Exon Skipping in Directly Reprogrammed Myotubes Obtained from Human Urine-Derived Cells

Summary

In this article, we describe a detailed protocol for efficient modelling of Duchenne muscular dystrophy muscle using MYOD1-converted urine-derived cells to evaluate the restoration of dystrophin mRNA and protein levels after exon skipping.

Abstract

Duchenne muscular dystrophy (DMD), a progressive and fatal muscle disease, is caused by mutations in the DMD gene that result in the absence of dystrophin protein. To date, we have completed an investigator-initiated first-in-human study at the National Center of Neurology and Psychiatry based on the systemic injection of the morpholino oligonucleotides which are prone to exon-53 skipping. For the effective treatment of DMD, in vitro testing with myoblasts derived from DMD patients to screen drugs and assess patient eligibility before undertaking clinical trials is thought to be essential. Very recently, we reported a new MYOD1-converted urine-derived cell (UDC) treated with the histone methyltransferase inhibitor (3-deazaneplanocin A hydrochloride), as a cellular model of DMD. The new autologous UDC might show phenocopy of the disease-specific phenotypes of DMD, leading to the application of precision medicine in a variety of muscle-related diseases. In this article, we describe a detailed protocol for efficient modelling of DMD muscle cells using MYOD1-converted UDCs along with reverse transcriptase polymerase chain reaction (RT-PCR), Western blotting, and immunocytochemistry to evaluate the restoration of dystrophin mRNA and protein levels after exon skipping.

Introduction

Duchenne muscular dystrophy (DMD), a progressive, fatal muscle disease, is caused by frame-shift mutations in the DMD gene that result in the absence of dystrophin protein¹. Antisense oligonucleotide-based exon skipping therapy is thought to be promising for DMD. This therapy is based on the conversion of the severer DMD phenotype to the milder Becker muscular dystrophy-like phenotype by altering pre-mRNA splicing to restore the DMD reading frame². We have recently completed a first-in-human study based on repeated intravenous administration of the phosphorodiamidate morpholino oligomer (PMO) viltolarsen, which can induce exon 53 skipping in DMD, and demonstrated an excellent safety profile, promising efficacy, and acceptable pharmacokinetic parameters (registered as UMIN: 000010964 and ClinicalTrials.gov: NCT02081625)³.

However, to develop cost-effective and efficient treatments for the disease, in vitro tests using primary muscle cells obtained from DMD patients are essential for drug screening and patient eligibility verification before undertaking clinical trials, as well as biomarkers that reflect the efficacy of exon skipping therapies during human trials⁴. Very recently, we reported a novel technology to develop patient-specific MYOD1-converted urine-derived cells (UDCs)^5,6 as a primary myoblast model of DMD⁷. Thus, to generate the myoblasts, only the collection of urine from patients is required and no invasive procedure is needed. In this article, we describe a detailed protocol for efficient modelling of DMD muscle using MYOD1-converted UDCs treated with 3-deazaneplanocin A hydrochloride to evaluate the restored dystrophin mRNA and protein after exon skipping.

Protocol

The Ethics Committee of the National Center of Neurology and Psychiatry approved this study (approval ID: A2017-018, A2018-029). All individuals gave informed consent before providing urine. All experiments were performed under the relevant guidelines and regulations.

1. Isolation and primary culture of UDCs

NOTE: UDCs were isolated according to a previously published protocol^8,9,10 with some modifications.

1. Collect urine samples during spontaneous micturition in sterilized plastic bottles.
   NOTE: Sterilization of the external urethral orifice is not needed. Midstream urine is desirable to reduce the risk of viral contamination. If the stock time before the next procedure is >1 h, urine samples should be transferred to 4 °C to preserve the cell viability. However, a temperature of <4 °C should be avoided because insoluble precipitates may appear.
2. Centrifuge the entire urine sample at 400 x g for 10 min at room temperature.
3. Aspirate the supernatant, leaving 1 mL in the tube.
4. Resuspend the pellets individually in the remaining 1 mL of urine and then collect those in a single 50 mL tube.
5. Add 10 mL of washing buffer consisting of 99 mL of PBS without calcium and magnesium, 1% penicillin/streptomycin (P/S), 0.5 µg/mL amphotericin B, and centrifuge the samples at 200 x g for 10 min at room temperature.
6. Aspirate the supernatant, leaving 0.2 mL in the tube.
7. Resuspend the cell pellets in 4.5 mL of primary medium composed of a 1:1 mixture of high glucose Dulbecco's modified Eagle medium (DMEM)without sodium pyruvate and Ham's F-12 nutrient mix supplemented with recombinant human epidermal growth factor (EGF), insulin, hydrocortisone, epinephrine, T3, transferrin, 10% tetracycline-free fetal bovine serum (FBS), 1% P/S, and 0.5 µg/mL amphotericin B.
8. Seed the cells in three wells of gelatine-coated six well plates (total volume of each well, 1.5 mL). Culture humidified at 37 °C and 5% CO₂ for 24 h.
9. Add 1.5 mL of the primary medium daily for the next 3 days.
10. On day 4, replace the medium with 1.5 mL of growth medium supplemented with recombinant human EGF, insulin, hydrocortisone, epinephrine, T3, transferrin, 15% tetracycline-free FBS, 0.5% L-alanine-L-glutamine, 0.5% nonessential amino acids, and 2.5 ng/mL fibroblast growth factor-basic (bFGF), recombinant human platelet-derived growth factor (PDGF), EGF, and 1% P/S.
11. Change the growth medium every other day.
    NOTE: UDC colonies appear within a week.
12. When the UDC culture becomes 80−90% confluent, remove the medium and wash cells with PBS, split all the cells using 0.25% trypsin-EDTA and seed at 3,000-5,000 cells/cm² onto a new gelatine-coated 60 mm dish (passage 1).
    NOTE: The UDCs can be stored in liquid nitrogen. UDCs are usually divided at 60−70% confluency in 60 mm culture dish into three stock tubes.

2. Retroviral construct

1. Amplify the coding region of MYOD1 (NM_002478.4) plasmid by polymerase chain reaction (PCR).
   NOTE: The mixture for MYOD1 amplification and conditions for the thermal cycler are shown in Table 1 and Table 2, respectively.
2. Detect a single band of about 1,000 bp size by 0.7% agarose gel electrophoresis using 1 µL of the amplified PCR product to confirm that the MYOD1 sequence is amplified successfully.
3. Clean the PCR product using the clean-up kit and determine its concentration with a spectrophotometer.
4. Incubate the mixture as shown in Table 3 at 37 °C overnight to digest retroviral vector with a Tet-on system and puromycin resistant gene at restriction enzyme-targeted regions in the multiple cloning site.
5. Detect a single band by 0.7% agarose gel electrophoresis using 1 µL of the digested product to confirm that the retroviral vector was digested successfully.
6. Clean the digested product using clean-up kit and determine its concentration by spectrophotometer.
7. To clone the amplified MYOD1 fragment (produced by steps 2.1−2.3) into the digested retroviral vector (produced by steps 2.4−2.6), perform an in-fusion cloning reaction. Set up the reaction as shown in Table 4, incubate the reaction for 15 min at 50 °C, and then place on ice.
8. Perform transformation using E. coli competent cells according to the manufacturer's instructions (Table of Materials).
9. Select the transformed competent cells by culturing on an LB culture plate consisting of 10 g/L bacto tryptone, 5 g/L bacto yeast extract, 5 g/L NaCl, 15 g/L bacto agar, and 50 mg/L ampicillin.
10. Pick up the selected colony and culture in LB culture medium without bacto agar at 200 rpm at 37 °C overnight.
11. Purify the MYOD1-inserted retroviral vectors using a plasmid purification kit (Table of Materials) and quantify using a spectrophotometer.
12. Confirm that MYOD1 is correctly inserted into the retroviral vector by direct sequencing of the PCR product amplified by the forward and reverse primers targeted respectively on both sides across the inserted MYOD1 sequence.
    NOTE: The MYOD1 sequence can be detected sandwiched between retroviral vector sequences when in-fusion cloning is successful.
13. For retroviral production, seed the packaging cells at 50,000 cells/cm² on 10 cm collagen-coated plates and culture in DMEM with 10% FBS humidified at 37 °C and 5% CO₂ for 24 h.
14. When the packaging cells proliferate to 80% confluency, mix 30 µg of MYOD1-inserted retroviral vectors, 30 µg of packaging vectors, and transfection reagent containing cell-penetrating peptide (Table of Materials) by vortexing, and incubate them for 10 min.
15. Add the incubated mixture to the medium of packaging cells and culture humidified at 37 °C and 5% CO₂.
    NOTE: Collagen coating is necessary. Transfection may be better at 24 h or more after seeding because packaging cells easily detach from the culture plate.
16. After 4 h or overnight, change the medium to fresh growth medium.
17. Collect the viral supernatant and replace with fresh medium at 24 and 48 h after cotransfection and combine the supernatant.
18. To concentrate the viral supernatant, mix it with the concentrator reagent and incubate at 37 °C overnight, then centrifuge at 1,500 x g for 45 min at 4 °C.
19. Filter the retrovirus supernatant through a PVDF filter with 0.45 µm pores.
20. Check the titer of the retroviral vector using a quantitative PCR kit and thermal cycler system according to the manufacturer's instructions.
21. Divide the viral supernatant into small aliquots and stock them at -80 °C.

3. Infection with MYOD1-retroviral vector in UDCs

1. Seed the UDCs at 3,000-5,000 cells/cm² on a gelatine-coated 60 mm dish.
2. After 24 h of seeding, infect the thawed retrovirus (step 2.21) at a multiplicity of infection of 200 by adding hexadimethrine bromide at a concentration of 8 µg/mL.
3. After a 24 h incubation humidified at 37 °C and 5% CO₂, replace the culture medium with fresh growth medium containing 1 µg/mL puromycin to select the MYOD1-transduced cells. Change the medium every other day.
   NOTE: When selecting for MYOD1-positive cells, 1 µg/mL puromycin is usually used for selection. The appropriate dose should be determined. Use a plate containing untransfected cells and choose the dose that kills all the cells in 3−5 days. MYOD1-positive cells should be selected within 7−10 days after adding puromycin. The MYOD1-transduced UDCs can be stored in liquid nitrogen.

4. Myogenic differentiation of MYOD1-transduced UDCs treated with 3-deazaneplanocin A hydrochloride (DZNep)

NOTE: Recently, it has been reported that DZNep, a histone methyltransferase inhibitor, could significantly promote the expression of MYOGENIN, one of the late muscle regulatory factors, and also lead to myotube differentiation⁷.

1. Plate MYOD1-transduced UDCs in the collagen-coated wells at a density of 3.5 x 10⁴ cells/cm². Culture humidified at 37 °C and 5% CO₂.
2. After 24 h, change the growth medium to differentiation medium composed of high glucose DMEM with L-alanine-L-glutamine, 5% horse serum, ITS supplement, 1 µg/mL doxycycline, and 5 µM DZNep.
   NOTE: The 10 mM DZNep solution can be stored at -80 °C for 3 months. Use a defrost freezer and avoid repeated freeze-thaw cycles. Both MYOD1 activated by doxycycline and DZNep suppress proliferation and promote the myogenic differentiation of UDCs. Therefore, it is recommended that doxycycline and DZNep are added after the induction of myogenic differentiation. DZNep promotes myogenic differentiation of the MYOD1-UDCs in a dose-dependent manner. On the other hand, it shows cytotoxicity at a high concentration. Therefore, determine the appropriate concentration of DZNep, ranging from 1−10 µM depending on its effects on myogenic differentiation and cellular bioavailability.
3. After 3 days, change the differentiation medium to fresh differentiation medium without DZNep. Then, change the medium every 3 days.
   NOTE: UDCs fuse to each other and form myotubes within 1−2 weeks after differentiation.

5. Exon skipping in MYOD1-converted UDCs

NOTE: Here, three protocols are described to evaluate exon skipping in patient-derived cells: 1) reverse transcriptase polymerase chain reaction (RT-PCR) of dystrophin mRNA; 2) semiquantification of restored dystrophin protein signal by Western blot; and 3) semiquantification of restored dystrophin fluorescence signal by immunocytochemistry. All the methods can detect exon skipping in a dose-dependent manner.

1. Evaluation of exon skipping efficiency by RT-PCR
   1. To transfect antisense oligonucleotide (ASO) into MYOD1-converted UDCs obtained from DMD patients on the day 7 after differentiation, mix ASO, transfection reagent (Table of Materials), and differentiation medium to a final concentration of 1−10 µM. Culture humidified at 37 °C and 5% CO₂.
   2. After 72 h of incubation with ASO, change the medium to fresh differentiation medium without ASO.
   3. From 3−7 days after ASO transfection, remove differentiation medium and wash 1x with PBS. Add cell lysis buffer, lyse the UDCs and harvest the total RNA using an RNA extraction kit.
   4. Measure the RNA concentration with a spectrophotometer.
   5. Combine the required reagents for one-step RT-PCR reaction in PCR tubes according to Table 5.
   6. Place the PCR tubes with the mixture in a thermocycler. Run the thermocycler, according to Table 6.
   7. Perform microchip electrophoresis and calculate the exon skipping efficiency using the molar concentration as below.
      Exon skipping efficiency (%) = skipped band / (skipped band + non-skipped band) x 100
      NOTE: Store the PCR product in a refrigerator at 4 °C for short-term storage or -20 °C for long-term storage.
2. Detection of dystrophin after exon skipping by Western blotting
   1. Transfect ASO and culture MYOD1-UDCs according to steps 5.1.1 and 5.1.2.
   2. Change the medium every 3 days.
   3. After 2 weeks of differentiation, extract the total protein from the cultured cells using radioimmunoprecipitation assay (RIPA) buffer containing protease inhibitors.
   4. Sonicate the lysates on ice and centrifuge at 14,000 x g for 15 min at 4 °C.
   5. Collect the supernatant and determine protein concentrations using a BCA protein assay kit.
   6. Add 15 µg of total protein in a 0.5 mL tube and dilute by adding the RIPA buffer containing protease inhibitors to a total volume of 10 µL. Run 15 µg of total protein per lane.
   7. Add sample buffer, reducing agent, and deionized water as shown in Table 7. Denature the cell lysates at 70 °C for 10 min.
   8. Prepare the tris-acetate running buffer containing 8.95 g/L tricine, 6.06 g/L tris base, 1.0 g/L sodium dodecyl sulfate (SDS).
   9. Load the sample (20 µL) onto tris-acetate 3−8% gel and perform electrophoresis at 150 V for 75 min.
   10. Prepare the blotting buffer without methanol.
   11. Soak the PVDF membrane for 20 s in methanol and then in the blotting buffer until use (at least 10 min). Cut the PVDF membrane to a size of 6 x 8 cm using mini gels and 8 x 12 cm using midi gels.
   12. Cut the blotting papers to the same size as that of the PVDF membrane and soak those in the blotting buffer until use.
   13. After electrophoresis, cut the gel to the same size as that of the PVDF membrane and soak the gel in distilled water.
   14. Place the blotting papers, PVDF membrane, and gel on the semidry transfer apparatus (Figure 1). Transfer at 4 mA/cm² for 30 min.
   15. Rinse the membrane 2x with distilled water.
   16. Prepare anti-dystrophin (1:500) and anti-α-tubulin (1:1,200) antibody as the primary antibodies.
   17. Prepare HRP-conjugated anti-mouse antibody (1:100) as a secondary antibody.
   18. Incubate the membranes with the primary antibodies, wash with wash buffer, then incubate with the secondary antibody using an automated Western-processing device (Table of Materials) at room temperature.
       NOTE: Anti-α-tubulin antibody is usually used as a loading control. The mixed primary antibody solutions, including 1:500 anti-dystrophin and 1:1,200 anti-α-tubulin antibodies work well when the antibody reaction is performed simultaneously.
   19. Rinse the membrane in distilled water.
   20. Detect the proteins using chemiluminescent detection reagent and a charge-coupled device (CCD) camera-based imager.
   21. Analyse the data using appropriate software.
3. Detection of dystrophin after exon skipping by immunocytochemistry
   1. Directly reprogram the UDCs into the myotubes in collagen-coated 96 well plate according to steps 4.1−4.3.
   2. Transfect the ASO and culture MYOD1-UDCs according to steps 5.1.2 and 5.1.3.
   3. After 2 weeks of differentiation, wash the cells with PBS and fix them in 4% paraformaldehyde for 10 min at 4 °C.
   4. Permeabilize MYOD1-UDCs in 0.1% nonionic detergent for 10 min at room temperature and block those with 10% goat serum for 15 min at 37 °C.
   5. Incubate the cells with a primary antibody overnight at 4 °C.
   6. Wash the cells with PBS and incubate those with the secondary antibody for 30 min at room temperature.
      NOTE: Here, mouse anti-dystrophin (1:30) is used as the primary antibody, anti-mouse IgG is used as the secondary antibody, and Hoechst (1:10,000) is used for nuclei staining.
   7. Image the plates using a fluorescent microscope and use an analyzer to semiquantify the fluorescence signal automatically in every well under the same condition.

Representative Results

We could collect the UDCs easily and non-invasively. UDCs formed colonies within a week after starting primary cell culture we observed a marked proliferative ability. The culture of UDCs was straightforward, and bacterial or fungal contamination was rare when the procedure was performed correctly.

Figure 2 shows representative phase-contrast images of the UDC colony a week after primary culture (Figure 2A) and MYOD1-UDCs a week after differentiation (Figure 2B). Figure 3 shows the successful detection of exon skipping in UDCs obtained from DMD patients by RT-PCR. Figure 3A shows RT-PCR analysis of dystrophin after antisense oligonucleotide treatment in DZNep-treated MYOD1-UDCs derived from a 6-year-old male with an exon 45-54 deletion in the DMD gene. The open reading frame was restored by exon 44 skipping. On day 14 following differentiation, we confirmed the induction of exon skipping in a dose-dependent manner (Figure 3B). The upper bands denote native products, and the lower bands denote exon 44-skipped products that restored the open reading frame.

Figure 4 shows the successful detection of dystrophin after exon skipping in the UDCs obtained from DMD patients by Western blotting in a dose-dependent manner. We also detected the restored dystrophin expression using immunocytochemistry (Figure 5). We measured the intensities of dystrophin with a fluorescent microscope 1 week after the antisense oligonucleotide (ASO) transfection on a 96 well plate (Figure 5A). Markedly higher fluorescent signals were observed in MYOD1-UDCs treated with ASO than in MYOD1-UDCs treated with control ASO (Figure 5B).

These results suggest that our new assay can evaluate exon skipping efficiently in MYOD1-UDCs obtained from DMD patients at the mRNA and protein level.

Figure 1: Schematic representation of the transfer stack for semidry Western blot. Two papers soaked in the blotting buffer were laid down at the negative terminal, and two papers soaked in the buffer were stacked on top of this. The gel, which has been soaked in the buffer, was laid gently over the PVDF membrane. Please click here to view a larger version of this figure.

Figure 2: Representative images of the UDCs. (A) Phase-contrast image of UDCs a week after primary culture. Scale bar = 200 µm. Inset: A magnified image of the area in the white rectangle. (B) Phase-contrast image of MYOD1-UDCs a week after differentiation. Scale bar = 50 µm. This figure has been modified from Takizawa et al.⁷. Please click here to view a larger version of this figure.

Figure 3: Successful evaluation of exon skipping in urine-derived cells (UDCs) obtained from DMD patients by RT-PCR. (A) RT-PCR analysis of dystrophin after antisense oligonucleotide treatment in 3-deazaneplanocin A hydrochloride (DZNep)-treated MYOD1-UDCs derived from Duchenne muscular dystrophy (DMD) patient with an exon 45-54 deletion. DZNep-treated MYOD1-UDCs were also treated with the control antisense at 1-10 µM concentration as controls. The upper bands were unskipped products (Ex 45-54 deletion) that remained out of the reading frame. The lower bands were the exon 44-skipped products (Ex 44-54 deletion and Ex 44 skipped) that restored the open reading frame. (B) Skipping efficiency was calculated as (exon 44-skipped transcript molarity)/(native + exon 44-skipped transcript molarity [marked with arrows]) x 100% using a microchip electrophoresis system. One-way ANOVA followed by Bonferroni's post hoc test was used to compare the skipping efficiencies (n = 3 for each group, ****P < 0.0001). The data are expressed as the mean ± SEM. This figure has been modified from Takizawa et al.⁷. Please click here to view a larger version of this figure.

Figure 4: Successful evaluation of exon skipping in urine-derived cells (UDCs) from DMD patients by Western blot. (A) Representative Western blot for dystrophin in DZNep-treated MYOD1-UDCs from DMD patient with an exon 45-54 deletion after exon 44 skipping. For dystrophin detection, anti-dystrophin (against C-terminal) was used. (B) The relative intensities of the bands normalized to α-tubulin expression were compared in patient-derived cells with and without antisense oligonucleotide treatment by performing one-way ANOVA followed by Bonferroni's post hoc test (n = 3 for each group, **P < 0.01, ***P < 0.001, HI = healthy individual). This figure has been modified from Takizawa et al.⁷. Please click here to view a larger version of this figure.

Figure 5: Heatmaps of immunocytochemistry for dystrophin after antisense oligonucleotide treatment in DZNep-treated MYOD1-UDCs obtained from DMD patient with exon 45-54 deletion. (A) Deletion of exon 45-54 restored the open reading frame based on the exon skipping of exon 44. (B) The signal intensity was quantified using a fluorescent microscope after 1 week of antisense oligonucleotide transfection on a 96 well plate. One-way ANOVA followed by Bonferroni's post hoc test was used for the comparison (n = 3-4 for each group, ****P < 0.0001). This figure has been modified from Takizawa et al.⁷. Please click here to view a larger version of this figure.

Reagent	Volume	Final concentration
2x PCR premix	12.5 μL	1x
Forward primer	5 pmol	0.2 μM
Reverse primer	5 pmol	0.2 μM
Template	80 ng
Sterilized distilled water	up to 25 μL
Total volume per reaction	25 μL

Table 1: Mixture for MYOD1 amplification by RT-PCR.

98 °C	10 s
55 °C	10 s	} 35 cycles
72 °C	10 s

Table 2: Conditions for the thermal cycler for MYOD1 amplification.

Reagent	Volume
10x K buffer	2 μL
Retroviral vector (500 ng/μL)	2 μL
Restriction enzyme 1 (2−15 U)	1 μL
Restriction enzyme 2 (2−15 U)	1 μL
Sterilized distilled water	14 μL
Total volume	20 μL

Table 3: Mixture for a tube to digest retroviral vector.

Reagent	Volume
Purified MYOD1 fragment	100 ng
Digested retroviral vector	100 ng
5x Enzyme premix	4 μL
Sterilized distilled water	up to 20 μL
Total volume	20 μL

Table 4: Mixture for the in-fusion cloning reaction.

Solution	Volume/Reaction (μL)	Final concentration
RNase-free water	Variable	-
One-step RT-PCR buffer	4	1x
dNTP mix (containing 10 mM of each dNTP)	0.8	400 mM of each dNTP
Forward primer (10 mM)	1.2	0.6 mM
Reverse primer (10 mM)	1.2	0.6 mM
One-step RT-PCR enzyme mix	0.8	-
RNase inhibitor (optional)	Variable	5−10 units/reaction
Template RNA	50−400 ng
Total volume	20

Table 5: Necessary compounds for one reaction of the one-step RT-PCR.

1 cycle	Reverse transcription	30 min	50 °C
1 cycle	Initial PCR activation step	15 min	95 °C
1 cycle	Denaturation	1 min	94 °C
	Annealing	1 min	60 °C
	Extension	1 min	72 °C
1 cycle	Final extension	7 min	72 °C
Hold		∞	4 °C

Table 6: Thermal cycler condition for one-step RT-PCR.

Reagent	Volume
Protein (15 μg)	10 μL
Sample buffer (4x)	5 μL
Reducing agent (10x)	2 μL
Deionized water	3 μL
Total volume	20 μL

Table 7: Preparation of samples for sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE).

Discussion

Here, we describe a detailed protocol of exon skipping in MYOD1-converted UDCs obtained from DMD patients. Using the assay system, we screened optimal antisense sequences efficiently. We assume that MYOD1-converted UDCs can be useful for the investigation of the pathophysiology of the disease.

Evaluation of exon skipping using patient-derived cells at the mRNA level is indispensable for screening new drugs and assessing patient eligibility before undertaking clinical trials. Calculation of exon skipping efficiency can be evaluated only at an mRNA level.

Evaluation of exon skipping at the protein level is also important because dystrophin restoration is important as a surrogate biomarker to predict the benefits of exon skipping. To date, screening of antisense oligonucleotide sequences is often performed using primary muscle cell lines or immortalized myoblast cell lines including human rhabdomyosarcoma (RD) cells, but we cannot measure the recovery of dystrophin levels using muscle cell lines or RD cell lines because they express this protein endogenously. We can clearly detect the restoration of dystrophin in DMD patient-derived MYOD1-UDCs in a dose-dependent manner. In our new assay, we consider that the evaluation of restored protein by Western blotting is superior in quantifiability. On the other hand, evaluation by immunocytochemistry using 96 well plates is ideal for screening many candidate compounds simultaneously.

In this article, we describe a detailed protocol for an efficient modelling DMD muscle using MYOD1-converted UDCs along with RT-PCR, Western blotting, and immunocytochemistry to evaluate the restored dystrophin at the mRNA and protein levels after exon skipping. UDCs can be collected noninvasively and easily. Therefore, we assume that the brand-new in vitro assay can be applied to a wide range of basic and translational studies regardless of the type of muscular disorders.

Materials

Name	Company	Catalog Number	Comments
1% P/S Solution Stabilized	Thermo Fisher	15070-063	Cell culture
Amphotericin B	Sigma Aldrich	A2942
Anti-dystrophin	Abcam	ab15277	Western blot (WB)
Anti-dystrophin	Leica	NCL-DYS1	Immunocytochemistry(ICC)
Anti-mouse IgG, Dylight 488	Vector Laboratories	DK-2488	ICC
Anti-α-tubulin	Sigma	T6199	Western bot and ICC
BZ-X800	KEYENCE	BZ-800	Fluorescent microscope
CELLBANKER	ZENOAQ	CB011	Cell stock in liquid nitrogen
ChemiDoc MP Imaging System	Bio-Rad	170-8280J1	WB
CloneAmp HiFi PCR premix	Clontech	639298	Retroviral production
cOmplete Protease Inhibitor Cocktail	Roche	4693116001	Protein extraction for WB
E.coli DH5 α Competent Cells	TAKARA	9057
ECL Prime Western Blotting Detection Reagent	GE healthcare	RPN2232	WB
EGF	Peprotech	AF-100-15	Cell culture
Endo-Porter	GeneTools	2922498000	ASO transfection
Extra Thick Blot Filter Paper	Bio-Rad	1703965	WB
EzFastBlot HMW	Atto	AE-1460	WB
fibroblast growth factor-basic	Sigma-Aldrich	F0291	Cell culture
Glutamax	Thermo Fisher Scientific	35050-061	Cell culture
GP2-293 packaging cells	Clontech	631458	Retroviral production
Ham's F-12 Nutrient Mix	Thermo Fisher Scientific	11765-054	Cell culture
High glucose DMEM with GlutaMAX-I	Thermo Fisher Scientific	10569-010	Cell culture
High glucose DMEM without sodium pyruvate	GE Healthcare	SH30022.01	Cell culture
HiSpeed Plasmid Purification Kit	QIAGEN	12643	Retroviral production
Histofine Simple Stain MAX PO	NICHIREI BIOSCIENCE INC.	424151	WB
Hoechst 33342	Thermo Fisher Scientific	H3570	ICC
Human PDGF-AB	Peprotech	100-00AB-10UG	Cell culture
iBind Flex Solution	Thermo Fisher Scientific	SLF2020	WB
iBind Flex Western Device	Thermo Fisher Scientific	SLF2000	WB (Automated mestern-processing device)
Immobilon-P Transfer Membrane (PVDF)	MERCK	IPVH304F0	WB
In-Fusion HD cloning Kit	Clontech	639648	Retroviral production
ITS Liquid Media Supplement	Sigma-Aldrich	I3146	Cell culture
MILTEX HV 0.45 μm filter	MERCK	SLHV033RS	Retroviral production
MultiNA	SHIMADZU	MCE-202	Microchip electrophoresis
MYOD1 (GFP-tagged)	ORIGENE	RG209108	Retroviral production
NanoDrop	Thermo Fisher	ND-ONE-W	Spectrophotometer
Nonessential amino acids	Thermo Fisher	11140-050	Cell culture
NucleoSpin Gel and PCR Clean-Up Kit	Clontech	740986.20	PCR clean up
NuPAGE 3-8% Tris-Acetate Protein Gels	Invitrogen	EA03785BOX	WB
NuPAGE Antioxidant	Invitrogen	NP0005	WB
NuPAGE LDS Sample Buffer	Invitrogen	NP0007	WB
NuPAGE Sample Reducing Agent	Invitrogen	NP0009	WB
NuPAGE Tris-Acetate SDS Running Buffer	Invitrogen	LA0041	WB
One Step TB Green PrimeScript RT-PCR Kit	TAKARA	RR066A	Titer check of retroviral vector
PBS	Thermo Fisher Scientific	14190-250	Cell culture
Pierce BCA Protein Assay Kit	Thermo Scientific	23227	WB
Polybrene Infection / Transfection Reagent	Sigma-Aldrich	TR-1003	Retroviral infection
pRetroX-TetOne-Puro Vector	Clontech	634307	Retroviral vecor
Puromycin	Clontech	631305	Cell culture
QIAGEN OneStep RT-PCR Kit	Qiagen	210212	PCR
REGM Bullet Kit	Lonza	CC-3190	Material for growth medium of UDCs
REGM SingleQuots	Lonza	CC-4127	Material for primary medium of UDCs
Retrovirus Titer Set	TAKARA	6166	Titer check of retroviral vector
Retro-X Concentrator	Clontech	631455	Retroviral production
RIPA buffer	Thermo Fisher Scientific	89901	WB
RNeasy kit	Qiagen	74104	RNA extraction for PCR
Tetracycline-free foetal bovine serum	Clontech	631106	Cell culture
Triton-X	MP Biomedicals	9002-93-1	ICC
Trypsin-EDTA (0.05%)	Gibco	25300054	Cell culture
XCell SureLock Mini-Cell	Invitrogen	EI0001	WB
Xfect transfection reagent	Clontech	631317	Transfection of plasmids into packaging cells