Thick acellular heart extracellular matrix with inherent vasculature: A potential platform for myocardial tissue regeneration

Tissue Engineering - Part A

Volumn 18, Issue 19-20, 2012, Pages 2125-2137

  Sarig, Udi ^a   Au Yeung, Gigi C T ^b   Wang, Yao ^b   Bronshtein, Tomer ^b   Dahan, Nitsan ^a   Boey, Freddy Y C ^b   Venkatraman, Subbu S ^b   MacHluf, Marcelle ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b NANYANG TECHNOLOGICAL UNIVERSITY   (Singapore)

Author keywords

[No Author keywords available]

Indexed keywords

BIOMECHANICS; CELLS; CYTOLOGY; ENERGY DISSIPATION; HEART; MASS SPECTROMETRY; MECHANICAL TESTING; PROTEINS; SODIUM; TISSUE; TOUGHNESS;

CARDIAC TISSUES; CELL REMOVAL; CELLULAR PROTEINS; CORONARY VESSEL; DECELLULARIZATION; DIFFUSION LIMITATIONS; ECM PROTEINS; EX-VIVO; EXTRACELLULAR MATRICES; FIBER MORPHOLOGY; HEART TISSUES; MASS SPECTROSCOPY; MYOCARDIAL TISSUE; MYOCARDIAL TISSUE ENGINEERING; PROGENITOR CELL; REGENERATION CAPACITY; SODIUM DODECYL SULFATE; STRESS-STRAIN; STRUCTURAL CHARACTERISTICS; SUCCESSFUL ISOLATION; TISSUE CONSTRUCTS; TISSUE SLAB; ULTIMATE STRESS; VASCULAR NETWORK; VASCULATURE;

SCAFFOLDS (BIOLOGY);

SUS;

TISSUE SCAFFOLD;

ANIMAL; ARTICLE; CELL ADHESION; CELL CULTURE; CHEMISTRY; CYTOLOGY; EXTRACELLULAR MATRIX; FEMALE; HEART MUSCLE; HUMAN; METABOLISM; METHODOLOGY; PHYSIOLOGY; RAT; SCANNING ELECTRON MICROSCOPY; SWINE; TISSUE ENGINEERING; UMBILICAL VEIN ENDOTHELIAL CELL;

ANIMALS; CELL ADHESION; CELLS, CULTURED; EXTRACELLULAR MATRIX; FEMALE; HUMAN UMBILICAL VEIN ENDOTHELIAL CELLS; HUMANS; MICROSCOPY, ELECTRON, SCANNING; MYOCARDIUM; RATS; SWINE; TISSUE ENGINEERING; TISSUE SCAFFOLDS;

EID: 84867007214     PISSN: 19373341     EISSN: 1937335X     Source Type: Journal    
DOI: 10.1089/ten.tea.2011.0586     Document Type: Article

References (36)

1. Sarig, U., and Machluf, M. Engineering cell platforms for myocardial regeneration. Expert Opin Biol Ther 11, 1055, 2011.
2. Schaaf, S., Shibamiya, A., Mewe, M., Eder, A., Stohr, A., Hirt, M.N., et al. Human engineered heart tissue as a versatile tool in basic research and preclinical toxicology. PloS One 6, e26397, 2011.
3. Zimmermann, W.H., Melnychenko, I., Wasmeier, G., Didie, M., Naito, H., Nixdorff, U., et al. Engineered heart tissue grafts improve systolic and diastolic function in infarcted rat hearts. Nat Med 12, 452, 2006.
4. Sawa, Y., Miyagawa, S., Sakaguchi, T., Fujita, T., Matsuyama, A., Saito, A., et al. Tissue engineered myoblast sheets improved cardiac function sufficiently to discontinue LVAS in a patient with DCM: report of a case. Surg Today 42, 181, 2012.
5. Kochupura, P.V., Azeloglu, E.U., Kelly, D.J., Doronin, S.V., Badylak, S.F., Krukenkamp, I.B., et al. Tissue-engineered myocardial patch derived from extracellular matrix provides regional mechanical function. Circulation 112, I144, 2005.
6. Robinson, K.A., Li, J., Mathison, M., Redkar, A., Cui, J., Chronos, N.A., et al. Extracellular matrix scaffold for cardiac repair. Circulation 112, I135, 2005.
7. Ott, H.C., Matthiesen, T.S., Goh, S.K., Black, L.D., Kren, S.M., Netoff, T.I., et al. Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart. Nat Med 14, 213, 2008.
8. Singelyn, J.M., DeQuach, J.A., Seif-Naraghi, S.B., Littlefield, R.B., Schup-Magoffin, P.J., and Christman, K.L. Naturally derived myocardial matrix as an injectable scaffold for cardiac tissue engineering. Biomaterials 30, 5409, 2009.
9. Eitan, Y., Sarig, U., Dahan, N., and Machluf, M. Acellular cardiac extracellular matrix as a scaffold for tissue engineering: in vitro cell support, remodeling, and biocompati-bility. Tissue Eng Part C Methods 16, 671, 2010.
10. Wainwright, J.M., Czajka, C.A., Patel, U.B., Freytes, D.O., Tobita, K., Gilbert, T.W., et al. Preparation of cardiac extracellular matrix from an intact porcine heart. Tissue Eng Part C Methods 16, 525, 2010.
11. Wang, B., Borazjani, A., Tahai, M., Curry, A.L., Simionescu, D.T., Guan, J., et al. Fabrication of cardiac patch with de-cellularized porcine myocardial scaffold and bone marrow mononuclear cells. J Biomed Mater Res A 94, 1100, 2010.
12. Akhyari, P., Aubin, H., Gwanmesia, P., Barth, M., Hoffmann, S., Huelsmann, J., et al. The quest for an optimized protocol for whole heart decellularization: a comparison of three popular and a novel decellularization technique and their diverse effects on crucial extracellular matrix qualities. Tissue Eng Part C Methods 17, 915, 2011.
13. Weymann, A., Loganathan, S., Takahashi, H., Schies, C., Claus, B., Hirschberg, K., et al. Development and evaluation of a perfusion decellularization porcine heart model\- generation of 3-dimensional myocardial neoscaffolds. Circ J 75, 852, 2011.
14. Christman, K.L., and Lee, R.J. Biomaterials for the treatment of myocardial infarction. J Am Coll Cardiol 48, 907, 2006.
15. Badylak, S.F., Taylor, D., and Uygun, K. Whole-organ tissue engineering: decellularization and recellularization of three-dimensional matrix scaffolds. Annu Rev Biomed Eng 13, 27, 2011.
16. Kaully, T., Kaufman-Francis, K., Lesman, A., and Levenberg, S. Vascularization\-the conduit to viable engineered tissues. Tissue Eng Part B Rev 15, 159, 2009.
17. Caspi, O., Lesman, A., Basevitch, Y., Gepstein, A., Arbel, G., Habib, I.H., et al. Tissue engineering of vascularized cardiac muscle from human embryonic stem cells. Circ Res 100, 263, 2007.
18. Shimizu, T., Sekine, H., Yang, J., Isoi, Y., Yamato, M., Ki-kuchi, A., et al. Polysurgery of cell sheet grafts overcomes diffusion limits to produce thick, vascularized myocardial tissues. FASEB J 20, 708, 2006.
19. Sekine, H., Shimizu, T., Hobo, K., Sekiya, S., Yang, J., Yamato, M., et al. Endothelial cell coculture within tissue-engineered cardiomyocyte sheets enhances neovasculariza-tion and improves cardiac function of ischemic hearts. Circulation 118, S145, 2008.
20. Tee, R., Lokmic, Z., Morrison, W.A., and Dilley, R.J. Strategies in cardiac tissue engineering. ANZ J Surg 80, 683, 2010.
21. Morritt, A.N., Bortolotto, S.K., Dilley, R.J., Han, X., Kompa, A.R., McCombe, D., et al. Cardiac tissue engineering in an in vivo vascularized chamber. Circulation 115, 353, 2007.
22. Chen, A.C., McNeilly, C., Liu, A.P., Flaim, C.J., Cuttle, L., Kendall, M., et al. Second harmonic generation and multiphoton microscopic detection of collagen without the need for species specific antibodies. Burns 37, 1001, 2011.
23. Lennon, D.P., and Caplan, A.I. Isolation of rat marrow-derived mesenchymal stem cells. Exp Hematol 34, 1606, 2006.
24. Varshavsky, A., Kessler, O., Abramovitch, S., Kigel, B., Zaffryar, S., Akiri, G., et al. Semaphorin-3B is an angiogen-esis inhibitor that is inactivated by furin-like pro-protein convertases. Cancer Res 68, 6922, 2008.
25. Crapo, P.M., Gilbert, T.W., and Badylak, S.F. An overview of tissue and whole organ decellularization processes. Biomaterials 32, 3233, 2011.
26. Brown, B.N., Freund, J.M., Han, L., Rubin, J.P., Reing, J.E., Jeffries, E.M., et al. Comparison of three methods for the derivation of a biologic scaffold composed of adipose tissue extracellular matrix. Tissue Eng Part C Methods 17, 411, 2010.
27. Graham, H.K., Horn, M., and Trafford, A.W. Extracellular matrix profiles in the progression to heart failure. European Young Physiologists Symposium Keynote Lecture-Bratislava 2007. Acta Physiol (Oxf) 194, 3, 2008.
28. Human protein databas (HPRD), Collagen, type II, alpha 1-site of expression, John hopkins university. Available at www.hprd.org/summary?hprd-id= 00361&isoform-id=003 61-1&isoform-name=Isoform-1. (retrived at: 4/7/2011).
29. Superti-Furga, A., Rocchi, M., Schafer, B.W., and Gitzel-mann, R. Complementary DNA sequence and chromosomal mapping of a human proteoglycan-binding cell-adhesion protein (dermatopontin). Genomics 17, 463, 1993.
30. Takemoto, S., Murakami, T., Kusachi, S., Iwabu, A., Hirohata, S., Nakamura, K., et al. Increased expression of dermato-pontin mRNA in the infarct zone of experimentally induced myocardial infarction in rats: comparison with decorin and type I collagen mRNAs. Basic Res Cardiol 97, 461, 2002.
31. Forbes, E.G., Cronshaw, A.D., MacBeath, J.R., and Hulmes, D.J. Tyrosine-rich acidic matrix protein (TRAMP) is a tyrosine-sulphated and widely distributed protein of the extracellular matrix. FEBS Lett 351, 433, 1994.
32. Okamoto, O., Fujiwara, S., Abe, M., and Sato, Y. Dermato-pontin interacts with transforming growth factor beta and enhances its biological activity. Biochem J 337, 537, 1999.
33. Stratman, A.N., Malotte, K.M., Mahan, R.D., Davis, M.J., and Davis, G.E. Pericyte recruitment during vasculogenic tube assembly stimulates endothelial basement membrane matrix formation. Blood 114, 5091, 2009.
34. Dalen, H., Thorstensen, A., Aase, S.A., Ingul, C.B., Torp, H., Vatten, L.J., et al. Segmental and global longitudinal strain and strain rate based on echocardiography of 1266 healthy individuals: the HUNT study in Norway. Eur J Echocardiogr 11, 176, 2010.
35. Badylak, S.F., and Gilbert, T.W. Immune response to biologic scaffold materials. Semin Immunol 20, 109, 2008.
36. Gilbert, T.W., Sellaro, T.L., and Badylak, S.F. Decellulariza-tion of tissues and organs. Biomaterials 27, 3675, 2006.