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Method Article

Fabrication of Biologically Derived Injectable Materials for Myocardial Tissue Engineering

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DOI:

10.3791/2109

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December 20th, 2010

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In This Article

Summary

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

Abstract

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.

Protocol

1. Pre-processing Tissue Preparation

  1. 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).
  2. 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 over....

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Discussion

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.......

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Disclosures

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.

Acknowledgements

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.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Reagents:
PepsinSigma-Aldrichp6887-1GLyophilized
BiotinThermo Fisher Scientific, Inc.21217
Neutravidin-HRPThomas Scientific21130
Equipment:
Wiley Mini MillThomas Scientific3383L10
Labconco LyophilizerLabconco Corp.7670520
Surgical supplies:
BetadinePurdue Products L.P.67618-154-16
Lactated Ringers SolutionMWI Veterinary Supply003966
KY JellyMWI Veterinary Supply28658
Lidocaine, 2%MWI Veterinary Supply17767
Buprenorphine hydrochlorideReckitt Benckiser12496-0757-1
Artificial tear ointmentFisher ScientificNC9860843
Triple antibiotic ointmentFisher Scientific19082795
IsofluraneMWI Veterinary Supply60307-120-25
Otoscope MWI Veterinary Supply008699
Stop cockMWI Veterinary Supply006245
3-0 Vicrile sutureMWI Veterinary SupplyJ327H
5-0 Proline sutureMWI Veterinary Supplys-1173
Reverse cutting (RC) needleEthicon Inc.8684G
Microhemostats Fine Science Tools13013-14
Rat tooth microforcepsFine Science Tools11084-07
No. 10 scalpelFine Science Tools10110-01
Blunt scissorsFine Science Tools14108-09
Sharp, curved scissorsFine Science Tools14085-08
Large, serrated forcepsFine Science Tools1106-12
PE160 suction tubingBD Biosciences427430
Clippers MWI Veterinary Supply21608
Skin staples/stapler Ethicon Inc.PRR35
General supplies:
Stir plates
0.1 M HCl
1 M NaOH
10x PBS
1x PBS
70% Ethanol
0.1 mL syringes
10 mL syringe
Q-tips
Surgical glue
Surgical drape
Towel clamps
Small hand-held vacuum

References

  1. Seif-Naraghi, S. B., Salvatore, M. A., Magoffin-Schup, P. J., Hu, D. P., Christman, K. L. Design and characterization of an injectable pericardial matrix gel: A potentially autologous scaffold for cardiac tissue engineering. Tissue Engineering. , (2009).
  2. Freytes, D. O., Martin, J., Velankar, S. S., Lee, A. S., Badylak, S. F.

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