Assessing Stem Cell DNA Integrity for Cardiac Cell Therapy

Summary

Here, we provide a detailed description of an experimental setup for an analysis of the assessment of DNA integrity in stem cells prior to cell transplantation.

Abstract

Stem and stem-cell-derived cells have immense potential as a regenerative therapy for various degenerative diseases. DNA is the storehouse of genetic data in all cells, including stem cells, and its integrity is fundamental to its regenerative ability. Stem cells undergo rapid propagation in labs to achieve the necessary numbers for transplantation. Accelerated cell growth leads to the loss of DNA integrity by accumulated metabolites, such as reactive oxygen, carbonyl, and alkylating agents. Transplanting these cells would result in poor engraftment and regeneration of the deteriorating organ. Moreover, transplanting DNA-damaged cells leads to mutations, DNA instability, cellular senescence, and possibly, life-threatening diseases such as cancer. Therefore, there is an immediate need for a quality control method to evaluate the cell's suitability for transplantation. Here, we provide step-by-step protocols for the assessment of the DNA integrity of stem cells prior to cell transplantation.

Introduction

Experimental and clinical evidence demonstrates that cell transplantation can moderately improve the left ventricle contractile performance of failing hearts^{1,2,3,4,5,6,7,8,9}. Recent advances have opened further appealing opportunities for cardiovascular regeneration; these include the forced expression of reprogramming factors in somatic cells to induce pluripotency and differentiate these induced pluripotent stem cells (iPSC) into different cardiac lineages, importantly cardiomyocyte (CM)^10,11,12,13. The hereditary material in every cell, including the artificially generated iPSCs and iPSC-derived CM (iPS-CM), is DNA. The genetic instructions stored in DNA dictates the growth, development, and function of cells, tissues, organs, and organisms. DNA is not inert; cell metabolites, such as reactive oxygen, carbonyl, and nitrogen species, and alkylating agents can cause DNA damage in vitro and in vivo^14,15,16,17. Importantly, DNA damage occurs intuitively in every cell, with a significant frequency. If these damages are not corrected, it will lead to DNA mutation, cellular senescence, the loss of DNA and cell integrity, and possibly, diseases, including life-threatening cancers. Therefore, retaining DNA integrity is essential to any cell, especially iPSCs, that has enormous potential in the clinic.

For assessing the quantity and integrity of isolated genomic DNA, expensive equipment is available on the market. However, there are no simple and cost-effective methods to assess the DNA integrity in cells without isolating the cells. Moreover, user-induced DNA degradation during DNA isolation is one of the major drawbacks in using these methods. The single-cell gel electrophoresis (known as comet assay)^18,19 and γH2A.X immunolabeling⁸ techniques are fundamental approaches in research labs for assessing DNA damage. These two methods do not require expensive equipment or isolated genomic DNA to analyze DNA integrity^8,20,21. Since, these techniques have been performed with whole cells; user-induced DNA/RNA/protein degradation during the sample preparation will not affect these protocols. Here, to assess the DNA damage and DNA damage response in stem and stem-cell-derived cells, we provide step-by-step protocols to perform both the comet assay and γH2A.X immunolabeling. Moreover, combining these two approaches, we propose a naive assessment that can be used to evaluate the cell's suitability for transplantation.

The comet assay, or single-cell gel electrophoresis, measures the DNA breaks in cells. Cells embedded in low-melting agarose are lysed to form nucleoids containing supercoiled DNA. Upon electrophoresis, small pieces of fragmented DNA and broken DNA strands migrate through the agarose pores, whereas the intact DNA, due to their enormous size and their conjugation with the matrix protein, will have a restricted migration. The pattern of stained DNA under a fluorescence microscope mimics a comet. The comet head contains intact DNA and the tail is composed of fragments and broken DNA strands. The fraction of DNA damage can be measured by the fluorescence intensity of the damaged DNA (comet tail) relative to the intact DNA (comet head) intensity. The parameter tail moment can be calculated as shown in Figure 1.

DNA damage induces the phosphorylation of histone H2A.X (γH2A.X) at Ser139 by ATM, ATR, and DNA-PK kinases. The phosphorylation and recruitment of H2A.X at DNA strand breaks is called DNA damage response (DDR) and happens rapidly after DNA is damaged. Following this process, checkpoint-mediated cell cycle arrest and DNA repair processes are initiated. After the successful completion of DNA repair, γH2A.X is dephosphorylated and inactivated by phosphatases. Prolonged and multiple DNA strand breaks lead to the accumulation of γH2A.X foci in DNA. This indicates the cell's inability to repair the DNA damage and the loss of DNA integrity. These γH2A.X foci in DNA can be identified by and the number of DDR foci can be counted using the protocol in section 2.

Protocol

1. Comet Assay

1. Reagent preparation
   1. For low-melting-point agarose, place 500 mg of low-melting agarose in 100 mL of DNA-/RNA-free water. Heat the bottle in a microwave oven until the agarose dissolves. Place the bottle in a 37 °C water bath until needed.
      NOTE: For further reading, see Azqueta et al., who studied the effects of agarose concentration on the DNA-unwinding time and several electrophoresis factors²³.
   2. Dilute SYBR green DNA dye in Tris-EDTA (TE) Buffer at a 1:10,000 ratio to obtain a 1x working stock dye solution. This dye is light-sensitive, so store it in a dark place.
   3. For the cell lysis buffer, dissolve 100 mL of lysis buffer (2.5 M NaCl, 0.1 M EDTA, 10 mM Tris, 1% Triton X-100) in deionized water (DI H₂O). Then, add 10 M NaOH to adjust the pH to 10.0. Cool the buffer to 4 °C.
   4. For the alkaline DNA-unwinding/electrophoresis running buffer, dissolve 1 L of alkaline solution (0.3 M NaOH, 1 mM EDTA) in DI H₂O. Cool the buffer to 4 °C. Make sure the pH >13.
   5. For precoated comet slides, place a few drops of 0.5% agarose on a glass slide. Immediately, using the flat surface of another slide, spread the agarose to form a thin layer of agarose coating.
      NOTE: Dry the slides before using.
   6. For iPS cell culture, briefly culture iPS cells in basement-membrane-matrix-coated (see Table of Materials) culture plates in mTESR1 culture medium until confluency is reached.
      NOTE: Human-cardiac-fibroblast-derived iPS cells were used in this protocol. The reprogramming of iPS cell derivation and culture conditions is described in recent articles from our research group^12,13,21.
2. Sample preparation
   1. Discard the culture medium and wash the cells. Dissociate the cells using detachment solution (see Table of Materials). Wash the cell pellet with phosphate-buffered saline (PBS) and resuspend the cells in PBS at 1 x 10⁵ cells/mL.
3. Sample slide preparation
   NOTE: Perform the following steps under low-light conditions to avoid ultraviolet-light-induced cell damage.
   1. Mix 10 μL of cell suspension and 90 μL of agarose solution (1:10 ratio) in a tube. Place the tube in a 37 °C water bath to prevent the agarose from solidifying.
   2. Mix the solutions without introducing air bubbles and pipette 70 μL/spot onto the precoated comet slide. Using a pipette tip, spread the cell agarose mixture to form a thin layer. Place the slide in 4 °C for 15 min.
   3. In a container, completely submerge the slide in cold lysis buffer. Place the container in the dark at 4 °C for 1 h.
   4. Replace the lysis buffer with cold alkaline solution. Make sure the slides are completely submerged. Place the container in the dark at 4 °C for 30 min.
4. Electrophoresis
   1. Place the slide in a horizontal electrophoresis tank. Fill the tank with cold alkaline electrophoresis buffer until the slides are completely submerged. Apply voltage at 1 V/cm for 15 to 30 min.
      NOTE: Total voltage = distance between the electrodes x 1 V
   2. In a container, completely submerge the slide in cold DI H₂O. After 2 min, remove the DI H₂O and add fresh DI H₂O. Repeat this step.
   3. Replace the DI H₂O with cold 70% ethanol. Wait 5 min. Gently remove the slide, do not tilt it, and let it air-dry.
   4. Once dried, add 100 μL of diluted DNA dye to each spot. Wait 15 min at room temperature. Using a FITC filter in an epifluorescence microscope, take images of 50 to 100 comets in total per sample.
5. Image analysis and calculation of the results
   1. For scoring the comets, use the National Institutes of Health’s (NIH) ImageJ with comet assay plugin (download ImageJ here: https://imagej.nih.gov/ij/download.html; download the plugin here: https://www.med.unc.edu/microscopy/resources/imagej-plugins-and-macros/comet-assay/).
      NOTE: The plugin comes with a PDF instruction which contains all details to perform the analysis. Additionally, screenshots of the comet analysis are shown in Figure 2A-C. Representative comet images of control and doxorubicin (Doxo)-treated iPS cells and the quantification of the comets are shown in Figure 3A-C.

2. DNA Damage Response

1. Sample and reagent preparation
   1. For an iPS-CM cell culture, culture iPS-CM cells in basement-membrane-matrix-coated (see Table of Materials) culture plates in RPMI medium supplemented with B-27 (CMM) until confluency is reached.
      NOTE: Human-iPS-cell-derived cardiomyocytes were used in this protocol. The protocol for iPS cell differentiation into cardiomyocytes can be found in recent articles from our research group^12,13,21.
   2. Seed iPS-CMs in chamber slides.
      1. Discard the culture medium from the iPS-CM wells. Wash the cells three times with PBS.
      2. Add 1 mL of 0.25% trypsin per well and incubate at 37 °C for 5 min. Check the plate under a microscope for cell detachment. Add 1 mL of CMM to stop the trypsin.
      3. Place cell suspension in a 15 mL tube and centrifuge for 5 min at 4 °C and 200 x g. Discard the medium, add 1 mL of CMM, and resuspend the cells. Count the cells and adjust the cell count to obtain 20 x 10⁵ cells in 1.6 mL of CMM.
      4. Seed 200 µL of cell suspension per well of the 8-well chamber slide (see Table of Materials). Tap the slide gently to spread the cells around the well and incubate at 37 °C.
   3. For the iPS-CM doxorubicin treatment, discard the culture medium from the iPS-CM wells. Wash the cells with PBS. Treat the cells with 1 μM doxorubicin and CMM for 4 h. Aspirate the medium and wash the cells with PBS.
   4. For the blocking buffer, prepare 10 mL of bovine serum albumin (BSA) solution containing 3% BSA and 0.05% Triton X-100. To prepare 10 mL of blocking buffer, add 1 mL of normal donkey serum to 9 mL of prepared BSA solution.
   5. For the primary antibody solution, add 1 μL of anti-rabbit phospho-histone H2A.X (Ser139) antibody to 200 μL of blocking buffer.
   6. For the secondary antibody mix, add 1 μL each of fluorochrome-conjugated anti-rabbit secondary antibody, DAPI, and fluorochrome-conjugated phalloidin to 200 μL of blocking buffer.
2. Immunolabeling
   1. Wash the cells three times with PBS and add 200 μL of freshly prepared 4% paraformaldehyde (PFA) to each well. Fix the cells for 20 min in the dark at room temperature. Wash the cells with PBS.
   2. Remove the PBS and add 200 μL of blocking buffer per well and block for 30 min in a humidified chamber at room temperature. Remove the blocking buffer and add 200 μL of primary antibody solution. Incubate for 45 min in a dark, humidified chamber at room temperature. Then, wash the wells three times with PBS.
   3. Remove the PBS and add 200 μL of secondary antibody mix. Incubate for 45 min in a dark, humidified chamber at room temperature. Then, wash the wells three times with PBS. Wash with DI H₂O before mounting them with antifade. Place a coverglass and store the slides in the dark at 4 °C.
   4. Using an epifluorescence microscope, take three to five images of random fields per sample, as shown in Figure 4A, and proceed to image analysis.
3. Counting of the DDR foci
   1. Download and install CellProfiler²⁴ (http://cellprofiler.org).
   2. NOTE: Image processing in this study was performed using CellProfiler version 2.1.1. Tutorials for CellProfiler that were used can be found elsewhere (https://www.youtube.com/watch?v=PvhRL9xpduk&list=PL7CC87670239B4D10). If a newer version of CellProfiler is being used, the pipeline might require minor adaptations.
   3. Download the pipeline punctae_gH2AX.cpipe. Select File > Import > Pipeline from the file and choose punctae_gH2AX.cpipe.
   4. Drag-and-drop the folder containing the acquired images of γH2A.X foci to the File list window in the Input modules/Images section for analysis (Figure 5A). Then, follow the instructions as shown in Figure 5A-L.
   5. Set the following parameters for the images:
      1. Drag the desired image for analysis onto the File list. Under Input modules, select Images (see Figure 5A for module settings). In Input modules, select Metadata (see Figure 5B for module settings). In Input modules, select NamesAndTypes (see Figure 5C for module settings).
      2. For Groups, select no. In Analysis modules, select ColorToGray (see Figure 5D for module settings).
   6. In Analysis modules, select Smooth (see Figure 5E for module settings).
      NOTE: This value may need to be optimized, depending on the image resolution.
   7. In Analysis modules, select IdentifyPrimaryObjects (see Figure 5F for module settings).
      NOTE: Optimize these values to make sure the whole nucleus is selected. After this step, the computer may lag.
   8. In Analysis modules, select Smooth (see Figure 5G for module settings).
      NOTE: This value may need to be optimized, depending on the image resolution.
   9. In Analysis modules, select EnhanceOrSuppressFeatures (see Figure 5H for module settings).
   10. In Analysis modules, select IdentifyPrimaryObjects (see Figure 5I for module settings).
       NOTE: Optimize these values to make sure the punctae are selected. After this step, the computer may lag again.
       1. In Analysis modules, select RelateObjects (see Figure 5J for module settings). In Analysis modules, select ClassifyObjects (see Figure 5K for module settings). In Analysis modules, select ExportToSpreadsheet (see Figure 5L for module settings).
       2. Click Analyze Images at the bottom left panel to perform image analysis. At the successful completion of the analysis, several images are generated (Figure 6A-F).
          NOTE: Users should save these images for future reference.
       3. Note the .csv file containing the quantitative data for further analysis that is generated and saved in the appropriate location on the computer. In the spreadsheet called MyExpt_Image, columns B and D will have the number of nuclei that have up to five and more punctae, respectively. Add columns B and D to get the total number of nuclei.
   11. Repeat step 2.3.3 - 2.3.8 for all images (change the MyExpt_ filename before every analysis). Plots can be made for assessing DNA integrity, as shown in Figure 4C.

Results

Human induced pluripotent stem cells were cultured, and the DNA damage and the tail moment, which were used as a measure of DNA integrity, were analyzed by comet assay. iPS cells were embedded in low-melting-point agarose and placed on a glass slide. The cells were, then, treated with lysis buffer, followed by an alkaline solution, to obtain supercoiled DNA. Nucleoids were electrophoresed and comets were visualized by DNA dye (Figure 1A-D). T...

Discussion

DNA integrity portrays cell integrity. Cells with damaged DNA are frequently in stress and eventually lose their integrity. The integrity of stem and stem-cell-derived cells that are being propagated for the purpose of transplantation is principal for the cells to perform their desired function. Transplanting cells with damaged DNA would result in a poor engraftment rate and performance of the cell^8,20. Therefore, examining the DNA integrity prior to cell transpl...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
0.25% Trypsin	Corning	25200056
8-well chamber slide	Millicell	PEZGS0816
Accutase	Stemcell Technologies	7920	Cell detachment solution
Alexa Fluor 488 AffiniPure Donkey Anti-Rabbit IgG	Jackson Immuno Research Laboratories	711-545-152 (RRID: AB_2313584)
Bovine Serum Albumin	Sigma-Aldrich	A7906
Cy3 AffiniPure Donkey Anti-Rabbit IgG	Jackson Immuno Research Laboratories	711-165-152 (RRID:AB_2307443)
DAPI	Sigma-Aldrich	D9564
Gibco B-27 Supplement, Serum Free,	Gibco	17504-044
Matrigel growth factor reduced	Corning	354230
mTeSR1	Stemcell Technologies	85850
PhalloidinA488	Life Technology	A12379
Phospho-Histone H2A.X (Ser139) Antibody	Cell Signaling Technology	2577 (RRID: AB_2118010)
RPMI	Gibco	11875-093
SYBR Green I nucleic acid gel stain	Sigma-Aldrich	S9430
Triton X-100	Fisher scientific	BP151-100
UltraPure Low melting Point Agarose	Invitrogen	16520050
Vectashield	Vector Laboratories	H-1000	Antifade