Name: Fabrication of Biologically Derived Injectable Materials for Myocardial Tissue Engineering (Video) | JoVE Journal
Uploaded: 2010-12-20T15:00:00.000+00:00
Duration: 11 min 32 s
Description: Learn to fabricate injectable matrix gels from decellularized pericardial tissue for cardiac tissue engineering. This method demonstrates in vivo scaffold formation and vascular cell infiltration in rat myocardium.

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5 minutes

This research was supported in part by the NIH Director's New Innovator Award Program, part of the NIH Roadmap for Medical Research, through grant number 1-DP2-OD004309-01. S.B.S-N. would like to thank the NSF for a Graduate Research Fellowship.

1. Pre-processing Tissue Preparation
<ol class="lalpha">
<li>	Before using this protocol, one must have already decellularized the tissue of choice. For this example, fresh porcine and human pericardium samples are decellularized using hypotonic and hypertonic rinses in deionized (DI) water and sodium dodecyl sulfate (SDS).</li>
<li>	Specifically, first wash the porcine pericardium in DI water for 30 minutes, then stir continuously in 1% SDS in phosphate buffered saline (PBS) for 24 hours, followed by a 5 hour DI water rinse. For human pericardia, first rinse in DI water for 30 minutes, then stir continuously in 1% SDS in PBS for 60-65 hours, followed by an overnight DI rinse. Remove all specimens from their final solution and rinse again under running DI water 1. </li>
<li>	To verify decellularization, remove a small piece, fresh freeze it in O.C.T. freezing medium, and take 10 μm tissue sections every 100 μm throughout the sample for examination via histological analysis, as previously reported 34-36.</li>
<li>	Use hematoxylin and eosin (H&amp;E) stains to examine the tissue for the absence of nuclei. One could also use a fluorescent Hoescht 33342 stain (1.0 μg/mL) for DNA to verify the H&amp;E results; briefly, fix the sections, rehydrate and rinse in water, stain for 10 minutes, and then rinse well and store in the dark. Alternatively, one can use a kit such as the Qiagen DNeasy Blood and Tissue kit, which is designed to quantify the total DNA content of a sample.</li>
</ol>
2. Preparation of Injectable ECM
<ol class="lalpha">
<li>	Lyophilization
<ol class="lroman">
<li>	After appropriate preparation, freeze the decellularized samples with liquid nitrogen or by storing at -80 °C. Lyophilize the samples until completely dry. Depending on your system and the water content of your samples, this may take anywhere from 12 to 72 hours.</li>
</ol>
</li>
<li>	Milling
<ol class="lroman">
<li>	Once completely dry, a Wiley Mini Mill is used to grind the dry ECM into a fine powder. Choose the appropriate sieve size for your purposes; here, the 40 gauge mesh is used. Once the majority of the sample has come through the filter, remove the collection jar with the milled ECM powder. If there is only a small sample, the rest of the sample can be extracted from the mill in a variety of ways; here, a Q-tip is used to remove the ECM stuck behind the stationary blades of the mill.</li>
<li>	Always make sure that the mill is clean and free of debris. It is also important to make sure that both the mill and your sample are totally dry; any remaining moisture will cause the ECM to aggregate and clump together, preventing successful milling. The ECM may pick up moisture from the air and so should go directly from the lyophilizer to the mill.</li>
</ol>
</li>
<li>	Digestion
<ol class="lroman">
<li>	To form the injectable ECM, the powder is digested pepsin. The following protocol was modified from Freyetes, et al. (2).</li>
<li>	It is important to maintain as sterile a product as possible, as it will be injected in vivo and contamination may cause complications. Thus, use sterile vials and weigh spoons and filter all solutions before use. A lyophilization step after milling and before digestion will also help maintain sterility.</li>
<li>	Weigh out the desired amount of ECM powder into an appropriate scintillation vial. For total volumes smaller than 1 mL, it is recommended you use a 2 mL vial and for larger volumes, a 20 mL vial. This ensures that there is enough liquid in the bottom of the vial to stir effectively.</li>
<li>	Weigh out the desired amount of pepsin into a scintillation vial. Add 0.1 M HCl such that the pepsin is at a concentration of 1 mg/mL. Make sure the pepsin is fully dissolved (no particulates) before use this can be hastened by vortexing the pepsin solution.</li>
<li>	Add the pepsin/HCl solution to the scintillation vial with the ECM powder so that the ECM is at a concentration of 10 mg/mL.</li>
<li>	Stir solution continuously for 60-65 hours, periodically scraping down the sides of the vial with a weigh spoon or spatula.</li>
</ol>
</li>
<li>	pH Adjustment
<ol class="lroman">
<li>	This step is performed to bring the liquid matrix material to physiological pH and to inactivate the pepsin, keeping it from cleaving the ECM further. Again, be sure to use filtered solutions made with Millipore water.</li>
<li>	1 M NaOH is added to be 1/10 the original volume. Test the pH at this point and add small amounts (2-10 μl) of NaOH or HCl such that the desired pH (7.4) is reached. Keep track of all small amounts added for neutralization or removed for pH testing. Once the solution has been neutralized, add 10x PBS to be 1/10 the final volume (1/9 the current volume). Determine the concentration of the injectable ECM and then add 1x PBS to reach desired final concentration, here 6 mg/mL.</li>
<li>	Characterization of the injectable ECM can be done via SDS-PAGE, Blyscan Colorimetric GAG Assay, and mass spectroscopy.</li>
<li>	At this point, the matrix material can be injected in vivo to form a scaffold for myocardial tissue engineering.</li>
</ol>
</li> 
<li>	Biotin-Labeling
<ol class="lroman">
<li>	The ECM can be tagged with biotin before injection for easy visualization of the injected ECM.</li>
<li>	Prepare a 10mM solution of Biotin and add to the injectable ECM at a ratio of 0.3mg/mg. The ECM should be at the desired concentration for injection. If injecting at a concentration of 6 mg/mL, add 40 μL Biotin per 1 mL of ECM. Prior to injection, keep the biotin-ECM solution on ice for at least 1 hour.</li>
</ol>
</li>
<li>	All processing steps can be performed at room temperature. To keep the injectable matrix from gelling, the pH adjustment step may be done on ice. </li>
</ol>
3. Myocardial Injections
<ol class="lalpha">
<li>Injection preparation
<ol class="lroman">
<li>For the female rats (225-250 g) used here, 75 μL injections of pH 7.4 injectable ECM were prepared in 0.1 mL syringes tipped with 30 gauge needles. If male rats (375-400 g) were used, 90 μL could be injected.</li>
<li>All surgical supplies should be sterilized prior to surgery; here we use an autoclaved surgical pack that contains all the necessary tools.</li>
</ol>
</li>
<li>On the day of surgery, a Harlan Sprague-Dawley rat is anesthetized using isoflurane at 5%, intubated using an otoscope, and then maintained at 2.5% isoflurane throughout the procedure.</li>
<li>Add artificial tear ointment to the animal's eyes to protect against dryness and hair. Administer 3 mL of Lactated Ringers solution for hydration during surgery. This should be done via subcutaneous injection in the lower abdominal area.</li>
<li>Place the animal in supine position on the surgical table and gently tape down limbs. Use clippers to remove the hair on the abdomen and vacuum free hair prior to scrubbing.</li>
<li>Make a series of small injections (approximately 50 μL each) of 2% lidocaine along a diagonal from the zyphoid process to the lower right-hand side of the abdomen. Then scrub three times with betadine, starting in the middle and moving outward. Repeat with 70% ethanol. Cover the animal using a surgical drape with a pre-made circular window; secure with towel clamps, if necessary.</li>
<li>Using a No. 10 scalpel make a 3-4 cm incision from the xyphoid process to the lower right-hand side of the abdomen. Locate xyphoid process and dissect vertically down through the muscle to the right, being careful to avoid the large vessel on the right. Once you have dissected through the muscle, use scissors to cut laterally through the muscle, exposing the diaphragm. Be careful to avoid the liver.</li>
<li>Using a 36 inch length of 3-0 Vicrile suture and a pair of hemostats, drive one needle through the zyphoid process and pull the suture halfway through. Tape the ends of the suture together and fix that to a point above and behind the animal essentially lifting the zyphoid up and exposing the diaphragm. With another 36 inch length of 3-0 Vicrile suture, drive a needle through the muscle closest to the xyphoid process and, again, pull through and fix the ends to another point to the right of the surgical table, fully exposing the surgical cavity.</li>
<li>At this point, you should be able to see the heart through the diaphragm. Using a small pair of rat tooth microforceps, grab the center of diaphragm, pull it out toward you and make a very small incision with blunt scissors. It is extremely important to use very blunt scissors in order to avoid poking the lungs. Once this hole has been made, the lungs will retract, allowing you to make a 2-3 cm incision vertically through the diaphragm to visualize the heart.</li>
<li>Insert a 3-inch Q-tip to the left of the cavity to push the lungs out of the way. Use a towel clamp to secure the Q-tip in place. Use another Q-tip to move the right lung out of the way in order to locate the pericardial sac. Using a pair of microforceps and a pair of large serrated forceps, tear through the pericardial sac, exposing the apex of the heart. If the animal has previously undergone an infarction procedure, the pericardium will already be absent.</li>
<li>Grab the apex of the heart with the rat tooth microforceps and inject the liquid matrix material a third of the way up from the apex. Insert the needle parallel to the epicardial surface and inject with the beveled edge of the needle to the left. Be sure to avoid the great cardiac vein. Wait a couple seconds before removing the needle. You should see a whitening of the tissue at the site of injection.</li>
<li>Clean up blood in the cavity and remove the towel clamp and Q-tip that was holding the right lung. Use curved microhemostats and the rat tooth microforceps to close the diaphragm. Make an initial knot and then use the serrated forceps and microhemostats to close the diaphragm with a continuous suture and a tapered needle. Before closing entirely, insert PE160 suction tubing and use a 10 mL syringe to evacuate the chest cavity as the suture is tightened.</li>
<li>When properly evacuated and closed, the diaphragm should be concave. A convex diaphragm indicates that there is still air in the cavity.</li>
<li>At this point the isoflurane can be turned down to 1%.</li>
<li>Take out both 3-0 Vicrile sutures holding the cavity open. Use sterile water to hydrate the muscle, wiping excess away with a Q-tip or sterile gauze. Use a new length of 3-0 suture to close the muscle layer with intermittent sutures.</li>
<li>At this point, the isoflurane can be turned off.</li>
<li>Clean area with sterile water and use staples to close skin. If staples will interfere with the study, 5-0 proline suture can also be used. In that case, use a reverse cutting (RC) needle to close the skin with intermittent sutures. In both cases, spot surgical glue over the closed incision.</li>
<li>Use a Q-tip to anoint the incision site with a triple-antibiotic ointment.</li>
<li>Allow the animal to recover under 100% oxygen.</li>
<li>When the animals starts to breathe around the ventilator, remove the trachea tube.</li>
<li>Once the animals are sternal, administer a subcutaneous injection of 0.05 mg/kg of buprenorphine hydrochloride and return them to their home cage on a sterile towel.</li>
<li>The animals should receive post-operative observation and care.</li>
<li>At the time points of interest, the animals are euthanized and the hearts removed for analysis. Short axis cross sections are taken and can be stained with hematoxylin and eosin (H&amp;E) for gross tissue analysis. At short time points, the injected region will appear as a pink, fibrous network that has spread interstitially. At later time points, one will observe an influx of cells and an eventual degradation of the injected matrix after 2 to 3 weeks. If the ECM was labeled with biotin before injecting, it can be more directly visualized by staining the biotin with HRP-conjugated streptavidin. Immunohistochemical staining can be used to identify specific cells or structures in the injection region, here the slides have been co-stained with a FITC-conjugated isolectin that binds to endothelial cells and fluoresces green and an anti-smooth muscle actin antibody with an Alexafluor secondary antibody that reports the SMCs in red.</li>
</ol>
4. Representative Results
Previous characterization of matrix materials prepared in this way demonstrated the retention of a variety of macromolecules. Specifically, multiple fibrous proteins and glycoproteins were identified via mass spectrometry (Table 1). If the matrix materials processed according to this protocol are found to no longer contain a complex array of macromolecules, it could be that the decellularization protocol employed is too harsh. Once fully lyophilized, the dried pericardial ECM looks like very stiff, crumpled paper. Other tissue types will resemble packing peanuts. If milled well, the ECM should fall through the sieve and be collected in the jar at the bottom. If there is moisture left in the sample, the ECM will clump together and get stuck in the milling chamber. After digestion, the ECM solution should be a milky color and completely free of visible particulates. It will also be slightly more viscous than the HCl alone. If the ECM does not digest well, there will still be large particulates in the vial; alternatively, the ECM may crash out of solution. After pH adjustment, there is no visible change in the solution, and the ECM is still a cloudy, homogeneous liquid. If it starts to gel, the viscosity will increase and it will be difficult or impossible to draw the material up into a syringe. If this happens, perform the pH adjustment step on ice, with pre-chilled solutions. Once the injections have been prepared, keep them on ice until use. If the injection is successful, the region around the needle tip whitens and a small bolus is visible. If this is not observed, the injection may have gone into the chamber instead of into the wall. When suturing the animal up after injection, careful closing of the diaphragm is the most important step. If done correctly, the diaphragm will be tight against the lungs and will appear concave. If there is any air left inside the lungs, the diaphragm will remain convex, or have an area where it balloons out. When examining the histology of the injection region at an early time point (30 minutes to 4 hours post-injection), one should see a pink, fibrous area that is devoid of cells this is the reassembled matrix material post-injection (Figure 2). The network often spreads interstitially and may be present throughout many sections. A possible explanation for seeing only a very small area of matrix gel is that a portion of the injection missed the intramural target and was either injected into the LV chamber or leaked out of the injection location. Additionally, depending on the gelation time, the interstitial spread may vary.
<img src="/files/ftp_upload/2109/2109fig1.jpg" alt="SDS-PAGE gel electrophoresis diagram showing protein separation by molecular weight." data-altupdatedat="1788235205000" data-alt="Figure 1"> 
Figure 1. Polyacrylamide gel electrophoresis (PAGE) results. (A) Molecular weight standard. (B) Rat tail collagen Type I (2.5 mg/mL) compared to the solubilized human (C) and porcine (D) pericardial ECM (7 mg/mL). Note the presence of collagen as well as several other proteins and peptides in the pericardial matrix samples.
<img src="/files/ftp_upload/2109/2109table1.jpg" alt="Protein identification table; identified biglycan, collagen, elastin in HPM, PPM samples." data-altupdatedat="1788235205000" data-alt="Table 1"> 
Table 1. ECM components identified with mass spectroscopy.
<img src="/files/ftp_upload/2109/2109fig2.jpg" alt="Histology comparison, microscopy image showing tissue sections A and B, with arrow indicating structures." data-altupdatedat="1788235205000" data-alt="Figure 2"> 
Figure 2. Myocardial injections: in vivo gelation. H&amp;E stain of human (A) and porcine (B) pericardial matrix injections that have gelled in vivo after 45 minutes. Arrows denote matrix location, stained lighter pink than the myocardium. Scale bar is 500 μm.
<img src="/files/ftp_upload/2109/2109fig3.jpg" alt="Fluorescence microscopy images showing cellular protein localization; contrast analysis in tissue sections." data-altupdatedat="1788235205000" data-alt="Figure 3"> 
Figure 3.Vascular cell infiltration. Fluorescent stains for vessels in the injected human (A-C) and porcine (D-F) matrix gels at two weeks. Endothelial cells are labeled green (A, D), while smooth muscle cells are labeled red (B, E). Merged images are shown in C and F. Scale bar is 100 μm. The white dotted lines indicate the area of matrix injection, as determined by H&amp;E analysis of a nearby section.
<img src="/files/ftp_upload/2109/2109fig4.jpg" alt="Fluorescence microscopy images showing cellular localization in tissue sections, with cell nuclei and markers." data-altupdatedat="1788235205000" data-alt="Figure 4"> 
Figure 4. Stem cells within matrix injection region. A Hoescht stain for nuclei (blue) and c-kit (green) identifies stem cells in the human (A) and porcine (B) matrix injection regions. Scale bar is 50 μm.

<ol><li>Seif-Naraghi, S. B., Salvatore, M. A., Magoffin-Schup, P. J., Hu, D. P., Christman, K. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Design+and+characterization+of+an+injectable+pericardial+matrix+gel%3A+A+potentially+autologous+scaffold+for+cardiac+tissue+engineering%5BTitle%5D)+AND+%22Tissue+Engineering%22%5BJournal%5D)">Design and characterization of an injectable pericardial matrix gel: A potentially autologous scaffold for cardiac tissue engineering.</a> Tissue Engineering. , (2009).</li>
<li>Freytes, D. O., Martin, J., Velankar, S. S., Lee, A. S., Badylak, S. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Preparation+and+rheological+characterization+of+a+gel+form+of+the+porcine+urinary+bladder+matrix%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">Preparation and rheological characterization of a gel form of the porcine urinary bladder matrix.</a> Biomaterials. 29, 1630-1630 (2008).</li>
<li>Gilbert, T. W., Sellaro, T. L., Badylak, S. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Decellularization+of+tissues+and+organs%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">Decellularization of tissues and organs.</a> Biomaterials. 27, 3675-3675 (2006).</li>
<li>Liao, J., Joyce, E. M., Sacks, M. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Effects+of+decellularization+on+the+mechanical+and+structural+properties+of+the+porcine+aortic+valve+leaflet%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">Effects of decellularization on the mechanical and structural properties of the porcine aortic valve leaflet.</a> Biomaterials. 29, 1065-1065 (2008).</li>
<li>Singelyn, J. M., DeQuach, J. A., Seif-Naraghi, S. B., Littlefield, R. B., Schup-Magoffin, P. J., Christman, K. L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Naturally+derived+myocardial+matrix+as+an+injectable+scaffold+for+cardiac+tissue+engineering%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">Naturally derived myocardial matrix as an injectable scaffold for cardiac tissue engineering.</a> Biomaterials. 30, 5409-5409 (2009).</li>
<li>Christman, K. L., Vardanian, A. J., Fang, Q., Sievers, R. E., Fok, H. H., Lee, R. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Injectable+fibrin+scaffold+improves+cell+transplant+survival%2C+reduces+infarct+expansion%2C+and+induces+neovasculature+formation+in+ischemic+myocardium%5BTitle%5D)+AND+%22J+Am+Coll+Cardiol%22%5BJournal%5D)">Injectable fibrin scaffold improves cell transplant survival, reduces infarct expansion, and induces neovasculature formation in ischemic myocardium.</a> J Am Coll Cardiol. 44, 654-654 (2004).</li>
<li>Christman, K. L., Fok, H. H., Sievers, R. E., Fang, Q., Lee, R. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Fibrin+glue+alone+and+skeletal+myoblasts+in+a+fibrin+scaffold+preserve+cardiac+function+after+myocardial+infarction%5BTitle%5D)+AND+%22Tissue+Eng%22%5BJournal%5D)">Fibrin glue alone and skeletal myoblasts in a fibrin scaffold preserve cardiac function after myocardial infarction.</a> Tissue Eng. 10, 403-410 (2004).</li>
<li>Huang, N. F., Sievers, R. E., Park, J. S., Fang, Q., Li, S., Lee, R. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((A+rodent+model+of+myocardial+infarction+for+testing+the+efficacy+of+cells+and+polymers+for+myocardial+reconstruction%5BTitle%5D)+AND+%22Nat+Protoc%22%5BJournal%5D)">A rodent model of myocardial infarction for testing the efficacy of cells and polymers for myocardial reconstruction.</a> Nat Protoc. (1), 1596-1609 (2006).</li>
<li>Ott, H. C., Matthiesen, T. S., Goh, S. K., Black, L. D., Kren, S. M., Netoff, T. I. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Perfusion-decellularized+matrix%3A+using+nature%27s+platform+to+engineer+a+bioartificial+heart%5BTitle%5D)+AND+%22Nat+Med%22%5BJournal%5D)">Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart.</a> Nat Med. 14, 213-221 (2008).</li>
<li>Badylak, S. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+extracellular+matrix+as+a+biologic+scaffold+material%5BTitle%5D)+AND+%22Biomaterials%22%5BJournal%5D)">The extracellular matrix as a biologic scaffold material.</a> Biomaterials. 28, 3587-3593 (2007).</li>
</ol>

Animal Use: All experiments in this study were performed in accordance with the guidelines published by the Institutional Animal Care and Use Committee at the University of California, San Diego and the American Association for Accreditation of Laboratory Animal Care.

This method allows for the generation of biologically derived, injectable scaffolds for myocardial tissue engineering. Although these methods were initially developed for the fabrication and in vivo testing of a myocardial matrix gel and presented here with a pericardial matrix gel, this protocol can be adapted for use with any tissue, provided the tissue can be appropriately decellularized. Decellularization should be performed and verified prior to the use of these methods, as the presence of DNA in the matr...

<table><tbody><tr><td>&lt;strong&gt;Reagents:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Pepsin</td><td>Sigma-Aldrich</td><td>p6887-1G</td><td>Lyophilized </td></tr><tr><td>Biotin</td><td>Thermo Fisher Scientific, Inc.</td><td>21217</td><td></td></tr><tr><td>Neutravidin-HRP</td><td>Thomas Scientific</td><td>21130</td><td></td></tr><tr><td>&lt;strong&gt;Equipment:&lt;/strong&gt; </td><td></td><td></td><td></td></tr><tr><td>Wiley Mini Mill</td><td>Thomas Scientific</td><td>3383L10</td><td></td></tr><tr><td>Labconco Lyophilizer</td><td>Labconco Corp.</td><td>7670520</td><td></td></tr><tr><td>&lt;strong&gt;Surgical supplies:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Betadine</td><td>Purdue Products L.P.</td><td>67618-154-16</td><td></td></tr><tr><td>Lactated Ringers Solution</td><td>MWI Veterinary Supply</td><td>003966</td><td></td></tr><tr><td>KY Jelly</td><td>MWI Veterinary Supply</td><td>28658</td><td></td></tr><tr><td>Lidocaine, 2%</td><td>MWI Veterinary Supply</td><td>17767</td><td></td></tr><tr><td>Buprenorphine hydrochloride</td><td>Reckitt Benckiser</td><td>12496-0757-1</td><td></td></tr><tr><td>Artificial tear ointment</td><td>Fisher Scientific</td><td>NC9860843</td><td></td></tr><tr><td>Triple antibiotic ointment</td><td>Fisher Scientific</td><td>19082795</td><td></td></tr><tr><td>Isoflurane</td><td>MWI Veterinary Supply</td><td>60307-120-25</td><td></td></tr><tr><td>Otoscope </td><td>MWI Veterinary Supply</td><td>008699</td><td></td></tr><tr><td>Stop cock</td><td>MWI Veterinary Supply</td><td>006245</td><td></td></tr><tr><td>3-0 Vicrile suture</td><td>MWI Veterinary Supply</td><td>J327H</td><td></td></tr><tr><td>5-0 Proline suture</td><td>MWI Veterinary Supply</td><td>s-1173</td><td></td></tr><tr><td>Reverse cutting (RC) needle</td><td>Ethicon Inc.</td><td>8684G</td><td></td></tr><tr><td>Microhemostats </td><td>Fine Science Tools</td><td>13013-14</td><td></td></tr><tr><td>Rat tooth microforceps</td><td>Fine Science Tools</td><td>11084-07</td><td></td></tr><tr><td>No. 10 scalpel</td><td>Fine Science Tools</td><td>10110-01</td><td></td></tr><tr><td>Blunt scissors</td><td>Fine Science Tools</td><td>14108-09</td><td></td></tr><tr><td>Sharp, curved scissors</td><td>Fine Science Tools</td><td>14085-08</td><td></td></tr><tr><td>Large, serrated forceps</td><td>Fine Science Tools</td><td>1106-12</td><td></td></tr><tr><td>PE160 suction tubing</td><td>BD Biosciences</td><td>427430</td><td></td></tr><tr><td>Clippers </td><td>MWI Veterinary Supply</td><td>21608</td><td></td></tr><tr><td>Skin staples/stapler </td><td>Ethicon Inc.</td><td>PRR35</td><td></td></tr><tr><td>&lt;strong&gt;General supplies:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Stir plates</td><td></td><td></td><td></td></tr><tr><td>0.1 M HCl</td><td></td><td></td><td></td></tr><tr><td>1 M NaOH</td><td></td><td></td><td></td></tr><tr><td>10x PBS</td><td></td><td></td><td></td></tr><tr><td>1x PBS</td><td></td><td></td><td></td></tr><tr><td>70% Ethanol</td><td></td><td></td><td></td></tr><tr><td>0.1 mL syringes</td><td></td><td></td><td></td></tr><tr><td>10 mL syringe</td><td></td><td></td><td></td></tr><tr><td>Q-tips</td><td></td><td></td><td></td></tr><tr><td>Surgical glue</td><td></td><td></td><td></td></tr><tr><td>Surgical drape</td><td></td><td></td><td></td></tr><tr><td>Towel clamps</td><td></td><td></td><td></td></tr><tr><td>Small hand-held vacuum </td><td></td><td></td><td></td></tr></tbody></table>

fabrication of biologically derived injectable materials for myocardial tissue engineering

Fabrication of Biologically Derived Injectable Materials for Myocardial Tissue Engineering

This protocol provides methods for the preparation of an injectable extracellular matrix (ECM) gel for myocardial tissue engineering applications. Briefly, decellularized tissue is lyophilized, milled, enzymatically digested, and then brought to physiological pH. The lyophilization removes all water content from the tissue, resulting in dry ECM that can be ground into a fine powder with a small mill. After milling, the ECM powder is digested with pepsin to form an injectable matrix. After adjustment to pH 7.4, the liquid matrix material can be injected into the myocardium. Results of previous characterization assays have shown that matrix gels produced from decellularized pericardial and myocardial tissue retain native ECM components, including diverse proteins, peptides and glycosaminoglycans. Given the use of this material for tissue engineering, in vivo characterization is especially useful; here, a method for performing an intramural injection into the left ventricular (LV) free wall is presented as a means of analyzing the host response to the matrix gel in a small animal model. Access to the chest cavity is gained through the diaphragm and the injection is made slightly above the apex in the LV free wall. The biologically derived scaffold can be visualized by biotin-labeling before injection and then staining tissue sections with a horse radish peroxidase-conjugated neutravidin and visualizing via diaminobenzidine (DAB) staining. Analysis of the injection region can also be done with histological and immunohistochemical staining. In this way, the previously examined pericardial and myocardial matrix gels were shown to form fibrous, porous networks and promote vessel formation within the injection region.

Methods for preparing an injectable matrix gel from decellularized tissue and injecting it into rat myocardium in vivo are described.

This protocol provides methods for the preparation of an injectable extracellular matrix (ECM) gel for myocardial tissue engineering applications.  ...

Matrix gels produced from decellularized, pericardial and myocardial tissue retain native extracellular matrix components including diverse proteins, peptides, and glycosaminoglycans. These tissue matrixes can be used for tissue engineering. In this video matrix gels are fabricated by decellularizing pericardial tissue to yield acellular extracellular matrix.The extracellular matrix is then processed to create a solubilized liquid version. Next, the solubilized matrix is tested in a small animal model to determine its feasibility as an injectable scaffold. Histological and immunohistochemical analysis demonstrate that in vivo, the injected material forms a porous fibrous scaffold that allows for vascular cell infiltration.Hi, my name is Sonia Zeki. I'm a graduate student in the lab of Dr.Karen Chrisman at the University of California San Diego. Today we will fabricate Solubilized ECM from decellularized tissue and demonstrate in vivo testing for cardiac tissue engineering applications.These techniques are important for the development of an injectable biomaterial therapy for the treatment of heart failure. Post myocardial infarction demonstrating the surgical procedure be Pam, shoot McGuffin, a veterinary neurosurgeon in our laboratory. So let's get started.Begin this protocol by decellularizing the tissue to leave just the extracellular matrix or ECM first place porcine pericardium in a beaker of deionized water and wash it by stirring for 30 minutes at room temperature. After washing, place the tissue in one times PBS containing 1%SDS and 1%penicillin streptomycin stir continuously for 24 hours at room temperature. The next day, return the tissue to deionized water and stir continuously for five hours, shaken a 50 milliliter tube until all suds are gone.Hematin and eoin staining should reveal the absence of nuclei in decellularized tissue. Place the remainder of the decellularized tissue in a 15 to 50 milliliter conical tube. Then place the tissue in the minus 80 degrees Celsius freezer.Lyophilize the frozen samples by freeze drying under very low pressure and very low temperature until completely dry. Depending on the system used and the water content of the samples, this may take anywhere from 12 to 72 hours. Once the decellularized tissue is completely dry, transfer it to a Wiley Minim mill.Set up with a 40 gauge mesh, grind the tissue into a fine powder. Once the majority of the sample has come through the filter, remove the collection jar. This sample is now referred to as extracellular matrix or ECM powder.A second lyophilization step may be performed at this time, if not continuing immediately to the next step. This ensures the accuracy of the recorded weight to solubilize the ECM. Weigh out the desired amount of ECM powder into a sterile ation vial.Add sterile filtered hydrogen chloride solution containing one milligram per milliliter. Pepcid to the scintillation vial with the ECM powder so that the ECM is at a concentration of 10 milligrams per milliliter. Add a stir bar and place the vial on the stir plate.Stir continuously for 48 to 60 hours, periodically scraping down the sides of the vial with a sterile WHE spoon or spatula. To ensure digestion of all the ECM powder. As the ECM is digested, it will go into solution.Once the ECM has been solubilized, place the sample on ice and adjust the pH to 7.4 using sodium hydroxide and hydrochloric acid. Once the pH has been adjusted, add 10 times PBS so that the final sort concentration of the solution is one times PBS. For example, if you have 900 microliters of ECM solution, after pH adjustments, 100 microliters of 10 times PBS should be added.Determine the concentration of the solubilized ECM solution by tallying up the volumes added to neutralize and the volumes removed to test the pH. Then add one times PBS to reach the desired final concentration here. Six milligrams per milliliter.On the day of surgery, prepare a 75 microliter injection of solubilized ECM in a 0.1 milliliter syringe tipped with a 30 gauge needle. Maintain anesthesia of an intubated female Harlan dolly rat with 2.5%ice of fluorine. Add eye, then verify anesthesia by performing a toe pinch.Administer three milliliters of lactated ringer solution by subcutaneous injection in the lower abdomen for hydration. Next, place the animal in a supine position on the surgical table and gently tape down the limbs. Use clippers to remove the hair on the abdomen and vacuum up the free hair.Make a series of 50 microliter injections of 2%lidocaine along a diagonal from the xiphoid process to the lower right hand side of the abdomen. Then scrub three times with Betadine starting in the middle and moving outward. Repeat the scrubbing with isop profile alcohol.Then cover the animal using a surgical drape with a pre-made circular window. Secure with a surgical drape. Using a number 10 scalpel.Make a three to four centimeter incision from the xiphoid process to the lower right hand side of the abdomen. Locate the xiphoid process and dissect vertically down through the muscle to the right, being careful to avoid the large vessel on the right. Next, use scissors to cut laterally through the muscle exposing the diaphragm.Be careful to avoid the liver using a 36 inch length of three zero Vicryl suture and a pair of hemostats. Drive one needle through the xiphoid process and pull the suture halfway through. Tape the ends of the suture together and fix them to a point above and behind the animal, lifting the xiphoid up and exposing the diaphragm with another 36 inch length of three zero Vicryl suture.Drive a needle through the muscle closest to the xiphoid process and again, pull through and fix the end to another point to the right of the surgical table, fully exposing the surgical cavity. Next, using a small pair of rat tooth micro forceps, grab the center of the diaphragm, pull it out, and make a very small incision with blunt scissors. Once this hole has been made, the lungs will retract.Make a two to three centimeter incision vertically through the diaphragm to visualize the heart. Then insert a three inch swab to the left of the cavity and push the lungs outta the way. Secure the swab in place using a towel clamp.Using another swab, move the right lung outta the way in order to locate the pericardial sack. Then using a pair of micro forceps and a pair of large serrated forceps, tear through the pericardial sack, exposing the apex of the heart. Grab the apex of the heart with the right tooth micro forceps and insert the needle to inject the solubilized matrix beveled edge to the left.A third of the way up from the apex parallel to the epicardial surface. Be sure to avoid the great cardiac vein. Inject the solubilized matrix gel and wait a couple of seconds before removing the needle.The tissue should whiten at the site of injection, swab away blood in the cavity, and remove the towel clamp and swab holding the right lung using curved micro hemostats, make an initial knot with a 30 inch length of five zero proline suture. Then use the rat tooth micro forceps to close the diaphragm with a continuous suture and a tapered needle before closing entirely. Insert PE one 60 suction tubing and close around using a 10 milliliter syringe to evacuate the chest cavity.As the suture is tightened, the diaphragm should be concave. Turn the ice of fluorine down to 1%Take out both three zero Vicryl sutures holding the cavity open. Hydrate the muscle wiping excess away with a swab or sterile gauze.Use a new length of three zero suture to close the muscle layer with intermittent sutures. Then turn the isof fluorine off. Clean the area and use staples to close the skin.Then apply a triple antibiotic ointment to the incision site. Allow the rat to recover under 100%oxygen. When the animal starts to breathe around the ventilator, remove the trachea tube.Once the animal is back on its feet, administer a subcutaneous injection of 0.05 milligrams per kilogram of buprenorphine hydrochloride analgesic, and return it to the home cage on a sterile towel. Cardiac tissue from rats injected with soluble matrix gels was sectioned and stained with hemat, toin, and eoin for gross tissue analysis at various time points. Following surgery at early time points, the injected region appears as a pink fibrous network that has spread interstitial at later time points.Cell influx is observed after two weeks. Degradation of the injected matrix is seen. If the ECM was labeled with biotin before injecting, it can be more directly visualized by staining the biotin with HRP conjugated streptavidin to visualize vessel ingrowth and formation in the matrix injection region.The slides here have been co stained with a fitzy. Conjugated is selectin that binds to endothelial cells shown in green, and an antis smooth muscle. Actin antibody shown in red stem cells may also be identified near the injection region.Here they have been visualized with an immunohistochemistry stain for C kit. After watching this video, you should have a good understanding how to create solubilized ECM from decellularized tissue and tested in vivo for cardiac tissue engineering applications. Don't forget that while we use pericardial tissue, this general procedure to be modified, to be used with any tissue source.Thank you for watching and good luck with your experiments.

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Research

JoVE Journal

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