexamethasone, 2.5 μg/L hepatocyte growth factor and 10 μg/L beta fibroblast growth factor.Life technologie (DMEM, F199); Atlanta Biological (FBS); Invitrogen (Hepes); Fisher (ZincSulfate); Sigma (Vit.B12, Dexamethasone); Chemicon international (HGF); Biopioneer (betaFGF) #15630-080 (Hepes); #Z68-500 (ZnSO); #V2876.#D4902 (Vit.B12, Dex); GF116 (HGF); HRP-0011 (bFGF). Prepare media and stock solution Vit. B12 (20mg/ml); ZincSulfate (60µg/ml); Dex (55µg/µl) separately for easier use. HGF stock solution (5µg/ml) and FGF (20µg/ml) should be added freshly every week at the final working concentration.
TrypLE expressGIBCO Life Technologies12605-010
Myosin heavy chain antibody for immunostainingDevelopmental Hybridoma BankMF20Clone MF20
Desmin Antibody for immunostainingThermo ScientificMS-376-S0Clone D33
Horse serumInvitrogen26050-088
Reagents for primary skin fibroblast isolation
Transport medium: RPMI 1640 supplemented with 10% fetal bovine serum and 0.2% penicillin/streptomycinRPMI medium 1640: GIBCO Life Technologies11875-093
Human primary fibroblast culture medium: RPMI 1640 supplemented with 10% fetal bovine serum and 1% penicillin/streptomycinFetal bovine serum: Thermo ScientificSH30071.03
Collagenase solution: Collagenase type 2 (100 mg) resuspended in 12.5 ml of fibroblast culture medium and filter-sterilizedWorthington4176
Sterile 1X Phosphate Buffer Saline (PBS) calcium and magnesium freeLonza17-516F
Materials for isolation of primary myoblasts
50 ml and 15 ml sterile conical tubesGeneMate/BioexpressC-3394-4 (50 ml) ; C3394-1 (15 ml))
Sterile scalpelsAspen Surgical372610
HemocytometerHausser Scientific1492
Sterile 5, 10, and 25 ml pipettesBellco glass1226-05010 (5 ml); 1200-10010 (10 ml) ;1228-25050 (25 ml)Reusable pipettes are washed, cotton plugged and autoclaved before use
Sterile tissue culture-treated plastic dishes (10 cm)BD Falcon353003
Sterile nylon cell strainers (100 µm and 40 µm size)BD Falcon352340 (40µm); 352360 (100µm)
 Materials for myoblast immortalization
Sterile 0.45 µm filtersMilliporeSLHV013SL
Cloning ringsCorning#3166-8To be cleaned and autoclaved before and after use
Materials for fibroblast cell lines 
Sterile 35 mm tissue culture-treated plastic dishesGreiner bio-one628160
Sterile scalpelsDeRoyalD4510A
Sterile T25 tissue culture flasksTechno Plastic Product, TPP90026sold in the USA by MIDSCI
TrypLE expressGIBCO Life Technologies12605-010

References

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  1. Flanigan, K. M. The muscular dystrophies. Semin Neurol. 32, 255-263 (2012).
  2. Mercuri, E., Muntoni, F. Muscular dystrophies. Lancet. 381, 845-860 (2013).
  3. Sharples, A. P., Stewart, C. E.

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Erratum

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Formal Correction: Erratum: Isolation and Immortalization of Patient-derived Cell Lines from Muscle Biopsy for Disease Modeling
Posted by JoVE Editors on 11/12/2016. Citeable Link.

A correction was made to the authors section in: Isolation and Immortalization of Patient-derived Cell Lines from Muscle Biopsy for Disease Modeling

One of the authors names was corrected from:

Stacy C. Cossette

to:

Stacy A. Cossette

Tags

Muscle Biopsy IsolationCell Line ImmortalizationPrimary Cell CultureFACS PurificationMyogenic Cell DifferentiationCDK4 OverexpressionhTERT ExpressionViral Supernatant ProductionAntibiotic SelectionCloning Ring Technique

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