JHvB is supported by grants from the NIH, Regenerative Medicine Minnesota, and an individual Biomedical Research Award from The Hartwell Foundation.

All animal experiments were performed conform the National Institutes of Health guidelines and approved by the University of Minnesota Institutional Animal Care and Use Committee (IACUC).
1. Preparation of the solutions and surgical equipment
<ol>
	<li>Prior to isolation, sterilize the surgical equipment by using 70% ethanol solution.</li>
	<li>Add 2.24 g of KCl to 500 mL phosphate buffered saline (PBS) solution to obtain a final concentration of 60 mM. Store KCl-PBS solution at room temperature. Use 3 mL of KCl-PBS solution per mouse.</li>
	<li>Dilute 32% paraformaldehyde (PFA) solution with PBS into to obtain final concentration of 4% PFA. Prepare 10 mL of 4% PFA in PBS per mouse. Diluted PFA solution can be stored at 4 &#176;C for 2-3 weeks in a glass container. 
	NOTE: Prepared 4% PFA solution can be stored at -20 &#176;C for longer periods of time.</li>
	<li>Prepare 1 mL of collagenase solution per mouse by adding 60 mg of collagenase, type 2 per 1 mL of PBS.</li>
</ol>
2. Perfusion and fixation of the heart
<ol>
	<li>Anesthetize the animal by using 2-5% isoflurane with an oxygen flow rate of 1 L/min. Confirm the anesthesia by confirming lack of movement and lower rate of breathing. 
	NOTE: Injecting heparin (100-500 U/kg) before euthanasia can increase the cell quality and yield by preventing blood clots, thereby allowing for more efficient perfusion of the heart with fixative.</li>
	<li>Euthanize the animal according to approved methodologies. 
	NOTE: We followed the American Veterinary Medical Association guidelines for the euthanasia of animals, and obtained local IACUC approval for euthanasia.</li>
	<li>Place the euthanized animal in supine position, and tape down extended limbs.</li>
	<li>Cut through the chest to expose the heart using blunt-end scissors. Cut descending aorta and inferior caval vein.</li>
	<li>Perfuse the heart by injecting 3 mL of KCl-PBS solution through the left ventricle with a flow rate of 3 mL/min using a peristaltic pump attached to an infusion set with a 23 G butterfly needle (26 G for neonates). Make sure not to pierce through the septum. 
	NOTE: Alternatively, use a needle attached to a syringe to inject solutions.</li>
	<li>Perfuse the heart by injecting 10 mL of 4% PFA solution for 10 min using a peristaltic pump at a rate of 1 mL/min.</li>
	<li>Remove the whole heart using scissors. After removing the heart, it is possible to isolate a specific region of the heart by incising. Place the heart, or a segment of it in a 1.5 mL microcentrifuge tube containing 1 mL of 4% PFA solution. Incubate the heart on rocker at room temperature with rocking speed between 20-30 rpm for 1 h.</li>
</ol>
3. Isolation of fixed cardiomyocytes
<ol>
	<li>Place the heart in a Petri dish containing PBS solution. Squeeze the heart to get rid of any PFA remaining in ventricles, and wash in PBS.</li>
	<li>Put the fixed heart into a new 1.5 mL microcentrifuge tube containing collagenase solution (60 mg/mL). Place the tube on rocker (20-30 rpm) at 37 &#176;C for overnight incubation. 
	NOTE: Extend the incubation time up to 1 week and replenish the collagenase solution every two days to reduce the possible variation in yield if hearts are anticipated to be fibrotic, which might require longer time of collagenase digestion to digest extracellular collagen.</li>
	<li>Put collagenase solution and the heart into a 35 mm Petri dish. Dissociate the heart into 1 mm pieces by using forceps or scissors.</li>
	<li>Use a transfer pipette to further triturate the dissociated tissue for 2 min. If tissue particles still remain in the dish, use a transfer pipette with narrower opening and continue trituration. Continue until the majority of the tissue is broken down. 
	NOTE: Over trituration causes individual cardiomyocytes to break. Make sure not to over triturate by checking regularly under a microscope.</li>
	<li>Place a 200-600 &#181;m nylon mesh over opening of 15 mL centrifuge tube. 
	NOTE: For hypertrophied cardiomyocytes, it is recommended to use 400 &#181;m nylon mesh instead of 200 &#181;m.</li>
	<li>Add 5 mL of PBS to the Petri dish containing dissociated cells and filter the solution through nylon mesh, including tissue particles. Wash the nylon mesh by passing additional 4 mL PBS.</li>
	<li>Centrifuge the filtered solution at 10-100 x g for 1 min. 
	NOTE: 100 x g centrifugation will not yield 100% pure cardiomyocyte population, and some non-cardiomyocyte cells are likely to be included.</li>
	<li>Discard the supernatant unless one wants to stain/evaluate non-cardiomyocytes cardiac cells as well. Resuspend the pellet in 10 mL PBS prior to staining.</li>
</ol>
4. Staining cardiomyocytes
<ol>
	<li>Collect the cells by centrifugation at 100 x g for 1 min and add 5 mL of permeabilization solution (e.g., 0.5% Triton X-100 in PBS). Incubate for 20 min at room temperature on rocker. 
	NOTE: For steps 4.1, 4.2 and 4.4 use 15 mL centrifuge tubes as it is easier to remove the supernatant without disturbing the cell pellet compared to 1.5 mL microcentrifuge tubes.</li>
	<li>Collect the cells by centrifugation at 100 x g for 1 min, add 5 mL of blocking buffer (e.g., 3% bovine serum albumin [BSA] in PBS) and incubate for 30 min at room temperature on a rocker.</li>
	<li>Collect the cells by centrifugation at 100 x g for 1 min and add 1 mL of primary antibody solution (in PBS) with the appropriate dilution ratio. Transfer the solution into 1.5 mL microcentrifuge tube and incubate cardiomyocytes in primary antibody solution under optimized conditions (e.g., 4 &#176;C overnight).</li>
	<li>Transfer cardiomyocytes with primary antibody solution to a 15 mL centrifuge tube and add 9 mL of PBS. Incubate the cardiomyocytes for 10 min at room temperature on a rocker.</li>
	<li>Collect the cells by centrifugation at 100 x g for 1 min and add 10 mL of PBS. Incubate the cardiomyocytes for 10 min at room temperature on a rocker. Repeat this step once more.</li>
	<li>Collect the cells by centrifugation at 100 x g for 1 min and add the secondary antibody solution containing DAPI. Incubate for 30 min at room temperature on a rocker, followed by repeating step 4.5 twice to wash cardiomyocytes.</li>
	<li>Place the cells either on coverslips or microscope-compatible plates and proceed with imaging. 
	NOTE: Images included in the manuscript were taken with 10x and 40x objectives. Lasers used were: 405 nm for DAPI, 561 nm for Alpha actinin and 640 nm for Edu.</li>
</ol>
5. Setup imaging software
NOTE: Follow along with these steps using Supplementary File 1-SoftwareScreenshots.pdf.
<ol>
	<li>Download the Fiji distribution of ImageJ.</li>
	<li>Open Fiji. Click on Help &#62; Update&#8230; &#62; Manage Update Sites. Check the &#34;IJPB-plugins&#34; and &#34;Biomedgroup&#34; update sites to download the dependencies plugins Ellipse Split and Morpholibj.</li>
	<li>Click Close. Fiji should begin downloading the dependencies. Restart Fiji when finished.</li>
	<li>Download Rstudio and open it.</li>
	<li>Copy install.packages(c(&#34;ggplot2&#34;, &#34;autothresholdr&#34;, &#34;dplyr&#34;, &#34;purrr&#34;, &#34;jsonlite&#34;, &#34;shiny&#34;)) into R console&#39;s command line and press the Enter key. Type &#34;y&#34; in response to all prompts to install all R dependencies (Screenshot 1 in Supplementary File 1).</li>
</ol>
6. Image quantification
<ol>
	<li>Open Fiji and drag &#34;AnalyzeNucleation.py&#34; (supplied as a supplementary code file) into Fiji&#39;s status bar. This will open a script-editing window. Click Run in the lower left corner to begin it (Screenshot 2 in Supplementary File 1).</li>
	<li>A dialog box will pop up (Supplementary File 1: Screenshot 3), asking for the location of the output data directory. All analysis data, figures, and other data used by this software will be stored in this folder. Another, larger dialog box will pop up, displaying all image analysis settings (Supplementary File 1: Screenshot 4).
	<ol>
		<li>Select location of directory containing images to be analyzed.</li>
		<li>Enter the image filename format using regular expressions. Enter the image filename format, indicating which parts of the filename correspond to row, column, channel, and (optionally) site within braces, using regular expressions. Do not put spaces within the braces. Surround variable parts of the filename format in braces {}. The way files are saved depends on the imaging software, and this step will retrieve relevant information from the image filename. 
		NOTE: For example, the format string 
		r&#34; Plate 1-(?P&#60;row&#62;[A-Za-z]+)(?P&#60;column&#62;[0-9]+)-(?P&#60;channel&#62;[A-Za-z]+).tif&#34; 
		describes a filename that starts with &#34;Plate 1-&#34;, which is followed by one or more alphabetical letters indicating the row, which is followed by one or more digits indicating the column, which is followed by &#34;-&#34;, which is followed by one or more letters indicating the channel, which is followed by &#34;.tif&#34;. The letters inside the angle brackets like &#34;&#60;&#62;&#34; are variable names and are automatically copied into the data when it is collected. One of the variable names must be &#34;&#60;channel&#62;&#34;</li>
		<li>Indicate the name of channels in which the nuclear stain is visible and where the cardiomyocytes are visible. These names must be exactly as they are in the part matched by the &#34;&#60;channel&#62;&#34; variable in the regular expression filenames.</li>
		<li>Indicate how the images should be grouped using comma-separated variable names. All of the images within a given group will be opened and analyzed in one batch. For example, if the images are divided into sets for each well, and there is a well for each unique combination of row and column, then write &#34;row, column&#34; in this field. 
		NOTE: These grouping variables must be a subset of the variables used in the format string. Do not use &#34;channel&#34; as a grouping variable, this will separate corresponding channel images from each other.</li>
		<li>Indicate whether or not images are stitched together in one well image or are separate for each site. In the former case, site should not be indicated in the filename format string.</li>
		<li>Choose which thresholding method to use to separate nuclei from the background. All of Fiji&#39;s standard thresholding methods are available. Test different thresholding methods to determine which works best for the image set. In this example, choose the Otsu method.</li>
		<li>Indicate whether or not the threshold should be recalculated for each site image or if the same threshold should be used for every image in the group. Indicate whether the cardiomyocyte images are brightfield or use a fluorescent marker.</li>
		<li>Indicate the cardiomyocyte thresholding method. If brightfield was chosen in the previous step, this thresholding method will be applied to edge-filtered brightfield images. Indicate whether or not the threshold should be recalculated for each site image or if the same threshold should be used for every image in the group.</li>
		<li>Indicate the number of rows of site images that cover each well. Indicate the number of columns of site images that cover each well. Indicate the minimum area of nuclei in pixels. Use a generously low minimum size, a higher and more precise threshold will be calculated in the analysis step. Indicate the minimum area of cardiomyocytes.</li>
		<li>After choosing the desired settings click OK.</li>
	</ol>
	</li>
	<li>Images resembling those found in Figure 3 and Figure 4 will appear on the screen, showing the different stages of the analysis pipeline. Inspect these images to ensure that thresholding and segmentation are occurring properly.</li>
	<li>The selected results folder should now be filled with analysis data (Supplementary File 1: Screenshot 5). Files other than analysis data can safely be saved in this folder as long as their names do not begin with &#34;cm_&#34;, &#34;nuclei_&#34;, or &#34;nucleilink_&#34;.</li>
</ol>
7. Data analysis
NOTE: The csv files that are produced can be analyzed manually. Each analyzed image subset produces a triplet of csv files named &#34;nuclei(metadata).csv&#34;, &#34;nucleilink(metadata).csv&#34;, and &#34;cardiomyocytes(metadata),csv&#34;, where (metadata) is replaced with a sequence of name-value pairs of the form &#34;_(name)=(value)&#34;, where (name) and (value) are sequences of alphanumeric characters derived from strings matched in the regular expression given earlier. (For example, if row and column were indicated in the filenames then strings like &#34;_row=F&#34; and &#34;_column=8&#34; will be present). The unnamed leftmost column of each nuclei and nucleilink file is a nucleus ID number. The &#34;Min&#34; column of the nucleilink file is the id of the cardiomyocyte that contained said nucleus wholly or 0 otherwise. The &#34;Max&#34; column of the nuclei is the ID of the highest-numbered cardiomyocyte that contained said nucleus in part, or 0 otherwise. The &#34;Mean&#34; column of the cardiomyocytes file is the cardiomyocyte id number.
<ol>
	<li>Open &#34;AnalyzeMultinucleatedServer.R&#34; in Rstudio (provided as supplementary code file).</li>
	<li>At the top of this file is a variable named &#34;folderName&#34;. Next to it is a filepath. In here, type the path to the output data folder selected in the last step, without the final slash (Supplementary File 1: Screenshot 6).</li>
	<li>In the upper left corner of the script editing window there should be a green arrow labeled Run App. Click this arrow. It may take some time for the data to load and for the app to pop up.</li>
	<li>Initially, three gating graphs will be visible, one to indicate the minimum valid nuclear area threshold, one to indicate the minimum valid nuclear mean intensity threshold, and one to indicate the maximum valid minimum feret&#39;s diameter for cardiomyocytes. Use the sliders to set these thresholds (Supplementary File 1: Screenshot 7). 
	NOTE: In each of these graphs, a large, broad peak corresponding to valid nuclei or cardiomyocytes should be present, flanked by broad tails representing debris or erroneous segmented cardiomyocytes. Use the thresholds to cut one tail of each of the peaks off.</li>
	<li>Scroll down. Click the button Apply Selected Thresholds (bottom of Supplementary File 1: Screenshot 7).</li>
	<li>Click the button Plot Intensity Distribution. This will render plot of the nuclear intensity distribution of both the entire sample and separate subplots for each grouping variable. 
	NOTE: For example, if &#60;row&#62; and &#60;column&#62; grouping variables were entered into the regular expression in the Fiji dialog, plots indicating the intensity distribution by row and by column will appear here (Supplementary File 1: Screenshot 8). If illumination and staining conditions were constant across the different parts of the sample, these plots should all clearly show two intensity peaks, a dimmer, taller one for the diploid nuclei and a brighter, shorter one for the tetraploid nuclei.</li>
	<li>Intrasample variation will result in this pattern not being visible in the whole-sample plot and there being great variety in the location of the diploid and tetraploid peaks by row, column, or other grouping variable. In the latter case, scroll down check the checkbox Normalize Separately by group to account for this variation (Supplementary File 1: Screenshot 9).</li>
	<li>Click the button Calculate Ploidy (Supplementary File 1: Screenshot 9). Click the button Plot Estimated Ploidy Distribution. Graphs will appear in the empty windows to the right. In the normalized whole-sample graph, the two-peak pattern should be visible if it wasn&#39;t before.</li>
	<li>Select thresholds to isolate the diploid and tetraploid peaks from both each other and outliers using the sliders (Supplementary File 1: Screenshot 9). Scroll down. Click the button Calculate Ploidy and Nucleation (Supplementary File 1: Screenshot 10).</li>
	<li>Click the button Plot and Save Into Results Folder. The plot saved into the selected results folder will also appear in this interactive window (Supplementary File 1: Screenshot 10).</li>
</ol>

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The authors have nothing to disclose.

Since cardiomyocytes cannot be maintained in culture, it is important to isolate primary cardiomyocytes to be able to study their architecture and function11. Hence, cardiomyocyte isolation techniques have been widely used in the cardiac field. If the goal is to determine functional aspects of cardiomyocytes, it is important to isolate viable cardiomyocytes. These live cardiomyocytes can also be used to perform immunostaining on isolated cardiomyocytes. However, optimizing the technique of isolating live cardiomyocytes is technically challenging, and even the best techniques typically only yield 60-65% live rod-shaped cardiomyocytes, and the remaining cardiomyocytes are all balled up and dying or dead11,12. Here, we developed a technique that will allow researchers to first fix the heart, and then isolate cardiomyocytes efficiently. This new protocol allows for much higher yields of rod-shaped cardiomyocytes compared to previously published protocols. Furthermore, we developed an imaging analysis platform to categorize cardiomyocytes automatically based on nucleation and ploidy. With these new methodologies, groups can stain cardiomyocytes for different proteins, and study cardiomyocyte ploidy and nucleation status as surrogates for the regenerative potential of the heart.
The protocol described here is relatively straightforward, and can be performed without any advanced equipment. The amount of collagenase and incubation time for digestion might vary depending on the collagenase lot, and the company providing it. We used collagenase type 2, since this is most widely used to digest the heart for obtaining live cardiomyocytes. Based on our observations, we determined that overnight incubation with 60 mg/mL collagenase type 2 is optimal for almost all mouse hearts regardless of the level of fibrosis. We have never had an issue of overdigestion as intracellular proteins are fixed and not as accessible as extracellular collagen. However, if the heart is not digested properly, more vigorous trituration might be needed, which causes cell fragmentation due to shear stress. Thus, it is crucial to make sure that the heart is digested properly before moving on to trituration. Stiffness of the heart can be tested by squeezing with forceps to assess the degree of digestion. Following incubation with collagenase, hearts should be less stiff and easy to tear apart. Other types of collagenase can also be used. A previous report used a combination of collagenases B and D14.
Furthermore, we believe that this protocol can be used to assess overall number of cardiomyocytes in the heart15. However, if the goal is to obtain and quantify all cardiomyocytes from the heart, it is important to incubate the hearts for extended periods of time in the collagenase solution (e.g., 3-7 days), where the collagenase solution should be replenished once a day. This will minimize inconsistencies in isolation efficiency by eliminating the impact of the degree of trituration on cardiomyocyte yield.
The use of DNA content to measure ploidy is not new, and has been used in flow cytometry for decades. Recently, it was shown that microscopy can similarly be used to estimate DNA content per nucleus16. Here, we implemented this strategy to measure ploidy of cardiomyocyte nuclei, as a surrogate for newly formed cardiomyocytes. The dogma in the field of cardiac regeneration is that only mononucleated, diploid cardiomyocytes can undergo cytokinesis and give rise to new cardiomyocytes. Since it is very challenging to measure new cardiomyocyte formation in vivo, isolating cardiomyocytes that have been chased after administration of a DNA nucleotide analog and determining the level of mononucleated, diploid cardiomyocytes has been used as an approximation of the ability of the heart to generate new cardiomyocytes17. Here, we provide a macro for ImageJ that allows easy quantification of cardiomyocyte ploidy. At the very minimum, 500 nuclei must be measured to attain an accurate estimate of the location of the G1 peak. If care is taken to ensure that staining and imaging conditions are consistent across every well of the imaged plate, only 500 nuclei across the entire sample need to be imaged, otherwise, there need to be 500 nuclei per image group18,19. Limitations of imaging-based measurement of nucleation and ploidy include difficulty to distinguish nuclei from adherent cells from actual cardiomyocyte nuclei, when using two-dimensional images. Such adherent cells might result in overestimation of the quantity of multinucleated cells and decrease the accuracy of measurements of the tetraploid cardiomyocyte nucleus population. One possible strategy to solve this problem would be to use the cardiomyocyte nuclear marker PCM16,20. However, we have had difficulties to obtain reliable PCM1 staining on properly fixed cells or tissues.
Another potential limitation is that some nuclear stain images might have significant background cytoplasmic staining, preventing proper thresholding using Fiji&#39;s built in methods without extensive preprocessing. In addition, the irregular contribution of this background fluorescence into ploidy estimates reduces their accuracy. Moreover, if the cells are not left in DNA-staining solution for sufficient time, the fluorescent dye will not bind to saturation within the nuclei and the assumption of a linear relationship between nuclear integrated intensity and DNA content will no longer be accurate.
It should be noted that the software cannot segment cardiomyocyte clusters and instead removes them from analysis. Therefore, it is critically important to seed cardiomyocytes at a relatively low density (e.g., 1000 cells/cm2). Further, the software cannot distinguish between two cardiomyocytes lined up end-to-end and long, singular cardiomyocytes. These sorts of clusters might erroneously inflate multinucleation estimates.
Although the described method does not allow for obtaining viable cardiomyocytes and thus cannot be used to measure dynamic cellular processes, if the goal is to perform immunostaining, we believe that the described method is superior to existing protocols with higher yields of cardiomyocytes and better quality in terms of morphology and protein localization. Finally, the described method could be used to isolate cardiomyocytes from clinical samples14,21. We believe the described methodology can help different researchers to obtain high-quality cardiomyocytes and measure nucleation and ploidy as surrogates for new cardiomyocyte formation.

Heart disease has been the leading cause of death in the majority of western countries for many decades1,2. Although many improvements in the treatment of cardiovascular diseases have improved survival, there are currently no treatments that can replace lost cardiomyocytes. Therefore, studies related to cardiomyocyte function, proliferation, apoptosis and hypertrophy have been and continue to be a major focus of the scientific community. Since the adult mammalian heart has a very limited regenerative capacity, with an estimated cardiomyocyte renewal rate of less than 1% per year, it is crucially important to reliably identify cardiomyocyte proliferative events3,4. Most strategies that measure proliferative events rely either on staining for incorporated DNA nucleotide analogs to assess previous or current proliferation, or stain for nuclear markers of active proliferation5. It is especially important to reliably identify cardiomyocyte proliferative events since the overall number of proliferative cardiomyocytes is so low3,6. For example, based on a 1% renewal rate of endogenous cardiomyocytes per year, one can expect to find between 25 and 50 cardiomyocytes to be proliferative at any given time in the adult mouse heart7,8. Any inaccuracies in identification of cardiomyocyte nuclei might lead to false positive results. Therefore, it is critical to reliably identify cardiomyocyte nuclei, which has proven difficult and unreliable from histological sections9. Identification of cardiomyocytes is much more accurate from single cells than from tissue sections as it might be difficult to distinguish cardiomyocytes from other cell types even when using markers such as &#945;-actinin, although PCM1 might be a reliable marker of cardiomyocyte nuclei in histological sections10.
Current protocols rely on isolating live cardiomyocytes prior to fixation, which is known to cause death of at least 30% of cardiomyocytes, and might lead to inadvertent selection of specific populations of cardiomyocytes11. Furthermore, these protocols are notoriously difficult to optimize to provide reproducible results. Even optimized isolation techniques can typically produce no more than 65% live, rod-shaped cardiomyocytes with varying yields12.
To overcome these issues, we developed a protocol that allows researchers to isolate fixed cardiomyocytes. Since the samples are fixed prior to isolation, the yield is maximized, and in vivo morphology is well preserved. Moreover, with this protocol it is possible to isolate cardiomyocytes from clinical samples, which are typically fixed immediately after procurement. Furthermore, to identify newly generated cardiomyocytes, it is important to measure the nucleation and ploidy status of individual cardiomyocytes, since only diploid cardiomyocytes are typically assumed to be newly formed. Flow cytometry cannot distinguish multinucleation from polyploidy and is a relatively time and resource-intensive protocol. Manual outlining and measurement of nuclei within images is very low-throughput and prone to human bias. Automated quantification of images of fixed, isolated DAPI-stained cardiomyocytes solves both of these problems. Imaging-based determination of nucleation and ploidy distributions can be obtained with a minimum of time and reagents using basic equipment.

<table><tbody><tr><td>96 wells plate for imaging</td><td>Corning</td><td>3340</td><td>We use these plates as they are suitable for imaging, although glass bottom plates would be better for confocal imaging</td></tr><tr><td>Alpha actinin</td><td>Novus Biologicals</td><td>NBP1-32462</td><td>This antibody is used as a marker of cardiomyocyte sarcomeres</td></tr><tr><td>Blunt scissors</td><td>Fine Scissor Tools</td><td>14072-10</td><td>We prefer blunt scissors as the possibility of tearing heart tissue is lower when exposing the heart</td></tr><tr><td>C57BL/6J</td><td>The Jackson Laboratory</td><td>664</td><td>Used for imaging, assessing ploidy and nucleation in cardiomyocyte population</td></tr><tr><td>CD-1 mice</td><td>Charles river</td><td>22</td><td>Used for imaging, assessing ploidy and nucleation in cardiomyocyte population</td></tr><tr><td>Collagenase 2</td><td>Worthington</td><td>LS004177</td><td>For the purpose of this protocol, the batch to batch differences are minimal and don&#039;t affect overall yield and quality of the isolation</td></tr><tr><td>Copper (II) sulfate pentahydrate</td><td>Sigma-Aldrich</td><td>203165-10G</td><td>For edu staining</td></tr><tr><td>Cy5 Picolyl Azide</td><td>Click Chemistry Tools</td><td>1177-25</td><td>Azide used for edu staining</td></tr><tr><td>Cytation3</td><td>BioTek</td><td>-</td><td>Used for automated imaging for DNA analysis</td></tr><tr><td>DAPI</td><td>Life Technologies</td><td>D3571</td><td>DAPI used for DNA staining. Stocks were dissolved in distilled water.</td></tr><tr><td>donkey anti-mouse IgG-Alexa568</td><td>Life Technologies</td><td>A10037</td><td>Secondary antibody used to detect alpha actinin staining within cardiomyocytes</td></tr><tr><td>Forceps</td><td>ROBOZ</td><td>RS-5137</td><td>We use these curved, blunt forceps, although straight forceps could also be used</td></tr><tr><td>Hydrochloric acid</td><td>Fisher Scientific</td><td>A144212</td><td>To set pH of Tris-HCl buffer to pH 8.5</td></tr><tr><td>ImageJ</td><td>&lt;a href=&quot;https://imagej.net/Fiji/Downloads&quot;&gt;imagej.net/Fiji/Downloads&lt;/a&gt;</td><td>-</td><td>Used for analyzing images</td></tr><tr><td>L-ascorbic acid</td><td>Sigma-Aldrich</td><td>255564-100G</td><td>For edu staining</td></tr><tr><td>Needle for infusion</td><td>TERUMO</td><td>SV*23BLK</td><td>We use winged infusion sets throughout the protocol as it is easy to manipulate the position of the needle with these sets during injection</td></tr><tr><td>Nikon A1R HD25</td><td>Nikon</td><td>-</td><td>Used to take confocal images of alpha actinin staining</td></tr><tr><td>Nylon mesh 200 micron</td><td>Elko filtering</td><td>03-200/54</td><td>Mesh used for filtering regular cardiomyocytes (not hypertrophied)</td></tr><tr><td>Nylon mesh 400 micron</td><td>Elko filtering</td><td>06-400/38</td><td>Mesh used for filtering hypertrophied adult cardiomyocytes</td></tr><tr><td>Phosphate Buffered Saline (1X)</td><td>Corning</td><td>21-040-CV</td><td>This can also be prepared in the lab. Although sterility is important in this experiment, we think it is sufficient to prepare PBS and filtering it</td></tr><tr><td>Potassium chloride, Granular</td><td>Mallinckrodt</td><td>6858</td><td>Granular potassium chloride was preffered by us as it forms less aggregates when stored in room temperature</td></tr><tr><td>R</td><td>&lt;a href=&quot;http://www.r-project.org/&quot;&gt;r-project.org&lt;/a&gt;</td><td>-</td><td>Used for data analysis of the measurements obtained from images</td></tr><tr><td>Tris Base</td><td>Fisher Scientific</td><td>BP152-5</td><td>Used to buffer EdU staining reaction</td></tr></tbody></table>

isolation of cardiomyocytes from fixed hearts for immunocytochemistry and ploidy analysis

The adult mammalian heart is composed of various cell types including cardiomyocytes, endothelial cells and fibroblasts. Since it is difficult to reliably identify nuclei of cardiomyocytes on histological sections, many groups rely on isolating viable cardiomyocytes prior to fixation to perform immunostaining. However, these live cardiomyocyte isolation techniques require optimization to maximize the yield, viability and quality of the samples, with inherent fluctuations from sample to sample despite maximum optimization. Here, we report a reproducible protocol, involving fixation prior to enzymatic digestion of the heart, which leads to maximum yield while preserving the in vivo morphology of individual cardiomyocytes. We further developed an automated analysis platform to determine the number of nuclei and DNA content per nucleus for individual cardiomyocytes. After exposing the chest cavity, the heart was arrested in diastole by perfusion with 60 mM KCl in PBS. Next, the heart was fixed in 4% paraformaldehyde (PFA) solution, and then digested with 60 mg/mL collagenase solution. After digestions, cells were singularized by trituration, and the cardiomyocyte fraction was enriched via differential centrifugation. Isolated cardiomyocytes were stained for Troponin T and &#945;-actinin to assess purity of the obtained population. Furthermore, we developed an image analysis platform to determine cardiomyocyte nucleation and ploidy status following DAPI staining. Image based ploidy assessments led to consistent and reproducible results. Thus, with this protocol, it is possible to preserve native morphology of individual cardiomyocytes to allow immunocytochemistry and DNA content analysis while achieving maximum yield.

Cardiomyocytes were isolated according to the protocol described above. Using this method, we typically get uniformly singularized cardiomyocytes that are relatively pure without contaminating non-cardiomyocyte cells (Figure 1A). Cardiomyocytes are easily identified under bright field microscopy due to their characteristic size and birefringence. This technique is easy to implement and provides consistent results from different isolations with comparable cardiomyocyte yields and quality (Figure 1B). Isolated cardiomyocytes can be stored at 4 &#176;C for several weeks before further use.
Cardiomyocytes that were isolated according to the above protocol can be used for various downstream applications, such as measuring cardiomyocyte size, cardiomyocyte ploidy and immunocytochemistry. As a representative result, we show that cardiomyocytes isolated according to this protocol can be stained using antibodies and fluorochrome-conjugated azides for click chemistry to detect localization of specific proteins or to detect cardiomyocyte DNA replication, respectively. For example, we stained cardiomyocytes with antibodies recognizing &#945;-actinin to show the characteristic z-line staining pattern of sarcomeres (Figure 2A). In a separate experiment, we administered the thymidine analog 5-Ethynyl-2&#39;-deoxyuridine (EdU) to mice before isolating fixed cardiomyocytes. After cardiomyocyte isolation, we stained for incorporated EdU using standard protocols13, and were able to detect cardiomyocytes that had undergone S phase in either mononucleated, binucleated and trinucleated cardiomyocytes (Figure 2B).
To further expand the utility of the isolation method, we developed a pipeline that allows quantification of cardiomyocyte ploidy based on integrated DNA staining. To be able to measure ploidy status of cells or nuclei, we needed to segment nuclei and cardiomyocytes. Figure 3 shows a representation of the strategy we used to identify individual nuclei. First, the original image DNA stained image (Figure 3A) is thresholded based on intensity (Figure 3B). Here, we used DAPI to stain for DNA, but any other nuclear dye that shows a linear correlation with DNA content would work. The program allows for any of Fiji&#39;s intensity thresholding methods to be chosen, but in this example Otsu&#39;s method was used. Nuclear masks that are touching the edge of the image or are smaller than the specified minimum pixel area threshold are excluded. Then, ellipses are fit to the nuclear masks, segmenting individual nuclei. Figure 3C shows these ellipses overlaid on the original image. Next, holes are filled in the masks, and the pixels of the image are then partitioned into territories based on which ellipse they are most proximal to (Figure 3D). The borders of these territories are then used to draw lines through nuclear clusters, finishing the nuclear segmentation process (Figure 3E).
The next step involves detection of cardiomyocytes. For cardiomyocyte images that are obtained based on fluorescently stained cells (Figure 4A), the process is very similar to that for nuclei. The image is thresholded based on an intensity value calculated by the selected thresholding method, in this case the triangle method. Identified cardiomyocyte masks that are touching the boundary of the image or are below a certain size are excluded and holes are filled in the masks to provide properly segmented cardiomyocytes (Figure 4B). Because cardiomyocytes have a more irregular shape than nuclei, no attempt is made to segment cardiomyocyte clusters. Instead, these clusters are excluded based on their high minimum Feret&#39;s diameter during the analysis step. Segmentation from bright field images proceeds slightly differently. First, the original bright field image (Figure 4C) is processed with a Sobel edge filter. This filter calculates the absolute value of the gradient of each pixel within the image. Pixels in regions with rapid changes receive high values and pixels in smooth regions of the image receive low values. This edge-filtered image is then thresholded by intensity, using the Triangle method, resulting in masked cardiomyocytes (Figure 4D). These highly irregular masks are then smoothed and linked together via morphological closing using a circle with a radius of 2 pixels, which fills in all white regions in the image where the circle cannot fit without overlapping a black region (Figure 4E). Finally, holes in the masks are filled, regions touching the border are excluded, and small particles are removed, finishing the cardiomyocyte segmentation process (Figure 4F).
Using the outlined segmentation strategy, we can then determine the nucleation status of individual cardiomyocytes. Using this approach, we determined the nucleation status of cardiomyocytes isolated from hearts of outbred CD-1 mice at early postnatal time-points. Hearts of newborn mice (first day of life) showed that the majority of cardiomyocytes at that point are mononucleated (Figure 5: neonatal). This high frequency of mononucleated cardiomyocytes is much lower in juvenile mice (2-week old), where mononucleated cardiomyocytes make up about 25% of the total cardiomyocyte population (Figure 5: juvenile). Finally, we can measure the ploidy status of individual nuclei within cardiomyocytes, and determine whether they are diploid or tetraploid. These results show higher frequency of tetraploid nuclei in adolescent mice (Figure 6).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/60938/60938fig1.jpg" /> 
Figure 1: Efficiency of cardiomyocyte isolation after fixation. (A) Representative image of isolated cardiomyocytes stained with DAPI to show nuclei. (DAPI (blue), Brightfield (gray)) (B) Yield of cardiomyocytes isolated from different mice at 3 months of age. Scale bars = 50 &#181;m. <a href="https://www.jove.com/files/ftp_upload/60938/60938fig1large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 2" class="xfigimg" src="/files/ftp_upload/60938/60938fig2.jpg" /> 
Figure 2: Immunocytochemistry of isolated cardiomyocytes. (A) Representative image of cardiomyocytes stained for &#945;-actinin (&#945;-actinin (red) and DAPI (blue)). (B) Cardiomyocytes stained for incorporated EdU (red) and DAPI (blue). Representative cardiomyocytes that are mononucleated (left), binucleated (middle) and trinucleated (right) and EdU positive are shown. Scale bars = 50 &#181;m. <a href="https://www.jove.com/files/ftp_upload/60938/60938fig2large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 3" class="xfigimg" src="/files/ftp_upload/60938/60938fig3.jpg" /> 
Figure 3: Strategy for nuclear segmentation. (A) Original DAPI channel image. (B) Thresholded image (in this example, Otsu&#39;s method was used). (C) Masks that were identified from the thresholded images overlaid on the original DAPI stained image. (D) Voronoi tessellation based on nuclear masks. (E) Final segmented nuclei, with split clusters highlighted. Scale bars = 100 &#181;m. <a href="https://www.jove.com/files/ftp_upload/60938/60938fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 4" class="xfigimg" src="/files/ftp_upload/60938/60938fig4.jpg" /> 
Figure 4: Strategy for cardiomyocyte segmentation. (A) Original fluorescent Troponin I stained cardiomyocyte image. (B) Triangle-thresholded image, after filling holes and excluding small objects and those touching the border. (C) Original bright field cardiomyocyte image (D) Edge-filtered and triangle-thresholded cardiomyocyte image (E) Edge-filtered image after morphological closing with a radius of two pixels (F) Same image after filling holes and excluding small objects and those touching the border. Scale bars = 100 &#181;m. <a href="https://www.jove.com/files/ftp_upload/60938/60938fig4large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 5" class="xfigimg" src="/files/ftp_upload/60938/60938fig5.jpg" /> 
Figure 5: Classification of cardiomyocytes based on number of nuclei. Neonatal hearts (1 day old) contain more mononucleated cardiomyocytes than juvenile hearts (14 days old). <a href="https://www.jove.com/files/ftp_upload/60938/60938fig5large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<img alt="Figure 6" class="xfigimg" src="/files/ftp_upload/60938/60938fig6.jpg" /> 
Figure 6: Distribution of cardiomyocyte DNA content per nucleus. In neonates (left), 13.5% of mononucleated CM nuclei are tetraploid and 11.9% of binucleated CM nuclei are tetraploid. In juveniles (right), 33.9% of mononucleated CM nuclei are tetraploid and 31.2% of binucleated CM nuclei are tetraploid. <a href="https://www.jove.com/files/ftp_upload/60938/60938fig6large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Supplementary File 1: Software Screenshots. <a href="https://www.jove.com/files/ftp_upload/60938/SoftwareScreenshots.pdf" target="_blank">Please click here to view this file (Right click to download).</a>
Supplementary File 2: AnalyzeNucleation.py. <a href="https://www.jove.com/files/ftp_upload/60938/AnalyzeNucleation.zip" target="_blank">Please click here to view this file (Right click to download).</a>
Supplementary File 3: AnalyzeMultinucleatedServer.R. <a href="https://www.jove.com/files/ftp_upload/60938/AnalyzeMultinucleatedServer.zip" target="_blank">Please click here to view this file (Right click to download).</a>

Watch this Scientific Journal Video about Isolation of Cardiomyocytes from Fixed Hearts for Immunocytochemistry and Ploidy Analysis at JoVE.com

Isolation of Cardiomyocytes from Fixed Hearts for Immunocytochemistry and Ploidy Analysis

The goal of this work is to develop a method to reproducibly isolate cardiomyocytes from the adult heart and measure DNA content and nucleation.

The adult mammalian heart is composed of various cell types including cardiomyocytes, endothelial cells and fibroblasts. Since it is difficult to reliably ...

isolation-cardiomyocytes-from-fixed-hearts-for-immunocytochemistry

Research

JoVE Journal

Biology

7.0K Views.  University of Minnesota. The goal of this work is to develop a method to reproducibly isolate cardiomyocytes from the adult heart and measure DNA content and nucleation.

Video: Isolation of Cardiomyocytes from Fixed Hearts for Immunocytochemistry and Ploidy Analysis

Visualization of Cell Cycle Variations and Determination of Nucleation in Postnatal Cardiomyocytes

Cardiomyocytes are prone to variations of the cell cycle, such as endoreduplication (continuing rounds of DNA synthesis without karyokinesis and cytokinesis) and acytokinetic mitosis (karyokinesis but no cytokinesis). Such atypical cell cycle variations result in polyploid and multinucleated cells rather than in cell division. Therefore, to determine cardiac turnover and regeneration, it is of crucial importance to correctly identify cardiomyocyte nuclei, the number of nuclei per cell, and their cell cycle status. This is especially true for the use of nuclear markers for identifying cell cycle activity, such as thymidine analogues Ki-67, PCNA, or pHH3. Here, we present methods for recognizing cardiomyocytes and their nuclearity and for determining their cell cycle activity. We use two published transgenic systems: the Myh6-H2B-mCh transgenic mouse line, for the unequivocal identification of cardiomyocyte nuclei, and the CAG-eGFP-anillin mouse line, for distinguishing cell division from cell cycle variations. Combined together, these two systems ease the study of cardiac regeneration and plasticity.

To distinguish cell division from cell cycle variations in cardiomyocytes, we present protocols using two transgenic mouse lines: Myh6-H2B-mCh transgenic mice, for the unequivocal identification of cardiomyocyte nuclei, and CAG-eGFP-anillin mice, for distinguishing cell division from cell cycle variations.

Cardiomyocytes are prone to variations of the cell cycle, such as endoreduplication (continuing rounds of DNA synthesis without karyokinesis and ...

Developmental Biology

Isolation of Cardiomyocyte Nuclei from Post-mortem Tissue

Identification of cardiomyocyte nuclei has been challenging in tissue sections as most strategies rely only on cytoplasmic marker proteins1. Rare events in cardiac myocytes such as proliferation and apoptosis require an accurate identification of cardiac myocyte nuclei to analyze cellular renewal in homeostasis and in pathological conditions2. Here, we provide a method to isolate cardiomyocyte nuclei from post mortem tissue by density sedimentation and immunolabeling with antibodies against pericentriolar material 1 (PCM-1) and subsequent flow cytometry sorting. This strategy allows a high throughput analysis and isolation with the advantage of working equally well on fresh tissue and frozen archival material. This makes it possible to study material already collected in biobanks. This technique is applicable and tested in a wide range of species and suitable for multiple downstream applications such as carbon-14 dating3, cell-cycle analysis4, visualization of thymidine analogues (e.g. BrdU and IdU)4, transcriptome and epigenetic analysis.

Cardiac nuclei are isolated via density sedimentation and immunolabeled with antibodies against pericentriolar material 1 (PCM-1) to identify and sort cardiomyocyte nuclei by flow cytometry.

Identification of cardiomyocyte nuclei has been challenging in tissue sections as most strategies rely only on cytoplasmic marker proteins1. Rare events ...

Medicine

Isolation and Genetic Manipulation of Adult Cardiac Myocytes for Confocal Imaging

Cardiac myocytes isolated from adult hearts are widely accepted as a model somewhere half way between embryonic and neonatal muscle cells on one side and a working heart on the other. Thus, cardiomyocytes serve as good models for cardiac cellular physiology and pathophysiology, for pharmaceutical investigations as well as for the exploration of transgenic animal models. Here we describe a method of isolating the cells from the heart. Furthermore we show how a genetic manipulation on cardiac myocytes can be performed without breeding a transgenic animal: This is the combination of long term culture (1 week) and adenoviral gene transfer. The latter one is described from the construction of the virus to the transduction of the cells. It can be used for the expression of genetically encoded biosensors (GEBs), fluorescent fusion proteins, but also for protein over expression and down regulation, e.g. using RNAi. Here we provide an example for the expression of a fusion protein staining a subcellular structure (Golgi). Such protein expression can be visualized by confocal imaging of z-stacks for a 3D-reconstruction of subcellular structures. The protocol comprises state-of-the-art in cell culture, molecular biology and biophysics and thus provides an approach for exploring new horizons in cellular cardiology.

Adult cardiac myocytes are primary cells that can be isolated from animal hearts and cultured for several days. Within this culture period adenoviral gene transfer can be used to express genetically encoded biosensors (GEBs) or fluorescent fusion proteins. Both approaches allow cellular investigations by means of confocal microscopy.

Cardiac myocytes isolated from adult hearts are widely accepted as a model somewhere half way between embryonic and neonatal muscle cells on one side and ...

Isolation and Identification of Extravascular Immune Cells of the Heart

The immune system is an essential component of a healthy heart. The myocardium is home to a rich population of different immune cell subsets with functional compartmentalization both during steady state and during different forms of inflammation. Until recently, the study of immune cells in the heart required the use of microscopy or poorly developed digestion protocols, which provided enough sensitivity during severe inflammation but were unable to confidently identify small &#8212; but key &#8212; populations of cells during steady state. Here, we discuss a simple method combining enzymatic (collagenase, hyaluronidase and DNAse) and mechanical digestion of murine hearts preceded by intravascular administration of fluorescently-labelled antibodies to differentiate small but unavoidable intravascular cell contaminants. This method generates a suspension of isolated viable cells that can be analyzed by flow cytometry for identification, phenotyping and quantification, or further purified with fluorescence-activated cell sorting or magnetic bead separation for transcriptional analysis or in vitro studies. We include an example of a step-by-step flow cytometric analysis to differentiate the key macrophage and dendritic cell populations of the heart. For a medium sized experiment (10 hearts) the completion of the procedure requires 2&#8211;3 h.

This protocol presents a simple and efficient method to isolate, identify and quantify immune cells residing in the myocardium of mice during steady state or inflammation. The protocol combines enzymatic and mechanical digestion for the generation of a single cell suspension that can be further analyzed by flow cytometry.

The immune system is an essential component of a healthy heart. The myocardium is home to a rich population of different immune cell subsets with ...

Immunology and Infection

Isolating Primary Melanocyte-like Cells from the Mouse Heart

We identified a novel population of melanocyte-like cells (also known as cardiac melanocytes) in the hearts of mice and humans that contribute to atrial arrhythmia triggers in mice. To investigate the electrical and biological properties of cardiac melanocytes we developed a procedure to isolate them from mouse hearts that we derived from those designed to isolate neonatal murine cardiomyocytes. In order to obtain healthier cardiac melanocytes suitable for more extensive patch clamp or biochemical studies, we developed a refined procedure for isolating and plating cardiac melanocytes based on those originally designed to isolate cutaneous melanocytes. The refined procedure is demonstrated in this review and produces larger numbers of healthy melanocyte-like cells that can be plated as a pure population or with cardiomyocytes.

In this protocol, we identified a novel population of melanocyte-like cells (also known as cardiac melanocytes) in the hearts of mice and humans that contribute to atrial arrhythmia triggers in mice.&#160;

We identified a novel population of melanocyte-like cells (also known as cardiac melanocytes) in the hearts of mice and humans that contribute to atrial ...

Isolation, Culture, and Functional Characterization of Adult Mouse Cardiomyoctyes

The use of primary cardiomyocytes (CMs) in culture has provided a powerful complement to murine models of heart disease in advancing our understanding of heart disease. In particular, the ability to study ion homeostasis, ion channel function, cellular excitability and excitation-contraction coupling and their alterations in diseased conditions and by disease-causing mutations have led to significant insights into cardiac diseases. Furthermore, the lack of an adequate immortalized cell line to mimic adult CMs, and the limitations of neonatal CMs (which lack many of the structural and functional biomechanics characteristic of adult CMs) in culture have hampered our understanding of the complex interplay between signaling pathways, ion channels and contractile properties in the adult heart strengthening the importance of studying adult isolated cardiomyocytes. Here, we present methods for the isolation, culture, manipulation of gene expression by adenoviral-expressed proteins, and subsequent functional analysis of cardiomyocytes from the adult mouse. The use of these techniques will help to develop mechanistic insight into signaling pathways that regulate cellular excitability, Ca2+ dynamics and contractility and provide a much more physiologically relevant characterization of cardiovascular disease.

Here we describe the isolation of adult mouse cardiomyoctyes using a Langendorff perfusion system. The resulting cells are Ca2+-tolerant, electrically quiescent and can be cultured and transfected with adeno- or lentiviruses to manipulate gene expression. Their functionality can also be analyzed using the MMSYS system and patch clamp techniques.

The use of primary cardiomyocytes (CMs) in culture has provided a powerful complement to murine models of heart disease in advancing our understanding of ...

Isolation and Physiological Analysis of Mouse Cardiomyocytes

Cardiomyocytes, the workhorse cell of the heart, contain exquisitely organized cytoskeletal and contractile elements that generate the contractile force used to pump blood. Individual cardiomyocytes were first isolated over 40 years ago in order to better study the physiology and structure of heart muscle. Techniques have rapidly improved to include enzymatic digestion via coronary perfusion. More recently, analyzing the contractility and calcium flux of isolated myocytes has provided a vital tool in the cellular and sub-cellular analysis of heart failure. Echocardiography and EKGs provide information about the heart at an organ level only. Cardiomyocyte cell culture systems exist, but cells lack physiologically essential structures such as organized sarcomeres and t-tubules required for myocyte function within the heart. In the protocol presented here, cardiomyocytes are isolated via Langendorff perfusion. The heart is removed from the mouse, mounted via the aorta to a cannula, perfused with digestion enzymes, and cells are introduced to increasing calcium concentrations. Edge and sarcomere detection software is used to analyze contractility, and a calcium binding fluorescent dye is used to visualize calcium transients of electrically paced cardiomyocytes; increasing understanding of the role cellular changes play in heart dysfunction. Traditionally used to test drug effects on cardiomyocytes, we employ this system to compare myocytes from WT mice and mice with a mutation that causes dilated cardiomyopathy. This protocol is unique in its comparison of live cells from mice with known heart function and known genetics. Many experimental conditions are reliably compared, including genetic or environmental manipulation, infection, drug treatment, and more. Beyond physiologic data, isolated cardiomyocytes are easily fixed and stained for cytoskeletal elements. Isolating cardiomyocytes via perfusion is an extremely versatile method, useful in studying cellular changes that accompany or lead to heart failure in a variety of experimental conditions.

Individual cardiomyocytes from wild type and mutant mice can be isolated from the heart in order to study their contractility and calcium transients. This allows characterization of the contribution of cellular dysfunction to heart dysfunction from any cause.

Cardiomyocytes, the workhorse cell of the heart, contain exquisitely organized cytoskeletal and contractile elements that generate the contractile force ...

Isolation and Purification of Murine Cardiac Pericytes

Pericytes, perivascular cells of microvessels and capillaries, are known to play a part in angiogenesis, vessel stabilization, and endothelial barrier integrity. However, their tissue-specific functions in the heart are not well understood. Moreover, there is currently no protocol utilizing readily accessible materials to isolate and purify pericytes of cardiac origin. Our protocol focuses on using the widely used mammalian model, the mouse, as our source of cells. Using the enzymatic digestion and mechanical dissociation of heart tissue, we obtained a crude cell mixture that was further purified by fluorescence activating cell sorting (FACS) by a plethora of markers. Because there is no single unequivocal marker for pericytes, we gated for cells that were CD31-CD34-CD45-CD140b+NG2+CD146+. Following purification, these primary cells were cultured and passaged multiple times without any changes in morphology and marker expression. With the ability to regularly obtain primary murine cardiac pericytes using our protocol, we hope to further understand the role of pericytes in cardiovascular physiology and their therapeutic potential.

We have optimized a protocol to isolate and purify murine cardiac pericytes for basic research and investigation of their biology and therapeutic potential.

Pericytes, perivascular cells of microvessels and capillaries, are known to play a part in angiogenesis, vessel stabilization, and endothelial barrier ...

A Simple and Effective Method to Consistently Isolate Mouse Cardiomyocytes

The need for reproducible yet technically simple methods yielding high-quality cardiomyocytes is essential for research in cardiac biology. Cellular and molecular functional experiments (e.g., contraction, electrophysiology, calcium cycling, etc.) on cardiomyocytes are the gold standard for establishing mechanism(s) of disease. The mouse is the species of choice for functional experiments and the described technique is specifically for the isolation of mouse cardiomyocytes. Previous methods requiring a Langendorff apparatus require high levels of training and precision for aortic cannulation, often resulting in ischemia. The field is shifting toward Langendorff-free isolation methods that are simple, are reproducible, and yield viable myocytes for physiological data acquisition and culture. These methods greatly diminish ischemia time compared to aortic cannulation and result in reliably obtained cardiomyocytes. Our adaptation to the Langendorff-free method includes an initial perfusion with ice-cold clearing solution, use of a stabilizing platform that ensures a steady needle during perfusion, and additional digestion steps to ensure reliably obtained cardiomyocytes for use in functional measurements and culture. This method is simple and quick to perform and requires little technical skill.

The gold standard in cardiology for cellular and molecular functional experiments are cardiomyocytes. This article describes adaptations to the non-Langendorff technique to isolate mouse cardiomyocytes.

The need for reproducible yet technically simple methods yielding high-quality cardiomyocytes is essential for research in cardiac biology. Cellular and ...

Isolation of Human Ventricular Cardiomyocytes from Vibratome-Cut Myocardial Slices

The isolation of ventricular cardiac myocytes from animal and human hearts is a fundamental method in cardiac research. Animal cardiomyocytes are commonly isolated by coronary perfusion with digestive enzymes. However, isolating human cardiomyocytes is challenging because human myocardial specimens usually do not allow for coronary perfusion, and alternative isolation protocols result in poor yields of viable cells. In addition, human myocardial specimens are rare and only regularly available at institutions with on-site cardiac surgery. This hampers the translation of findings from animal to human cardiomyocytes. Described here is a reliable protocol that enables efficient isolation of ventricular myocytes from human and animal myocardium. To increase the surface-to-volume ratio while minimizing cell damage, myocardial tissue slices 300 &#181;m thick are generated from myocardial specimens with a vibratome. Tissue slices are then digested with protease and collagenase. Rat myocardium was used to establish the protocol and quantify yields of viable, calcium-tolerant myocytes by flow-cytometric cell counting. Comparison with the commonly used tissue-chunk method showed significantly higher yields of rod-shaped cardiomyocytes (41.5 &#177; 11.9 vs. 7.89 &#177; 3.6%, p &#60; 0.05). The protocol was translated to failing and non-failing human myocardium, where yields were similar as in rat myocardium and, again, markedly higher than with the tissue-chunk method (45.0 &#177; 15.0 vs. 6.87 &#177; 5.23 cells/mg, p &#60; 0.05). Notably, with the protocol presented it is possible to isolate reasonable numbers of viable human cardiomyocytes (9&#8211;200 cells/mg) from minimal amounts of tissue (&#60;50 mg). Thus, the method is applicable to healthy and failing myocardium from both human and animal hearts. Furthermore, it is possible to isolate excitable and contractile myocytes from human tissue specimens stored for up to 36 h in cold cardioplegic solution, rendering the method particularly useful for laboratories at institutions without on-site cardiac surgery.

Presented is a protocol for the isolation of human and animal ventricular cardiomyocytes from vibratome-cut myocardial slices. High yields of calcium-tolerant cells (up to 200 cells/mg) can be obtained from small amounts of tissue (&#60;50 mg). The protocol is applicable to myocardium exposed to cold ischemia for up to 36 h.

The isolation of ventricular cardiac myocytes from animal and human hearts is a fundamental method in cardiac research. Animal cardiomyocytes are commonly ...