The authors thank T. Yamamoto and Y. Mori for their assistance in the morphologic experiments. This work was supported by a Grant-in-Aid for Scientific Research (C) from the Japan Society for the Promotion of Science (18K06871 to M.O.K. and 17K08536 to H.M.).

All animal experiments conformed to the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH Publication No. 85-23, revised 1996) and were approved by the institutional Review Board of the Shiga University of Medical Science Animal Care and Use Committee (approved No. 2019-3-7). The methods were carried out in accordance with approved guidelines.
1. Instruments and solution
NOTE: An outline of the experimental procedure is illustrated in a flow diagram (Supplementary Figure 1). An infusion pump (or syringe pump) should be used for the antegrade perfusion of the heart with a one-way flow. A peristaltic pump that creates a pulsating flow is not recommended.
<ol>
	<li>Before the experimental
	<ol>
		<li>Mark the injection needle at a site approximately 3 mm from the tip with nail polish. After allowing it the air dry, keep it in the container at room temperature. A red or bright color is desirable to confirm the depth of insertion into the myocardium during perfusion.</li>
		<li>Make the heart stand by cutting the lids off of 1.5-, 0.5- and 0.2-mL sample tubes and attaching the lids to the bottom of a 60-mm culture dish with double-sided tape or adhesive. Fixation of three different-sized lids in one dish makes it possible to choose the appropriate one according to the size of the mouse heart. This heart stand can be reused after washing.</li>
		<li>Make stock solution as shown in Table 1. Store the stock solutions at 4 &#176;C.</li>
	</ol>
	</li>
	<li>On the experiment day 
	NOTE: Cell isolation buffer (CIB) contains (in mM) 130 NaCl, 5.4 KCl, 0.5 MgCl2, 0.33 NaH2PO4, 22 glucose, 40 units/mL insulin and 25 HEPES (pH adjusted to 7.4 with NaOH); and Tyrode solution contains (in mM) 140 NaCl, 5.4 KCl, 1.8 CaCl2, 0.5 MgCl2, 0.33 NaH2PO4, 5.5 glucose and 5.0 HEPES (pH adjusted to 7.4 with NaOH).
	<ol>
		<li>Prepare the CIB. Warm 160 mL of distilled water (DW) using a microwave to around 32 &#176;C and then add 20 mL of 10X CIB. After the addition of 0.79 g glucose and 10 &#181;L of insulin solution, adjust the pH using 1 M NaOH and bring to 200 mL with DW.</li>
		<li>Prepare the enzyme mix solution (enzyme mix). Add 30 mg of collagenase, 1.8 mg of trypsin, 1.8 mg of protease and 90 &#181;L of 100 mM CaCl2 stock solution to 30 mL of CIB (final Ca2+ concentration is 0.3 mM), mix, and keep it on ice. In mice &#60;4 weeks old, reduce trypsin and protease to 0.9 mg10. Warm at 37 &#176;C in a water bath before use.</li>
		<li>Prepare the CIB-Ca2+-BSA solution. Add 30 mg BSA and 90 &#181;L of 100 mM CaCl2 stock solution to 15 mL of CIB (final Ca2+ concentration is 1.2 mM), mix, filter through a 20-&#181;m filter, and keep it on ice.</li>
		<li>Prepare the CIB-EGTA solution. After making the solutions described in steps 1.2.2 and 1.2.3, add 400 mM EGTA stock solution to the remaining CIB at a 1:1000 dilution (final EGTA concentration is 0.4 mM), and mix. Fill the 35-mm culture dish and heart stand dish with CIB-EGTA and keep them on ice.
		<ol>
			<li>Pour approximately 20 mL of CIB-EGTA into a 30-mL glass beaker and stand a plastic transfer pipette in the beaker, keeping it on ice.</li>
		</ol>
		</li>
		<li>Prepare Tyrode solution. Add 100 mL of 10X&#160;Tyrode to 800 mL of DW and warm it using a microwave to around 32 &#176;C. After adding 0.99 g of glucose and 1.8 mL of 1 M CaCl2, adjust the pH using 1 M NaOH and bring to 1000 mL with DW.</li>
		<li>Prepare the cell resuspension solution. Add 30 mg of BSA and 300 &#181;L of 50X&#160;antibiotics to 15 mL of Tyrode solution.</li>
		<li>Prepare syringes. Fill the 20-mL syringe connected with the flexible extension tube and the marked injection needle with CIB-EGTA. Fill the 30-mL syringe with the warmed enzyme mix. Hold them both at 37 &#176;C until just before use.</li>
		<li>Prepare the perfusion plate. Prewarm the heater mat under a stereoscopic microscope. Place the perfusion plate (lid of a multi-well culture plate) on the prewarmed heater mat. Prewarm the vascular clamp by placing it in the perfusion plate until use. Place the 60-mm culture dish for pipetting and the cell strainer on the prewarmed heater mat as well.</li>
	</ol>
	</li>
</ol>
2. Antegrade perfusion of the mouse heart
NOTE: The plastic transfer pipette used for sucking the heart should be soft and not be sharply tapered towards the tip. Choose a small vascular clamp with serration. The recommended instruments are listed in the Table of Materials.
<ol>
	<li>Excision of the mouse heart and clamping the aorta 
	NOTE: The adult mice (&#62;8 weeks old) should be euthanized by an overdose of sodium pentobarbital (&#62;300 mg/kg, intraperitoneal [i.p.] injection) with heparin (8000 unit/kg).
	<ol>
		<li>Excise the mouse heart quickly by sucking.
		<ol>
			<li>Open the thoracic cavity quickly to expose the heart. Cut the plastic transfer pipette, the tip of which is approximately the same size as, or slightly smaller than, the exposed heart (usually at a site approximately 1 cm from the 0.5-mL mark towards the tip, but it depends on the heart size).</li>
			<li>Suck the heart into the pipette, raise the pipette to create enough space to insert scissors, and excise the heart with curved scissors from the dorsal side, avoiding damaging the atria.</li>
			<li>Immediately transfer the excised heart to the 30-mL glass beaker containing ice-chilled CIB-EGTA to stop the contraction. This procedure usually takes &#60;1 min.</li>
		</ol>
		</li>
		<li>Cleaning around the aorta
		<ol>
			<li>Transfer the heart to a 35-mm culture dish filled with ice-chilled CIB-EGTA and remove the lung and other visible tissues, and then transfer the roughly cleaned heart to the heart stand filled with chilled CIB-EGTA and place it with the apex down.</li>
			<li>Under the stereoscopic microscope, remove the fat and connective tissues to clean around the aorta. If the length of the cut aorta is too long including the brachiocephalic artery, the left common carotid artery or the left subclavian artery, cut off the aorta just under the brachiocephalic artery to shorten it in order to proceed to the next step. This procedure usually takes approximately 4 min.</li>
		</ol>
		</li>
		<li>Clamping the aorta and placing the clamped heart on the perfusion plate
		<ol>
			<li>Under the microscope, place the heart in the heart stand. The operator should face the anterior surface of the heart, pick up the end of the aorta with tweezers, and clamp the aorta near the atria with a small vascular clamp while gently pushing down on the aorta a bit.</li>
			<li>Place the clamped heart on the perfusion plate with the anterior side up, and then cover it with a few drops of CIB-EGTA to keep it from drying out. This procedure usually takes &#60;20 s.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Antegrade perfusion of the heart 
	NOTE: First, perfuse the heart with CIB-EGTA to discharge blood and prevent clotting.
	<ol>
		<li>Insert the injection needle and start perfusion to discharge blood
		<ol>
			<li>Set the 20-mL syringe filled with prewarmed CIB-EGTA connected to the flexible extension tube and a marked injection needle on the infusion pump. Start the pump at a slow rate of 0.5 mL/min to carefully fill the needle and tube with CIB-EGTA and be sure to prevent any air from entering the tube.</li>
			<li>Place the injection needle on the perfusion plate with the shorter side of the diagonal shape in front. Slide the needle towards the apex of the heart until it is touching it, and then carefully insert the needle near the apex of the left ventricle into the ventricular chamber without twisting. Do not detach the needle from the plate while performing insertion.</li>
			<li>Watch the red mark to estimate the depth of the needle insertion. When the needle insertion is completed, blood flowing from the coronary artery should start to be discharged.</li>
			<li>Fix the injection needle on the plate with tape, and increase the pump speed to 1 mL/min. This procedure usually takes approximately 30 s. If the heart is perfused successfully, the flow of the CIB-EGTA in the capillary just under the epicardium can be seen under the microscope.</li>
		</ol>
		</li>
		<li>Perfusion the heart with enzyme mix 
		NOTE: During enzymatic perfusion, the depth of the inserted needle can be monitored by checking the red mark on the needle.
		<ol>
			<li>After perfusing 2-3 mL of CIB-EGTA to completely discharge blood from the coronary artery, change the perfusate to enzyme mix. Avoid allowing air bubbles to enter the tube. Check the flow of the enzyme mix, and ensure that the injection needle has not come out by checking the position of the red mark.</li>
			<li>After 1-2 mL has been perfused, increase the pump speed to 1.5 mL/min. Remove the accumulated perfusate containing blood that has flowed out of the heart with a pipette from time to time. 
			NOTE: Over time, the myocardial wall will become translucent in some places and appear mottled, which is a sign of digestion of the extracellular matrix following successful perfusion. Another sign is the restarting of atrial beating caused by the presence of Ca2+ in the enzyme mix.</li>
			<li>Stop perfusion when the total volume of the enzyme mix perfused is 10 mL.</li>
		</ol>
		</li>
	</ol>
	</li>
</ol>
3. Isolation of individual heart cells
<ol>
	<li>Dissociating heart cells
	<ol>
		<li>After perfusion with the enzyme mix, transfer 10 mL of the enzyme mix remaining in the syringe to a 60-mm culture dish placed on the heater mat and add 20 mg of BSA (0.2% BSA in enzyme mix). The dropped BSA powder should dissolve immediately by gently swirling with a hand. Remove the injection needle and the vascular clamp from the heart.</li>
		<li>Separate the ventricles and atria and transfer each into the enzyme mix supplemented with 0.2% BSA on the heater mat.</li>
	</ol>
	</li>
	<li>Isolation of ventricular myocytes
	<ol>
		<li>Grab the epicardium with two tweezers, and gently tear and pull the ventricles from side to side in the enzyme mix supplemented with 0.2% BSA into small pieces. Disperse the cells with gentle pipetting (approximately 30 times).</li>
		<li>Filter the undigested debris through a 100-&#181;m mesh cell strainer, and transfer the filtrate to a 15-mL centrifuge tube for centrifugation at 50 &#215; g for 3 min. Resuspend the pelleted cardiomyocytes in prewarmed CIB-Ca2+-BSA solution, incubate it for 5 min at 37 &#176;C, and then centrifuge it at 14 &#215; g for 3 min.</li>
		<li>Resuspend the final precipitated cardiomyocytes in cell resuspension solution (composition is listed in Table 2) and hold it at 37 &#176;C.</li>
	</ol>
	</li>
	<li>Isolation of atrial myocytes
	<ol>
		<li>During the final centrifugation for the ventricular myocyte fraction in step 3.2, start isolating the atrial myocytes. Transfer the atria, stored as in step 3.1, to the prewarmed CIB-Ca2+-BSA solution, tear it into pieces and dissociate the cells by pipetting with pipette tip at 10 &#181;L on the heater mat.</li>
		<li>Centrifuge the cell mixture at 14 &#215; g for 3 min and resuspend the pelleted atrial cells with cell resuspension solution.</li>
	</ol>
	</li>
	<li>Isolation and culture of cardiac fibroblasts
	<ol>
		<li>Transfer the supernatant from the first centrifugation in step 3.2 to another 15-mL centrifuge tube, and centrifuge at 190 &#215; g for 5 min. Wash the precipitated cells twice with centrifugation in Dulbecco&#39;s Modified Eagle Medium (DMEM), and then suspend the cells with DMEM supplemented with 10% fetal bovine albumin (FBS) and antibiotics.</li>
		<li>Plate the final cell fraction in a culture flask (25 cm2) and allow the cells to adhere to the bottom of the flask in a humidified atmosphere of 95% air and 5% CO2. After 90 min incubation, discard the unattached cells, and add fresh culture medium. Cells should near confluency after approximately 4 days, at which point they should be amplified by trypsinization and seeded into new culture dishes.</li>
	</ol>
	</li>
</ol>
4. Harvesting proteins from atria and ventricles
<ol>
	<li>After perfusion, separate the atria and ventricles, and homogenize them in lysis buffer at a ratio of 10 mg of tissue weight to 100 &#181;L of buffer using a small grinder in a 1.5-mL sample tube.</li>
	<li>Keep the homogenate in ice for 40 min with vortex mixing every 10 min to extract proteins, and then centrifuge the tube at 15000 &#215; g for 20 min at 4 &#176;C. Store the supernatant fraction at -80 &#176;C as a protein sample.</li>
</ol>
5. Immunostaining of isolated heart cells
NOTE: Immobilization of non-adherent cardiomyocytes to the bottom of the cell imaging dish using biological glue is necessary.
<ol>
	<li>Adhesion of isolated cardiomyocytes to a glass-bottom culture dish
	<ol>
		<li>Before starting cell isolation, coat the glass-bottom culture dish with biological glue (e.g., Cell-Tak) according to the manufacturer&#39;s instruction, rinse with DW, and air-dry at room temperature.</li>
		<li>After resuspension of the isolated cardiomyocytes in CIB-Ca2+-BSA solution, drop the cell suspension on the bottom of the glue-coated dishes, and incubate for 20 min at room temperature without agitation.</li>
	</ol>
	</li>
	<li>Immunostaining
	<ol>
		<li>Plate the isolated cardiomyocytes on a glass-bottom dish precoated with biological glue and keep it at room temperature for 40 min to allow the cells to adhere to the dish. Culture cardiac fibroblasts in bottom-glass culture dishes.</li>
		<li>Rinse cells with phosphate-buffered saline (PBS), and fix them with 4% paraformaldehyde (PFA) for 5 min with shaking. Wash the fixed cells with PBS for 10 min three times, and incubate them in blocking-permeabilization solution for 60 min at room temperature with shaking.</li>
		<li>Probe cells with primary antibody diluted in blocking-permeabilization solution for 60 min at room temperature or overnight at 4 &#176;C. Wash the cells with PBS for 10 min three times, and incubate then with fluorescence-labeled secondary antibody for 60 min at room temperature.</li>
		<li>After washing them three times with PBS for 10 min, stain the nuclei with DAPI (1:10000 dilution in PBS). Analyze the fluorescent signals using a confocal laser scanning microscope.</li>
	</ol>
	</li>
</ol>
6. Whole-cell patch clamp recordings
<ol>
	<li>Fabricate the patch electrodes from a glass capillaries using a horizontal microelectrode puller. The resistance of the electrode ranged from 2 to 4 M&#937; when filled with a K+-rich pipette solution (Table 2). Transfer an aliquot of isolated cardiomyocytes to a recording chamber mounted on the stage of an inverted microscope superfused with Tyrode at a rate of 1 mL/min&#160;at 36-37 &#176;C.</li>
	<li>Record action potentials using the perforated patch-clamp method with K+-rich pipette solution containing 30 mg/mL amphotericin B by applying current pulses of 5-10 ms in duration at a rate of 1 Hz via the patch electrode.</li>
</ol>
7. Western blot analyses
<ol>
	<li>In this study, perform a Western blot analysis of small-molecular-weight proteins, such as atrial marker atrial natriuretic peptide (ANP).</li>
	<li>Dissolve the protein sample in the final concentration of 1X Sample buffer, 2% 2&#39; mercaptoethanol, and denature the proteins for 60 min at 37 &#176;C. Load 20 &#181;g of protein into each well, and perform electrophoresis in running buffer with 20 mA per gel for 120 min.</li>
	<li>Transfer the protein to a PVDF membrane in transfer buffer at 10 V for 40 min. Wash the transferred membrane twice with TBST for 5 min, then block with 5 % skim milk in TBST for 60 min at room temperature, and probe with the primary antibody dissolved in TBST overnight at 4 &#176;C.</li>
	<li>Wash the membrane 5 times with TBST for 7 min, and incubate it with the secondary antibody diluted in TBST for 120 min at room temperature.</li>
	<li>After washing the membrane 5 times with TBST for 7 min, visualize the signals with a chemi-luminescence assay and analyze them with a lumino-image analyzer.</li>
</ol>

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The authors have nothing to disclose.

Since the heart is highly susceptible to ischemia, the time taken to excise the heart and immerse it in ice-cold CIB-EGTA to stop contraction should be kept short as possible (&#60;1 min). This is the first critical step of this method. The second critical step concerns the direction of the heart. The particular orientation of the excised heart in step 2.1.2 makes it easier to see and remove the fat and connective tissues around the aorta. After cleaning around the aorta, place the clamped heart with anterior surface side up on the perfusion plate. The final critical step involves the insertion of the injection needle. When advancing the needle towards the heart, the injection needle should not be detached from the perfusion plate in order to maintain a constant distance from the plate. The position of the insertion is near the apex of the left ventricle. Insert the needle carefully without twisting, since such twisting may enlarge the hole. The depth of the insertion of the needle can be estimated by watching the red mark. If the needle is inserted too deep, the tip may pierce through the ventricular septum and enter the right ventricle or though the mitral valve and enter the left atrium. After confirming the disappearance of the blood from the coronary artery, the needle should be fixed with tape to the perfusion plate.
A longer aorta length makes it difficult to clamp the aorta at the right position. If the clamp is too distant from the atria, the heart may rotate after perfusate infusion. To prevent this, cut off the aorta just under the brachiocephalic artery to shorten the aorta before clamping.
If the blood does not begin to discharge after perfusion at an initial speed of 0.5 mL/min, increase the speed to 1 mL/min. If that does not help, the injection needle may be positioned incorrectly, such as in the right ventricle, ventricular septum or left myocardial wall. In such a case, remove the needle immediately and try to re-insert it near the apex of the left ventricle. When inserting the needle several times, digested cells may flow out from the opened holes. Note that this does not usually seriously affect the cell isolation.
The operators can monitor the entire process of antegrade perfusion of the heart using a stereoscopic microscope to observe the changes in color and transparency and restarting of the beating of the atria along with the digestion. A total of 10 mL of enzyme mix should be the maximum required, even for an old heart. In younger hearts (5-7 weeks old), we reduce the volume to 9 mL, which is similar to the approach via retrograde perfusion with the same enzyme mix.
The supernatant at the final centrifugation contains debris, blood cells, and non-myocytes whereas, the pellet contains mainly cardiomyocytes and contaminating non-myocytes, such as fibroblasts and endothelial cells. To purify the cardiomyocytes, more steps are needed. In general, the pellet should be resuspended in the appropriate cell culture medium and preplated for 2 h at 37&#176;C on a tissue cell culture dish, and then gently remove the cardiomyocytes by pipetting and preplating for culture.
The enzyme mix contains a low concentration of Ca2+ (0.3 mM). We therefore incubate digested cells in CIB-Ca2+-BSA (1.2 mM Ca2+) before the final resuspension with the cell resuspension solution (1.8 mM Ca2+), and the gradual increase in Ca2+ avoids causing cell damage7. As long as the isolated cardiomyocytes are intact (quiescent cells with no contraction) this Ca2+-adapting procedure does not affect cell viability in mice. As the damaged cells are dying during this incubation, we consequently obtain a healthy cell group. Similarly, isolated intact atrial myocytes (quiescent cells without irregular contraction) can be stored in the same cell resuspension solution. However, the atrial myocytes tend to be more delicate to be stored compare to the ventricular myocytes.
In the laboratory, this isolation method is almost always successful unless the needle insertion into the left ventricle fails. We have also succeeded in isolating cells from the hypertrophied heart prepared by surgical transverse aortic constriction. However, in aged mice, which often have small myocardial infarctions, perfusion ceases in some places, resulting in incomplete digestion and thus a low yield (Figure 1C), similar to the Langendorff-based retrograde method. In such cases, the distorted shape of the heart can be observed even at the start of perfusion.
This antegrade perfusion method is useful for isolating heart cells from mice of various ages but not larger animals, such as rabbits and guinea pigs. It may be possible to apply this method to neonatal or juvenile rats before weaning.
One of the advantages of this antegrade perfusion method is that it decreases the technical obstacles associated with using the Langendorff-based retrograde perfusion method for small mouse hearts. The time required for perfusion is approximately 7 min with 10 mL of the enzymes, this short digestion period increases the viability of the cells. In addition, it enables perfusion to be performed through the coronary circulation of the heart, even after the aortic valves have been digested. Isolation of atrial myocytes usually requires Langendorff-based retrograde perfusion and further incubation with enzymes17. This antegrade perfusion approach, however, can deeply perfuse the tissue with the enzyme to isolate atrial myocytes.
In experiments using multiple mice, the Langendorff apparatus should be cleaned before perfusing the next heart. However, in the present antegrade method, as long as desired number of instrument sets (e.g., syringes needles and perfusion plates) are prepared in advance, perfusion can be performed continuously.
We herein report the basic methodology of the antegrade perfusion of the mouse heart using the same solutions as the Langendorff-based retrograde perfusion method with no additional chemicals. The composition of the perfusate can be changed to suit the purpose of the experiment, such as using a detergent containing EGTA instead of the enzymes to make a decellularized heart18.

Generally, the first step of the single cell isolation of dissected tissue involves mincing the tissue into small pieces, followed by the digestion of the connective tissue and extracellular matrix with enzymes. However, cardiomyocytes cannot be isolated with such a chopping method, as enrichment with extracellular matrix components, including collagen and elastin fibers, makes the myocardium too tough to mince, and the cardiomyocytes are highly sensitive to hypoxia and other changes in the microenvironment. Thus, using the Langendorff-based retrograde perfusion system1, a method of digesting the extracellular matrix with enzymes has been developed to isolate individual cardiomyocytes from the heart2,3,4.
In mouse models, Langendorff-based retrograde perfusion of the heart with enzymes is also used for the isolation of individual cardiomyocytes5,6,7,8.&#160;However, the cannulation of the small and thin mouse aorta and its mounting on the Langendorff apparatus to perform retrograde perfusion requires a high degree of skill, since the diameter of the aorta in the adult heart is approximately 1.2 mm. Furthermore, it takes time to perform multiple experiments as the Langendorff apparatus should be cleaned before perfusing the next heart.
As an alternative to retrograde perfusion, a novel method for isolating cardiomyocytes from an adult mouse heart without a Langendorff apparatus was developed. This epoch-making method was based on the antegrade perfusion of the coronary arteries9. We recently improved each step of this antegrade protocol, such as the clamping of the aorta, needle insertion, and temperature control, and monitored all perfusion procedures with a microscope10. We herein report in detail the refinement of this antegrade perfusion method to shorten the time for isolation and provide a supplemental video. In this method, the perfusion of the heart takes approximately 7 min with 10 mL of the enzymes, and this short digestion period increases the viability of the cells. This is a simple method for isolating single heart cells at a high quality without requiring the addition of chemicals, such as 2,3-butanedione monoxime (BDM)6,11 or taurine5,8. We believe that this method will lower the skill threshold of the technique and enhance the utility of mouse cardiomyocytes in basic research.

<table><tbody><tr><td>Amphotericin B</td><td>Wako Pure Chemical Industries, Japan</td><td></td><td></td></tr><tr><td>Alexa Fluor 488 anti-mouse IgG antibody</td><td>Molecular Probes, USA</td><td>A11001</td><td>Fluorescent-labeled secondary antibody. (1:400 dilution for immunostaining)</td></tr><tr><td>Anti-&amp;alpha;-actinin (ACTN)</td><td>Sigma-Aldrich, USA</td><td>A7811</td><td>Mouse monoclonal antibody (clone EA-53). (1:400 dilution for immunostaining)</td></tr><tr><td>Anti-atrial natriuretic peptide (ANP)</td><td>Merck-Millipore, USA</td><td>AB5490-I</td><td>Rabbit polyclonal antibody (1:2000 dilution for Western blots)</td></tr><tr><td>Anti-Glyceraldehyde 3-phosphate dehydrogenase (GAPDH)</td><td>Cell Signaling Technology, USA</td><td>2118</td><td>Mouse monoclonal antibody (1:10000 dilution for Western blots)</td></tr><tr><td>Anti-smooth muscle actin (SMA)</td><td>Dako, Denmark</td><td>M0851</td><td>Mouse monoclonal antibody (clone 1A4) (1:400 for immunostaining)</td></tr><tr><td>Anti-rabbit IgG antibody</td><td>Amersham, GE Healthcare, USA</td><td>NA934</td><td>Secondary antibody (1:10000 dilution for Western blots)</td></tr><tr><td>ATP disodium salt</td><td>Sigma-Aldrich, USA</td><td>A26209</td><td></td></tr><tr><td>Bovine serum albumin (BSA)</td><td>Sigma-Aldrich, USA</td><td>A9418</td><td></td></tr><tr><td>Cell-Tak</td><td>Corning</td><td>354240</td><td>Biological material for adhesion of the cell or tissues</td></tr><tr><td>Chemi-Lumi One Super&amp;nbsp;</td><td>Nacalai Tesque, Japan</td><td>02230-14</td><td>Chemiluminescent reagent used for western blotting.</td></tr><tr><td>Collagenase Type 2</td><td>Worthington Biochemicals, USA</td><td>LS004176</td><td>Choose the activity guaranteed to be greater than 300 unit/mg.</td></tr><tr><td>Complete Mini</td><td>Roche, Germany</td><td>11836153001</td><td>A mixture of several protease inhibitors.</td></tr><tr><td>4&#039;6&#039;diamidino-2-phenylindole (DAPI)</td><td>Nacalai Tesque, Japan</td><td>11034-56</td><td>Used for cell-impermeant nuclear stainig&amp;nbsp;</td></tr><tr><td>Dulbecco&#039;s Modified Eagle&#039;s Medium (DMEM)</td><td>Nacalai Tesque, Japan</td><td>08458-45</td><td>including 4.5 g/L gluose</td></tr><tr><td>Extension tube</td><td>Top, Japan</td><td>X1-50</td><td>Connect with syringe and injection needle for antegrade perfusion.&amp;nbsp;</td></tr><tr><td>EPC-8 patch-clamp amplifier</td><td>HEKA, Germany</td><td></td><td></td></tr><tr><td>Fetal bovine serum (FBS)</td><td>Sigma-Aldrich, USA</td><td>F7524-500ML</td><td></td></tr><tr><td>Glass capillaries</td><td>Narishige Scientific Instrument Lab., Japan</td><td></td><td>outside diameter 1.5 mm, inside diameter 0.9 mm</td></tr><tr><td>GTP lithium salt</td><td>Sigma-Aldrich, USA</td><td>G5884</td><td></td></tr><tr><td>Horizontal microelectrode puller&amp;nbsp;</td><td>Germany)</td><td>P-97</td><td></td></tr><tr><td>Heater mat</td><td>Natsume Seisakusho, Japan</td><td>KN-475-3-40</td><td>Equipment to warm the perfusion plate.</td></tr><tr><td>Infusion pump</td><td>TERUMO, Japan</td><td>TE-311</td><td>Infusion syringe pump for antegrade perfusion.</td></tr><tr><td>Injeciton needle (27 gauge)</td><td>TERUMO, Japan</td><td>NN-2719S</td><td>Needle for insertion into the left ventricle.</td></tr><tr><td>Insulin (from bovine pancrease)</td><td>Sigma-Aldrich, USA</td><td>I5500</td><td>Dissolve in 0.1 M HCl.</td></tr><tr><td>Mini cordless grinder</td><td>Funakoshi, Japan</td><td>cG-4A</td><td>Small grinder for homogenizing tissue in 1.5 mL sample tube.</td></tr><tr><td>4%-Paraformaldehyde Phosphate Buffer solution (4% PFA)</td><td>Nacalai Tesque, Japan</td><td>09154-85</td><td></td></tr><tr><td>Penicillin G potassium</td><td>Nacalai Tesque, Japan</td><td>26239-84</td><td></td></tr><tr><td>Phenol Red</td><td>Nacalai Tesque, Japan</td><td>26807-21</td><td></td></tr><tr><td>10X Phosphate Buffered Saline (pH7.4) (10X PBS)</td><td>Nacalai Tesque, Japan</td><td>27575-31</td><td></td></tr><tr><td>Plastic multi-well culture plate</td><td>Falcon, USA</td><td>353226</td><td>Use the lid of the multi-well culture plate as the perfusion plate.</td></tr><tr><td>Plastic syringe (20 mL)</td><td>TERUMO, Japan</td><td>SS-20ES</td><td>Use for infusion of CIB-EGTA.</td></tr><tr><td>Plastic syringe (30 mL)</td><td>TERUMO, Japan</td><td>SS-30ES</td><td>Use for infusion of Enzyme-mix</td></tr><tr><td>Plastic transfer pipette</td><td>Sarstedt, Germany</td><td>86.1171</td><td>Cut the tip just before sucking mouse heart into the pipette.</td></tr><tr><td>Polyvinylidene difluoride (PVDF) membrane</td><td>Merck-Millipore, USA</td><td>IPVH00010</td><td>Immobilin-P membrane (Transfer membrane for protein blotting)</td></tr><tr><td>Protease</td><td>Sigma-Aldrich, USA</td><td>P5147</td><td>A mixture of three or more proteases including extracellular serine protease.</td></tr><tr><td>4X Sample buffer solution</td><td>Fuji Film, Japan</td><td>198-13282</td><td>Contains 0.25 M Tris-HCl (pH 6.8), 8 w/v% SDS,40 w/v% Glyceroland 0.02 w/v% BPB</td></tr><tr><td>SDS polyacrylamide gel&amp;nbsp; (15%)</td><td>Fuji Film, Japan</td><td>193-14991</td><td></td></tr><tr><td>Streptomycin sulfate</td><td>Nacalai Tesque, Japan</td><td>32237-14</td><td></td></tr><tr><td>10X Tris-Glycine buffer solution (10X TG)</td><td>Nacalai Tesque, Japan</td><td>09422-81</td><td>Contains 0.25 M-Tris and 1.92 M-Glycine, (pH 8.3)&amp;nbsp;</td></tr><tr><td>Trypsin</td><td>Sigma-Aldrich, USA</td><td>T8003</td><td>Trypsin from bovine Type 1.&amp;nbsp;</td></tr><tr><td>Vascular clamp</td><td>Karl Hammacher GmbH, Germany</td><td>HSE 004-35</td><td>Small straight vascular clamp used for clamping aorta.</td></tr><tr><td>All other reagents</td><td>Nacalai Tesque, Japan</td><td></td><td></td></tr></tbody></table>

an antegrade perfusion method for cardiomyocyte isolation from mice

In basic research using mouse heart, isolating viable individual cardiomyocytes is a crucial technical step to overcome. Traditionally, isolating cardiomyocytes from rabbits, guinea pigs or rats has been performed via retrograde perfusion of the heart with enzymes using a Langendorff apparatus. However, a high degree of skill is required when this method is used with a small mouse heart. An antegrade perfusion method that does not use a Langendorff apparatus was recently reported for the isolation of mouse cardiomyocytes. We herein report a complete protocol for the improved antegrade perfusion of the excised heart to isolate individual heart cells from adult mice (8 - 108 weeks old). Antegrade perfusion is performed by injecting perfusate near the apex of the left ventricle of the excised heart, the aorta of which was clamped, using an infusion pump. All procedures are carried out on a pre-warmed heater mat under a microscope, which allows for the injection and perfusion processes to be monitored. The results suggest that ventricular and atrial myocytes, and fibroblasts can be well isolated from a single adult mouse simultaneously.

The principle of this method is simple: the perfusate flows from the left chamber, the aortic valve is opened, and the perfusate runs into the coronary artery in the same direction as the blood run, since the aorta is closed by clamping, which enables the deep perfusion of the myocardium in order to digest the extracellular matrix.
Ventricular myocytes freshly isolated with the present method are shown in Figure 1A. Figure 1B shows enlarged images of the ventricular and atrial myocytes. This isolation procedure resulted in a high yield (70%-80%) of rod-shaped quiescent ventricular myocytes from adult mice (8-10 weeks), which were available within roughly 5 h after isolation (Figure 1C), a similar interval to that when using the traditional Langendorff-based procedure7. However, the ratio of freshly isolated viable cells was lower in aged mice of &#62;2 years old (Figure 1C). The total number of ventricular myocytes obtained per adult heart using this protocol was approximately 3 x 106 cells, which was similar to the value previously reported7,12. The action potentials recorded in the ventricular and atrial myocytes (Figure 1D) were similar to those in cells obtained by the Langendorff-based method10. An immunostaining analysis confirmed that the sarcomeric structure of the ventricular myocytes was well-organized with a clearly visible cell membrane (Figure 2A). The individual cardiomyocytes isolated with this method can be directly used in experiments, such as an electrophysiological analysis10 or immunostaining experiment.
Cardiac fibroblasts exist in interstitial spaces. Sufficient digestion of the extracellular matrix results in the isolation of those cells. The isolated cardiac fibroblasts proliferate under culture conditions and can be passaged several times or stored in liquid nitrogen in an appropriate cell reservoir solution. Figure 2B shows that most of the cultured cardiac fibroblasts had transformed into myofibroblasts during subculture, as confirmed by the increased expression of &#945;-smooth muscle actin13,14. Also, the cardiac progenitors can be isolated with the present method and cultured in appropriate culture medium, which start beating automatically10,15.
Homogenization of the robust myocardium is not easy, especially for cardiac tissue from aged mice, which possesses a large amount of extracellular fibers. After antegrade perfusion, protein from the atria and ventricles can be easily homogenized in the lysis buffer with light force to extract proteins. A Western blot analysis demonstrated the specific expression of ANP in atria but not in ventricles from adult (20 weeks old) and aged (108 weeks old) mice (Figure 3).
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/61866/61866fig1.jpg" /> 
Figure&#160;1. Isolated cardiomyocytes from mice.&#160;A. Ventricular myocytes freshly isolated with the antegrade perfusion, with images acquired with low magnification. After the final washing, the cardiomyocytes were resuspended with 2 mL of cell resuspension solution, 100 &#181;L of which was dropped onto the glass-bottom culture dish and cell settlement awaited. Bar, 100 &#181;m. B. Enlarged images of isolated ventricular myocytes (upper) and atrial myocytes (lower). Bar, 100 &#181;m. C. Isolated cells were suspended in the cell resuspension solution and stored at 37&#176;C for the desired period, and the number of live ventricular myocytes was counted in 10-15 fields under a microscope. Rounded cells were considered to have been irreversibly injured or dead16. Green, blue and red symbols were obtained from 3 mice at 8-10 weeks old, and black symbols were from 106 weeks old mouse. Yellow symbol indicates the mean of each group. D. Representative action potentials recorded from ventricular (black) and atrial (red) myocytes of 8-10 mice. The data were obtained from the cells approximately 3 h after isolation. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/61866/61866fig1large.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/61866/61866fig2.jpg" /> 
Figure&#160;2. Immunostaining for &#945;-actinin in isolated mouse ventricular myocytes and &#945;-smooth muscle actin in cultured mouse cardiac fibroblasts.&#160;A. Confocal laser scanning microscopy of immunostaining for &#945;-actinin (green), DAPI staining for nuclei (blue) and a DIC image of ventricular myocytes isolated from mouse heart with antegrade perfusion. Bar, 50 &#181;m. B. Immunostaining for &#945;-smooth muscle actin (green), DAPI staining for nuclei (blue) and a DIC image of cardiac fibroblasts isolated from mouse heart with antegrade perfusion. Cardiac fibroblasts were cultured for four days. Bar, 100 &#181;m. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/61866/61866fig2large.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/61866/61866fig3.jpg" /> 
Figure&#160;3. Western blot analyses of ANP in atria and ventricles.&#160;Western blot analyses for the atrial marker atrial natriuretic peptide (ANP) in atria (A) and ventricles (V) prepared from adult (20 weeks) and aged (108 weeks) hearts. ANP is present in the atria but absent in the ventricles. Use glyceraldehyde 3-phosphate dehydrogenase (GAPDH) as a control house-keeping protein. <a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/61866/61866fig3large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td colspan="2">Stock solutions for isolating heart cells</td>
		</tr>
		<tr>
			<td colspan="2">10X CIB (500 mL)</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>37.99 g</td>
		</tr>
		<tr>
			<td>KCI</td>
			<td>2.01 g</td>
		</tr>
		<tr>
			<td>1 M MgCl2</td>
			<td>2.5 mL</td>
		</tr>
		<tr>
			<td>NaH2PO4</td>
			<td>0.23 g</td>
		</tr>
		<tr>
			<td>HEPES&#160;</td>
			<td>29.79 g</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>Fill up to 500 mL</td>
		</tr>
		<tr>
			<td colspan="2">100 mM CaCl2 stock soution</td>
		</tr>
		<tr>
			<td>CaCl2&#160;</td>
			<td>100 mM</td>
		</tr>
		<tr>
			<td colspan="2">400 mM EGTA stock solution</td>
		</tr>
		<tr>
			<td>EGTA</td>
			<td>400 mM</td>
		</tr>
		<tr>
			<td colspan="2">Insulin solution</td>
		</tr>
		<tr>
			<td>Insulin</td>
			<td>1 unit/mL in 0.1 M HCl</td>
		</tr>
		<tr>
			<td colspan="2">50X Antibiotics stock solution (20 mL)</td>
		</tr>
		<tr>
			<td>Penicillin</td>
			<td>100 mg</td>
		</tr>
		<tr>
			<td>Streptomycin</td>
			<td>100 mg</td>
		</tr>
		<tr>
			<td>Phenol red</td>
			<td>1.5 g</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>20 mL and sterilize with filtering</td>
		</tr>
		<tr>
			<td colspan="2">10X Tyrode solution (1000 mL)</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>81.82 g</td>
		</tr>
		<tr>
			<td>KCl</td>
			<td>4.03 g</td>
		</tr>
		<tr>
			<td>1 M MgCl2</td>
			<td>5 mL</td>
		</tr>
		<tr>
			<td>NaH2PO4</td>
			<td>0.47 g</td>
		</tr>
		<tr>
			<td>HEPES&#160;</td>
			<td>11.92 g</td>
		</tr>
		<tr>
			<td>NaOH</td>
			<td>0.8 g</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>Fill up to 1000 mL</td>
		</tr>
		<tr>
			<td colspan="2">Stock solutin for immunostaining</td>
		</tr>
		<tr>
			<td colspan="2">DAPI stock</td>
		</tr>
		<tr>
			<td>DAPI</td>
			<td>2 mg/mL in methanol</td>
		</tr>
		<tr>
			<td colspan="2">Stock solutions for Western blots</td>
		</tr>
		<tr>
			<td colspan="2">&#160;HEPES buffer (100 mL)</td>
		</tr>
		<tr>
			<td>NaCl</td>
			<td>0.88 g</td>
		</tr>
		<tr>
			<td>400 mM EGTA</td>
			<td>0.25 mL</td>
		</tr>
		<tr>
			<td>HEPES&#160;</td>
			<td>0.24 g</td>
		</tr>
		<tr>
			<td>1M NaOH</td>
			<td>adjust pH to 7.4</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>Fill up to 500 mL</td>
		</tr>
		<tr>
			<td colspan="2">Protease inhibitors cocktail&#160;</td>
		</tr>
		<tr>
			<td>Complete mini</td>
			<td>1 tablet</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>0.4 mL</td>
		</tr>
	</tbody>
</table>
Table 1. Description of the stock solutions.&#160;Keep stock solutions at 4 &#176;C. Aliquot protease inhibitors cocktail for storage at -20 &#176;C.
<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td colspan="2">Solutions for isoltaing heart cells</td>
		</tr>
		<tr>
			<td colspan="2">CIB (200 mL)</td>
		</tr>
		<tr>
			<td>10X CIB</td>
			<td>20 mL</td>
		</tr>
		<tr>
			<td>Insulin solution</td>
			<td>0.01 mL</td>
		</tr>
		<tr>
			<td>Glucose</td>
			<td>0.79 g</td>
		</tr>
		<tr>
			<td>1M NaOH</td>
			<td>pH adjust to 7.4</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>Fill up to 200 mL</td>
		</tr>
		<tr>
			<td colspan="2">Enzyme-mix solution (30 mL)</td>
		</tr>
		<tr>
			<td>Collagenase type2</td>
			<td>30 mg</td>
		</tr>
		<tr>
			<td>Trypsin</td>
			<td>1.8 mg</td>
		</tr>
		<tr>
			<td>Protease</td>
			<td>1.8 mg</td>
		</tr>
		<tr>
			<td>100 mM CaCl2 stock solution</td>
			<td>0.09 mL</td>
		</tr>
		<tr>
			<td>CIB</td>
			<td>30 mL</td>
		</tr>
		<tr>
			<td colspan="2">CIB-Ca2+-BSA (15 mL)</td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>30 mg</td>
		</tr>
		<tr>
			<td>100 mM CaCl2 stock solution</td>
			<td>0.18 mL</td>
		</tr>
		<tr>
			<td>CIB</td>
			<td>15 mL</td>
		</tr>
		<tr>
			<td colspan="2">CIB-EGTA (150 mL)</td>
		</tr>
		<tr>
			<td>400 mM EGTA stock solution</td>
			<td>0.150 mL</td>
		</tr>
		<tr>
			<td>CIB</td>
			<td>150 mL</td>
		</tr>
		<tr>
			<td colspan="2">Tyrode solution (1000 mL)</td>
		</tr>
		<tr>
			<td>10X Tyrode stock solution</td>
			<td>100 mL</td>
		</tr>
		<tr>
			<td>Glucose&#160;</td>
			<td>0.99 g</td>
		</tr>
		<tr>
			<td>1M CaCl2</td>
			<td>1.8 mL</td>
		</tr>
		<tr>
			<td>1M NaOH</td>
			<td>pH adjust to 7.4</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>Fill up to 1000&#160; mL</td>
		</tr>
		<tr>
			<td colspan="2">Cell resuspension solution (15 mL)</td>
		</tr>
		<tr>
			<td>BSA</td>
			<td>30 mg</td>
		</tr>
		<tr>
			<td>50X Antibiotics stock solution</td>
			<td>0.3 mL</td>
		</tr>
		<tr>
			<td>Tyrode solution</td>
			<td>15 mL</td>
		</tr>
		<tr>
			<td colspan="2">Solutions for immunostaining</td>
		</tr>
		<tr>
			<td colspan="2">Cell adherent solution (0.3 mL)</td>
		</tr>
		<tr>
			<td>Cell-Tak</td>
			<td>0.01 mL</td>
		</tr>
		<tr>
			<td>0.1 M NaHCO3 (pH8.0)</td>
			<td>0.285 mL</td>
		</tr>
		<tr>
			<td>0.1 M NaOH</td>
			<td>0.005 mL</td>
		</tr>
		<tr>
			<td colspan="2">Blocking-permeabilizatin solution (10 mL)</td>
		</tr>
		<tr>
			<td>Fetal bovine serum</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>Triton X-100</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>10X PBS</td>
			<td>1 mL</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>7 mL</td>
		</tr>
		<tr>
			<td colspan="2">K+ rich pipette solution</td>
		</tr>
		<tr>
			<td>Potassium aspartate</td>
			<td>70 mM</td>
		</tr>
		<tr>
			<td>KCl</td>
			<td>50 mM</td>
		</tr>
		<tr>
			<td>KH2PO4</td>
			<td>10 mM</td>
		</tr>
		<tr>
			<td>MgSO4</td>
			<td>1 mM</td>
		</tr>
		<tr>
			<td>ATP disodium salt</td>
			<td>3 mM</td>
		</tr>
		<tr>
			<td>GTP lithium salt</td>
			<td>0.1 mM</td>
		</tr>
		<tr>
			<td>EGTA</td>
			<td>5 mM</td>
		</tr>
		<tr>
			<td>HEPES</td>
			<td>5 mM</td>
		</tr>
		<tr>
			<td>KOH</td>
			<td>pH adjust to 7.2</td>
		</tr>
		<tr>
			<td colspan="2">Solutions for Western blots</td>
		</tr>
		<tr>
			<td colspan="2">Lysis buffer (1 mL)</td>
		</tr>
		<tr>
			<td>HEPES buffer</td>
			<td>0.86 mL</td>
		</tr>
		<tr>
			<td>Nonidet-P40</td>
			<td>0.1 mL</td>
		</tr>
		<tr>
			<td>Protease inhibitors cocktail</td>
			<td>0.04 mL</td>
		</tr>
		<tr>
			<td colspan="2">Runnning buffer (1000 mL)</td>
		</tr>
		<tr>
			<td>10X TG (0.25 M Tris and 1.92 M Glycine)</td>
			<td>100 mL</td>
		</tr>
		<tr>
			<td>SDS</td>
			<td>1 g</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>900 mL</td>
		</tr>
		<tr>
			<td colspan="2">Transfer buffer (1000 mL)</td>
		</tr>
		<tr>
			<td>10X TG</td>
			<td>100 mL</td>
		</tr>
		<tr>
			<td>Methanol</td>
			<td>200 mL</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>700 mL</td>
		</tr>
		<tr>
			<td colspan="2">Blotting buffer (TBST)&#160; (1000 mL)</td>
		</tr>
		<tr>
			<td>5M NaCl</td>
			<td>20 mL</td>
		</tr>
		<tr>
			<td>2M Tris-HCl (pH 7.5)</td>
			<td>5 mL</td>
		</tr>
		<tr>
			<td>10% Tween 20</td>
			<td>10 mL</td>
		</tr>
		<tr>
			<td>DW</td>
			<td>965 mL</td>
		</tr>
	</tbody>
</table>
Table 2. Description of the working solutions for isolating heart cells, immunostaining and Western blotting.&#160;Prepare all working solutions just before the experiments.
Supplementary Figure&#160;1. Outline of the cell isolation.&#160;Flow diagram of the isolation of ventricular and atrial myocytes and cardiac fibroblasts from a single heart.&#160;<a href="https://jove.unicartagenaproxy.elogim.com/files/ftp_upload/61866/SupplementaryFig1R.pdf" target="_blank">Please click here to download this figure.</a>

Watch this Scientific Journal Video about An Antegrade Perfusion Method for Cardiomyocyte Isolation from Mice at JoVE.com

An Antegrade Perfusion Method for Cardiomyocyte Isolation from Mice

We developed a simple method for isolating high quality individual mouse heart cells by the antegrade perfusion technique. This method is Langendorff-free and useful for isolating ventricular and atrial myocytes or interstitial cells, such as cardiac fibroblasts or progenitors.

In basic research using mouse heart, isolating viable individual cardiomyocytes is a crucial technical step to overcome. Traditionally, isolating ...

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Universidad de Cartagena UDEC

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JoVE Journal

Biology

10.4K Views.  Shiga University of Medical Science. We developed a simple method for isolating high quality individual mouse heart cells by the antegrade perfusion technique. This method is Langendorff-free and useful for isolating ventricular and atrial myocytes or interstitial cells, such as cardiac fibroblasts or progenitors.

Video: An Antegrade Perfusion Method for Cardiomyocyte Isolation from Mice

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 ...

Medicine

Modifications of the Langendorff Method for Simultaneous Isolation of Atrial and Ventricular Myocytes from Adult Mice

A single cardiomyocyte is a vital tool in the cellular and subcellular level studies of cardiac biology and diseases as a fundamental unit of contraction and electrical activity. Hence, isolating viable, high-quality cardiomyocytes from the heart is the initial and most crucial experimental step. Comparing the various protocols for isolating the cardiomyocytes of adult mice, the Langendorff retrograde perfusion is the most successful and reproducible method reported in the literature, especially for isolating ventricular myocytes. However, isolating quality atrial myocytes from the perfused heart remains challenging, and few successful isolation reports are available. Solving this complicated problem is extremely important because apart from ventricular disease, atrial disease accounts for a large part of heart diseases. Therefore, further investigations on the cellular level to reveal the mechanisms are warranted. In this paper, a protocol based on the Langendorff retrograde perfusion method is introduced and some modifications in the depth of aorta cannulation and the steps that may affect the digestion process to isolate atrial and ventricular myocytes were simultaneously made. Moreover, the isolated cardiomyocytes are confirmed to be amenable to patch clamp investigation.

This protocol describes modifications of the Langendorff method including the depth of aorta cannulation for simultaneous Isolation of atrial and ventricular myocytes from adult mice.

A single cardiomyocyte is a vital tool in the cellular and subcellular level studies of cardiac biology and diseases as a fundamental unit of contraction ...

Isolation, Culture and Transduction of Adult Mouse Cardiomyocytes

Cultured cardiomyocytes can be used to study cardiomyocyte biology using techniques that are complementary to in vivo systems. For example, the purity and accessibility of in vitro culture enables fine control over biochemical analyses, live imaging, and electrophysiology. Long-term culture of cardiomyocytes offers access to additional experimental approaches that cannot be completed in short term cultures. For example, the in vitro investigation of dedifferentiation, cell cycle re-entry, and cell division has thus far largely been restricted to rat cardiomyocytes, which appear to be more robust in long-term culture. However, the availability of a rich toolset of transgenic mouse lines and well-developed disease models make mouse systems attractive for cardiac research. Although several reports exist of adult mouse cardiomyocyte isolation, few studies demonstrate their long-term culture. Presented here, is a step-by-step method for the isolation and long-term culture of adult mouse cardiomyocytes. First, retrograde Langendorff perfusion is used to efficiently digest the heart with proteases, followed by gravity sedimentation purification. After a period of dedifferentiation following isolation, the cells gradually attach to the culture and can be cultured for weeks. Adenovirus cell lysate is used to efficiently transduce the isolated cardiomyocytes. These methods provide a simple, yet powerful model system to study cardiac biology.

This protocol describes a step-by-step method for the reproducible isolation and long-term culture of adult mouse cardiomyocytes with high yield, purity, and viability.

Cultured cardiomyocytes can be used to study cardiomyocyte biology using techniques that are complementary to in vivo systems. For example, the purity and ...

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 ...

Preparation of a Non-Cardiomyocyte Cell Suspension for Single-Cell RNA Sequencing from a Post-Myocardial Infarction Adult Mouse Heart

Myocardial infarction (MI) is one of the most common cardiovascular diseases, with increasing mortality worldwide. Non-cardiomyocytes account for more than half of the total cardiac cell population, and they contribute to adaptive compensations upon myocardial injury, including inflammatory responses, tissue repair, and scar formation. To study the post-MI cardiac microenvironment, single-cell RNA sequencing (scRNA-seq) is widely used to identify different cardiac cell types and intercellular communications. Among the procedures of scRNA-seq sample preparation, preparing the cell suspension is one of the most critical steps, because the cell viability can affect the quality of the scRNA-seq results. Therefore, we designed an experimental protocol for preparing a non-cardiomyocyte cell suspension from post-MI mouse hearts with an extra focus on improving the cell viability by choosing mild digestive enzymes, controlling the digestion time, and applying fluorescence-activated cell sorting (FACS). Finally, we isolated CD45+ cells from the non-cardiomyocyte cell suspension obtained through this protocol, and then we performed scRNA-seq.

Here, we describe a protocol to isolate a sufficient amount of single non-cardiomyocytes with high viability from a post-myocardial infarction (MI) mouse heart. This can be used for subsequent single-cell sequencing, flow cytometry analysis, and primary cell culture.

Myocardial infarction (MI) is one of the most common cardiovascular diseases, with increasing mortality worldwide. Non-cardiomyocytes account for more ...

Isolation, Transfection, and Long-Term Culture of Adult Mouse and Rat Cardiomyocytes

Ex vivo culture of the adult mammalian cardiomyocytes (CMs) presents the most relevant experimental system for the in vitro study of cardiac biology. Adult mammalian CMs are terminally differentiated cells with minimal proliferative capacity. The post-mitotic state of adult CMs not only restricts cardiomyocyte cell cycle progression but also limits the efficient culture of CMs. Moreover, the long-term culture of adult CMs is necessary for many studies, such as CM proliferation and analysis of gene expression.
The mouse and the rat are the two most preferred laboratory animals to be used for cardiomyocyte isolation. While the long-term culture of rat CMs is possible, adult mouse CMs are susceptible to death and cannot be cultured more than five days under normal conditions. Therefore, there is a critical need to optimize the cell isolation and long-term culture protocol for adult murine CMs. With this modified protocol, it is possible to successfully isolate and culture both adult mouse and rat CMs for more than 20 days. Moreover, the siRNA transfection efficiency of isolated CM is significantly increased compared to previous reports. For adult mouse CM isolation, the Langendorff perfusion method is utilized with an optimal enzyme solution and sufficient time for complete extracellular matrix dissociation. In order to obtain pure ventricular CMs, both atria were dissected and discarded before proceeding with the disassociation and plating. Cells were dispersed on a laminin coated plate, which allowed for efficient and rapid attachment. CMs were allowed to settle for 4-6 h before siRNA transfection. Culture media was refreshed every 24 h for 20 days, and subsequently, CMs were fixed and stained for cardiac-specific markers such as Troponin and markers of cell cycle such as KI67.

Here, we present a protocol for the isolation, transfection, and long-term culture of adult mouse and rat cardiomyocytes.

Ex vivo culture of the adult mammalian cardiomyocytes (CMs) presents the most relevant experimental system for the in vitro study of cardiac biology. ...

Simultaneous Isolation and Culture of Atrial Myocytes, Ventricular Myocytes, and Non-Myocytes from an Adult Mouse Heart

The isolation and culturing of cardiac myocytes from mice has been essential for furthering the understanding of cardiac physiology and pathophysiology. While isolating myocytes from neonatal mouse hearts is relatively straightforward, myocytes from the adult murine heart are preferred. This is because compared to neonatal cells, adult myocytes more accurately recapitulate cell function as it occurs in the adult heart in vivo. However, it is technically difficult to isolate adult mouse cardiac myocytes in the necessary quantities and viability, which contributes to an experimental impasse. Furthermore, published procedures are specific for the isolation of either atrial or ventricular myocytes at the expense of atrial and ventricular non-myocyte cells. Described here is a detailed method for isolating both atrial and ventricular cardiac myocytes, along with atrial and ventricular non-myocytes, simultaneously from a single mouse heart. Also provided are the details for optimal cell-specific culturing methods, which enhance cell viability and function. This protocol aims not only to expedite the process of adult murine cardiac cell isolation, but also to increase the yield and viability of cells for investigations of atrial and ventricular cardiac cells.

A method is described for the simultaneous isolation of myocytes and non-myocytes from both the atria and ventricles of a single adult mouse heart. This protocol results in consistent yields of highly viable cardiac myocytes and non-myocytes and details optimal cell-specific culture conditions for phenotyping and in vitro analysis.

The isolation and culturing of cardiac myocytes from mice has been essential for furthering the understanding of cardiac physiology and pathophysiology. ...

Isolation of High Quality Murine Atrial and Ventricular Myocytes for Simultaneous Measurements of Ca2+ Transients and L-Type Calcium Current

Mouse models play a crucial role in arrhythmia research and allow studying key mechanisms of arrhythmogenesis including altered ion channel function and calcium handling. For this purpose, atrial or ventricular cardiomyocytes of high quality are necessary to perform patch-clamp measurements or to explore calcium handling abnormalities. However, the limited yield of high-quality cardiomyocytes obtained by current isolation protocols does not allow both measurements in the same mouse. This article describes a method to isolate high-quality murine atrial and ventricular myocytes via retrograde enzyme-based Langendorff perfusion, for subsequent simultaneous measurements of calcium transients and L-type calcium current from one animal. Mouse hearts are obtained, and the aorta is rapidly cannulated to remove blood. Hearts are then initially perfused with a calcium-free solution (37 &#176;C) to dissociate the tissue at the level of intercalated discs and afterwards with an enzyme solution containing little calcium to disrupt extracellular matrix (37 &#176;C). The digested heart is subsequently dissected into atria and ventricles. Tissue samples are chopped into small pieces and dissolved by carefully pipetting up and down. The enzymatic digestion is stopped, and cells are stepwise reintroduced to physiologic calcium concentrations. After loading with a fluorescent Ca2+-indicator, isolated cardiomyocytes are prepared for simultaneous measurement of calcium currents and transients. Additionally, isolation pitfalls are discussed and patch-clamp protocols and representative traces of L-type calcium currents with simultaneous calcium transient measurements in atrial and ventricular murine myocytes isolated as described above are provided.

Isolation of High Quality Murine Atrial and Ventricular Myocytes for Simultaneous Measurements of Ca2+ Transients and L-Type Calcium Current

Mouse models allow studying key mechanisms of arrhythmogenesis. For this purpose, high quality cardiomyocytes are necessary to perform patch-clamp measurements. Here, a method to isolate murine atrial and ventricular myocytes via retrograde enzyme-based Langendorff perfusion, which allows simultaneous measurements of calcium-transients and L-type calcium current, is described.

Mouse models play a crucial role in arrhythmia research and allow studying key mechanisms of arrhythmogenesis including altered ion channel function and ...

Langendorff Retrograde Heart Perfusion: An Ex Vivo Technique to Perfuse Isolated Mouse Heart

Source: Wu, K. et al. <a href="https://jove.unicartagenaproxy.elogim.com/video/62514" target="_blank">Modifications of the Langendorff Method for Simultaneous Isolation of Atrial and Ventricular Myocytes from Adult Mice</a>. J. Vis. Exp. (2021)
In this video, we perform Langendorff retrograde perfusion of an isolated mouse heart. During the procedure, the cardiac activity of the heart is maintained by perfusing it retrogradely with a perfusion solution via the coronary arteries using a cannula inserted into the ascending aorta. The model is used to study the cardiac pathophysiology of the heart.

Wsteczna perfuzja serca Langendorffa: technika ex vivo perfuzji izolowanego serca myszy

Source: Wu, K. et al. Modifications of the Langendorff Method for Simultaneous Isolation of Atrial and Ventricular Myocytes from Adult Mice. J. Vis. Exp. ...