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

Podsumowanie

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.

Streszczenie

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.

Wprowadzenie

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 myopathy, although the mechanisms by which many of these genes produce disease remain unclear. In particular, rare diseases constitute a challenge due to the small size of the patient populations. For these cases, as well as for more common diseases, the generation of stable tools that facilitate studies on the mechanism of pathogenesis and screening of therapeutic drugs is highly desirable.

Despite dramatic progress in DNA diagnostics, muscle biopsies are still performed to establish the primary diagnosis in many patients in whom primary metabolic or muscle disease is suspected. When a muscle biopsy is necessary, it offers the opportunity for additional diagnostic and research tissue collection with minimal additional morbidity risk for the patient. As there are a number of uses for each tissue specimen, it is highly desirable to establish techniques for primary cell culture using surgical tissue that are straightforward, efficient, and require minimal amounts of tissue. Proper triage of muscle or skin biopsies is required to maximize isolation of primary cells from tissue and long-term storage of live material. Additionally, stem cell research and drug screening holds great promise for developing therapies for many diseases using cell-based assays ^3,4.

We herein describe methods for primary cell isolation from human muscle or skin biopsies. Additionally, we include a protocol for immortalization of myogenic cells, which is useful for generating large numbers of cells from an individual. These cells can be used for downstream applications, such as custom drug-screenings, which are otherwise unachievable with the overall low number of cells obtained from primary tissue.

Protokół

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 culture biosafety hood, and then re-weigh the plate containing the muscle biopsy to calculate the amount of tissue to be dissociated.
   2. Using sterile scalpels, mince muscle tissue finely and add a few drops of sterile 1x HBSS to prevent tissue from drying out.
   3. Add 3.5 ml each of dispase II and collagenase D per gram of muscle tissue to be digested. Pipette the minced tissue and enzyme solution through a sterile 25 ml pipette a few times. Incubate the plate in a tissue culture incubator at 37 °C with 5% CO₂ for 15 min and digest tissue until the slurry easily passes though a sterile 5 ml pipette.
      NOTE: Tissue dissociation is usually achieved by enzymatic digestion within 45-90 min. Please refer to the ‘Representative Results’ section for additional details.
   4. Add 2 volumes of sterile growth medium to dissociated tissue, filter through a 100 µm cell strainer over a 50 ml conical tube and pellet cells for 10 min at 329 x g (~1,100 rpm), room temperature. Please refer to the Materials Table for media composition.
   5. Resuspend the pellet in 1 volume of sterile growth medium and add 7 volumes red blood cell lysis solution. Filter the solution through a 40 µm cell strainer, then pellet the cells for 10 min at 329 x g, room temperature.
   6. Count the cells in a hemocytometer and resuspend the cells in 1x HBSS 0.5% BSA at a concentration of 1 x 10⁶ cells/100 µl. Set aside ~250,000 cells in a single tube that will be used as a negative (unstained) control. Set aside additional single-color stained control tubes for propidium iodide and for CD56, which are required for proper gating of CD56 positive cells by FACS sorting. Please refer to cell sorting manuals or consult with FACS sorting core facility experts to ensure appropriate controls are included.
   7. Stain the cells to be sorted with 5µl/10⁶ cells of anti CD56 antibody. Incubate all samples (including controls) on ice for 30 min.
   8. Wash samples in 10 ml 1x HBSS and pellet cells for 10 min at 329 x g (~1,100 rpm) in a refrigerated centrifuge, 4°C temperature.
   9. Add propidium iodide at a final concentration of 1µg/ml to the sample to be sorted for exclusion of dead cells. Purify myogenic CD56 positive cells from non-myogenic cells using the fluorescence activated cell sorter.
2. Dissociation of skin biopsy
   NOTE: Dermal fibroblasts can be isolated from a skin punch from patients when muscle biopsies are not available. Dermal fibroblasts can be used as biomaterial for many studies, including transduction with MyoD to generate myogenic cells. Additionally, dermal fibroblasts can be used to generate iPS cells, which can be differentiated into various cell types for further study.
   1. Transport the skin biopsy to the laboratory in transportation medium. Once the sample is received, perform the primary culture as soon as possible. If the primary culture cannot be established on the same day, store the sample at room temperature overnight.
   2. Transfer the skin biopsy to a sterile 35 mm petri dish in the laminar flow hood.
   3. Rinse the skin biopsy in a petri dish with sterile 1x PBS to remove blood and debris. Remove the adipose tissue with a sterile scalpel.
   4. Add 2 ml collagenase solution and mince the tissue with scalpel, incubate at 37 °C for 45 min to 1 hr, depending on the size of the tissue.
   5. Transfer the digested tissue to a 15 ml conical tube, rinse the petri dish with 2 ml of fibroblast culture medium twice, and collect the medium in the same tube.
   6. Pellet cells at 200 x g for 5 min at room temperature.
   7. Discard the supernatant and wash the pellet with 3 ml of fibroblast medium to remove the collagenase, then pellet cells again. Please refer to the Materials Table for media composition.
   8. Repeat the step 1.2.7 one more time.
   9. Re-suspend the pellet in 5 ml fibroblast medium and plate cells onto a T25 sterile tissue culture flask. Incubate the flask at 37 °C with 5% CO₂.
   10. Evaluate the culture for fibroblast attachment and growth over the next 1-3 days.
       NOTE: Some small tissue pieces may also attach to the plate and fibroblasts migrate out of these tissue pieces.
   11. Maintain the culture under the same conditions until fibroblasts are grown to approximately 80% confluence.
   12. Collect fibroblasts by trypsinization and transfer onto fresh culture flasks for additional expansion. Perform trypsinization by washing the cultures 3 times in 1x PBS free of Ca⁺⁺ and Mg⁺⁺. Add Trypsin-EDTA (see Materials Table) to the cells (2ml/ T25 flask) for 2 min at 37 °C.
   13. Split detached cells into additional flasks. If some tissue pieces remain attached to the original T25 flasks, add 5 ml fresh culture medium to this flask and more fibroblasts will migrate out continually.
       NOTE: The expanded fibroblast culture can be frozen down as P1 and stored in liquid nitrogen for future experiments.

2. Immortalization of Myogenic Cells

1. Plate 5 million Phoenix Ecotropic packaging cells (PE) overnight in a 10 cm sterile tissue culture plate in DMEM and Medium 199 in a ratio of 4:1, supplemented with 10% calf serum.
2. Feed cells 30 min prior to transfection with 5 ml of fresh media supplemented with 10 mM caffeine.
3. Homogenize a mixture of 2 μg of plasmid DNA from a midi prep (CDK4 or hTERT plasmid) and polyjet and incubate at room temperature for 15 min, as recommended by the manufacturer.
4. Add the plasmid/polyjet mixture to the PE cells overnight.
5. Feed cells with fresh medium (DMEM and Medium 199 in a ratio of 4:1, supplemented with 10% calf serum). Twelve hours later, collect the virus-containing supernatant and filter it through a 0.45 μm pore size filter.
6. Use 1 ml of collected supernatant to infect overnight the amphotropic packaging cell line PA317 ⁵ and obtain a stable virus-producing cell line after selection with either 0.5 mg/ml neomycin (G418) for CDK4 or 0.5 mg/ml hygromycin for hTERT.
7. Prepare working viral supernatants by growing the stable packaging cells to near confluency, then harvesting the supernatant each morning, evening and morning for three harvests.
8. Filter the viral supernatants and either directly use or divide them into 1 ml aliquots and store at -80 °C for later use. Note that viral supernatant loses 50% infection efficiency with each freeze-thaw. Remember to bleach-wash before discarding everything that has touched the viral particles.
   NOTE: The stable PA317 virus-producing cell line can be frozen and maintained at -150 °C for permanent storage (freezing medium is 10% DMSO; 90% Serum).
9. Plate FACS-purified myogenic cells (described in steps 1.1-1.9) at a density of 5 x 10⁴ cells/well in 6-well plates coated with 0.1% gelatin. Ensure that cells are attached to the plate before proceeding with the viral infection.
10. Add 400 μl filtered, freshly produced viral supernatant or frozen aliquots to each six-well plate overnight (keep 2 wells as controls).
11. Change medium by feeding cells with 2.5 ml/well of fresh muscle media (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 basic fibroblast growth factor). Discard the media and pipettes containing the viral particles in a bleach container. Leave cells in the same medium for 3 days to recover from infection, then treat for selection using either 400 μg/ml neomycin (CDK4 infection) or 300 μg/ml hygromycin (hTERT infection).
12. Maintain cells under drug selection until the cells in the control dish die (1-2 weeks).
13. Passage cells before they become confluent (60-80% confluency; using 0.05% trypsin EDTA), even during the selection period. Replate cells in multiple 10cm dishes with fresh myoblast medium (as described in 2.11) supplemented with the selection drug. Maintain immortalized selected cells as a heterogeneous population or clone to obtain a completely homogeneous genetic background (same insertion of the transgene in every cell).
14. Perform clonal selection using the following steps:
    1. Seed the cells at low density (e.g. 300 to 500 cells in 10 cm dishes) and maintain them for approximately two weeks, until small colonies are formed (10-20 cells).
    2. Remove most of the medium at this point, leaving only a thin film to prevent the cells from drying out.
    3. Place a cloning ring (with one end dipped in silicone vacuum grease) over each desired clone and add a few drops of trypsin/EDTA.
    4. Harvest cells once they become rounded by carefully aspirating the cells using a 1 ml tip or a Pasteur pipet and transferring them to the smallest available multiwell plate (96 or 48, 24 or 12 well plates).
    5. Expand clones as needed to prevent local confluency.

Wyniki

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...

Dyskusje

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...

Materiały

Name	Company	Catalog Number	Comments
Name of Material/ Equipment	Company	Catalog Number	Comments/Description
Equipment
Tissue culture biosafety hood	Baker Company, Inc.	Model SterilGuard Hood
Benchtop centrifuge, such as Beckman Model	Beckman Coulter	Model Allegra 6R	If cell sorting is performed, a centrifuge with refrigeration is preferred
Microscope	Nikon	Model Eclipse TS100
Tissue culture incubator, connected to a CO2 source	Forma Scientific	Series II
Fluorescence-activated cell sorter (FACS)	Becton Dickinson	Model Aria
Reagents for isolation of primary myoblasts from tissue
Dispase II	Roche Applied Science	#04942078001	Prepare a sock solution of 2.4U/ml in DMEM
Collagenase D	Roche Applied Science	#088882001	Prepare a stock solution of 10 mg/ml
1x Sterile Hank’s Balanced Saline Solution (HBSS), calcium and magnesium free	GIBCO Life Technologies	#14185-052
Bovine serum albumin, fraction V	Sigma	#05470	Prepare 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 (4.5g) supplemented with 30% fetal bovine serum	GIBCO Life Technologies	11965-092	Contains L- glutamine
RBC lysis solution	Qiagen	158904
Propidium Iodide stock 10mg/mL	Sigma	P4170	Prepare the stock solution by diluting the powder in sterile distilled water
Anti-human CD56 antibody for flow cytometry	Biolegend	318310	APC-conjugated antibody, other labels are avaialable
Reagents for immortalization of primary myoblasts
Ecotropic packaging cell line PE	Cell Biolabs	RV-101
Amphotropic packaging cell line PA3174	Cell Biolabs	RV-102
Pig skin gelatin	Sigma	G1890-500g	Prepare 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	Signagen	SL100688
G418	Fisher	345812
Hygromycin	EMD Biosciences	400051
pBabe plasmids containing mCDK4 and hTERT	not commercially available		Stadler et al, 2013
Qiagen plasmid midiprep kit	Qiagen	12143
Medium 199	Life 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 express	GIBCO Life Technologies	12605-010
Myosin heavy chain antibody for immunostaining	Developmental Hybridoma Bank	MF20	Clone MF20
Desmin Antibody for immunostaining	Thermo Scientific	MS-376-S0	Clone D33
Horse serum	Invitrogen	26050-088
Reagents for primary skin fibroblast isolation
Transport medium: RPMI 1640 supplemented with 10% fetal bovine serum and 0.2% penicillin/streptomycin	RPMI medium 1640: GIBCO Life Technologies	11875-093
Human primary fibroblast culture medium: RPMI 1640 supplemented with 10% fetal bovine serum and 1% penicillin/streptomycin	Fetal bovine serum: Thermo Scientific	SH30071.03
Collagenase solution: Collagenase type 2 (100mg) resuspended in 12.5 ml of fibroblast culture medium and filter-sterilized	Worthington	4176
Sterile 1X Phosphate Buffer Saline (PBS) calcium and magnesium free	Lonza	17-516F
Materials for isolation of primary myoblasts
50ml and 15ml sterile conical tubes	GeneMate/Bioexpress	C-3394-4 (50ml) ; C3394-1 (15ml))
Sterile scalpels	Aspen Surgical	372610
Hemocytometer	Hausser Scientific	1492
Sterile 5, 10 and 25 ml pipettes	Bellco glass	1226-05010 (5ml); 1200-10010 (10ml) ;1228-25050 (25ml)	Reusable pipettes are washed, cotton plugged and autoclaved before use
Sterile tissue culture-treated plastic dishes (10cm)	BD Falcon	353003
Sterile nylon cell strainers (100µm and 40µm size)	BD Falcon	352340 (40µm); 352360 (100µm)
Materials for myoblast immortalization
Sterile 0.45µm filters	Millipore	SLHV013SL
Cloning rings	Corning	#3166-8	To be cleaned and autoclaved before and after use
Materials for fibroblast cell lines
Sterile 35mm tissue culture-treated plastic dishes	Greiner bio-one	628160
Sterile scalpels	DeRoyal	D4510A
Sterile T25 tissue culture flasks	Techno Plastic Product, TPP	90026	sold in the USA by MIDSCI
TrypLE express	GIBCO Life Technologies	12605-010