全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Myocardial Restoration: Is It the Cell or the Architecture or Both?

DOI: 10.1155/2012/240497

Full-Text   Cite this paper   Add to My Lib

Abstract:

Myocardial infarction is the leading cause of death in developed countries. Cardiac cell therapy has been introduced to clinical trials for more than ten years but its results are still controversial. Tissue engineering has addressed some limitations of cell therapy and appears to be a promising solution for cardiac regeneration. In this review, we would like to summarize the current understanding about the therapeutic effect of cell therapy and tissue engineering under purview of functional and structural aspects, highlighting actual roles of each therapy towards clinical application. 1. Introduction Ischemic heart disease is the principal cause of chronic heart failure in developed countries. In the USA alone, it causes 400,000 deaths annually [1]. The currently available therapies (i.e., pharmacological, interventional, and surgical methods) are unable to revitalize dead myocardium. Therefore, they cannot halt or reverse the development of congestive heart failure (CHF). Though cardiomyocytes in nonmammalian vertebrate species, like zebrafish, can restore the injured myocardium through proliferation and differentiation, this mechanism is not significant in humans [2]. Cardiac transplantation, the sole definitive therapy with long-term effect for end-stage HF so far, remains limited due to the scarcity of heart donors [3]. Myocardial restoration therapies, including cardiac cell therapy and cardiac tissue engineering, sound promising for a failing heart [4] as their ultimate goals are to regenerate the injured myocardium by robust and viable cells or artificial tissues. Although 10 years passed since Menasche et al. launched the first clinical trial [5], cardiac cell therapy has not become a well-established medical treatment for postmyocardial infarction (MI) patients. Delivery of cell suspensions to the myocardium is limited by various factors, such as insufficient cell retention and survival [6]. The introduction of cell-cell mechanical interaction systems, in the form of either cell sheets or biomaterial scaffolds [7] has addressed the issues related to poor cell retention and survival. Moreover, this strategy may offer a three-dimensional homogeneous cell delivery plus structural support (scaffold) to the myocardial area of ischemic injury [7]. Yet, there are no clinical studies of this approach. Though both cardiac cell therapy and tissue engineering have resulted in some improvement of function and structure of the injured heart, it would still be a laborious mission to reproduce the “real” myocardium. In this review, we would like to summarize

References

[1]  D. Lloyd-Jones, R. J. Adams, T. M. Brown et al., “Executive summary: heart disease and stroke statistics—2010 update: a report from the American Heart Association,” Circulation, vol. 121, no. 7, pp. e46–e215, 2010.
[2]  C. Jopling, E. Sleep, M. Raya, M. Martí, A. Raya, and J. C. I. Belmonte, “Zebrafish heart regeneration occurs by cardiomyocyte dedifferentiation and proliferation,” Nature, vol. 464, no. 7288, pp. 606–609, 2010.
[3]  B. A. Boilson, E. Raichlin, S. J. Park, and S. S. Kushwaha, “Device therapy and cardiac transplantation for end-stage heart failure,” Current Problems in Cardiology, vol. 35, no. 1, pp. 8–64, 2010.
[4]  W. H. Zimmermann, “Remuscularizing failing hearts with tissue engineered myocardium,” Antioxidants & Redox Signaling, vol. 11, no. 8, pp. 2011–2023, 2009.
[5]  P. Menasche, O. Alfieri, S. Janssens et al., “The Myoblast Autologous Grafting in Ischemic Cardiomyopathy (MAGIC) trial: first randomized placebo-controlled study of myoblast transplantation,” Circulation, vol. 117, no. 9, pp. 1189–1200, 2008.
[6]  Q. T. Bui, Z. M. Gertz, and R. L. Wilensky, “Intracoronary delivery of bone-marrow-derived stem cells,” Stem Cell Research & Therapy, vol. 1, no. 4, p. 29, 2010.
[7]  J. Leor, Y. Amsalem, and S. Cohen, “Cells, scaffolds, and molecules for myocardial tissue engineering,” Pharmacology & Therapeutics, vol. 105, no. 2, pp. 151–163, 2005.
[8]  T. Kofidis, “Alternative cardiac therapies: stem cells and tissue engineering for the heart,” CTSNet, 2006.
[9]  G. D. Buckberg, “Basic science review: the helix and the heart,” The Journal of Thoracic and Cardiovascular Surgery, vol. 124, no. 5, pp. 863–883, 2002.
[10]  W. B. R. Mill, M. R. Anderson, and R. Hi, “Surgical anatomy of the heart,” in Surgery in the Adult, L. Cohn, Ed., pp. 29–50, McGraw-Hill, New York, NY, USA, 3 edition, 2008.
[11]  G. Ertl, P. Gaudran, S. Neubauer et al., “Cardiac dysfunction and development of heart failure,” European Heart Journal, vol. 14, supplement A, pp. 33–37, 1993.
[12]  J. N. Cohn, R. Ferrari, and N. Sharpe, “Cardiac remodeling—concepts and clinical implications: a consensus paper from an international forum on cardiac remodeling,” Journal of the American College of Cardiology, vol. 35, no. 3, pp. 569–582, 2000.
[13]  J. E. Udelson and M. A. Konstam, “Relation between left ventricular remodeling and clinical outcomes in heart failure patients with left ventricular systolic dysfunction,” Journal of Cardiac Failure, vol. 8, no. 6, supplement, pp. S465–S471, 2002.
[14]  E. Martin-Rendon, S. J. Brunskill, C. J. Hyde, S. J. Stanworth, A. Mathur, and S. M. Watt, “Autologous bone marrow stem cells to treat acute myocardial infarction: a systematic review,” European Heart Journal, vol. 29, no. 15, pp. 1807–1818, 2008.
[15]  B. Assmus, A. Rolf, S. Erbs et al., “Clinical outcome 2 years after intracoronary administration of bone marrow-derived progenitor cells in acute myocardial infarction,” Circulation: Heart Failure, vol. 3, no. 1, pp. 89–96, 2010.
[16]  A. M. van der Laan, A. Hirsch, R. Nijveldt et al., “Bone marrow cell therapy after acute myocardial infarction: the HEBE trial in perspective, first results,” Netherlands Heart Journal, vol. 16, no. 12, pp. 436–439, 2008.
[17]  S. Mansour, M. Vanderheyden, B. De Bruyne et al., “Intracoronary delivery of hematopoietic bone marrow stem cells and luminal loss of the infarct-related artery in patients with recent myocardial infarction,” Journal of the American College of Cardiology, vol. 47, no. 8, pp. 1727–1730, 2006.
[18]  C. Steinwender, R. Hofmann, A. Kypta et al., “In-stent restenosis in bare metal stents versus sirolimus-eluting stents after primary coronary intervention for acute myocardial infarction and subsequent transcoronary transplantation of autologous stem cells,” Clinical Cardiology, vol. 31, no. 8, pp. 356–359, 2008.
[19]  D. A. Taylor, B. Z. Atkins, P. Hungspreugs et al., “Regenerating functional myocardium: improved performance after skeletal myoblast transplantation,” Nature Medicine, vol. 4, no. 8, pp. 929–933, 1998.
[20]  J. Herrerosa, F. Prósper, A. Perez et al., “Autologous intramyocardial injection of cultured skeletal muscle-derived stem cells in patients with non-acute myocardial infarction,” European Heart Journal, vol. 24, no. 22, pp. 2012–2020, 2003.
[21]  M. R. Abraham, C. A. Henrikson, L. Tung et al., “Antiarrhythmic engineering of skeletal myoblasts for cardiac transplantation,” Circulation Research, vol. 97, no. 2, pp. 159–167, 2005.
[22]  J. Leor, M. Patterson, M. J. Quinones, L. H. Kedes, and R. A. Kloner, “Transplantation of fetal myocardial tissue into the infarcted myocardium of rat: a potential method for repair of infarcted myocardium?” Circulation, vol. 94, no. 9, supplement, pp. II332–II336, 1996.
[23]  K. B. S. Pasumarthi and L. J. Field, “Cardiomyocyte cell cycle regulation,” Circulation Research, vol. 90, no. 10, pp. 1044–1054, 2002.
[24]  V. Di Stefano, M. Giacca, M. C. Capogrossi, M. Crescenzi, and F. Martelli, “Knockdown of cyclin-dependent kinase inhibitors induces cardiomyocyte re-entry in the cell cycle,” The Journal of Biological Chemistry, vol. 286, no. 10, pp. 8644–8654, 2011.
[25]  A. P. Beltrami, K. Urbanek, J. Kajstura et al., “Evidence that human cardiac myocytes divide after myocardial infarction,” The New England Journal of Medicine, vol. 344, no. 23, pp. 1750–1757, 2001.
[26]  X. L. Tang, G. Rokosh, S. K. Sanganalmath et al., “Intracoronary administration of cardiac progenitor cells alleviates left ventricular dysfunction in rats with a 30-day-old infarction,” Circulation, vol. 121, no. 2, pp. 293–305, 2010.
[27]  H. Maxeiner, N. Krehbiehl, A. Müller et al., “New insights into paracrine mechanisms of human cardiac progenitor cells,” European Journal of Heart Failure, vol. 12, no. 7, pp. 730–737, 2010.
[28]  K. R. Boheler, J. Czyz, D. Tweedie, H. T. Yang, S. V. Anisimov, and A. M. Wobus, “Differentiation of pluripotent embryonic stem cells into cardiomyocytes,” Circulation Research, vol. 91, no. 3, pp. 189–201, 2002.
[29]  O. Caspi, I. Huber, I. Kehat et al., “Transplantation of human embryonic stem cell-derived cardiomyocytes improves myocardial performance in infarcted rat hearts,” Journal of the American College of Cardiology, vol. 50, no. 19, pp. 1884–1893, 2007.
[30]  G. Blin, D. Nury, S. Stefanovic et al., “A purified population of multipotent cardiovascular progenitors derived from primate pluripotent stem cells engrafts in postmyocardial infarcted nonhuman primates,” Journal of Clinical Investigation, vol. 120, no. 4, pp. 1125–1139, 2010.
[31]  H. Vidarsson, J. Hyllner, and P. Sartipy, “Differentiation of human embryonic stem cells to cardiomyocytes for in vitro and in vivo applications,” Stem Cell Reviews and Reports, vol. 6, no. 1, pp. 108–120, 2010.
[32]  M. Kucia, R. Reca, F. R. Campbell et al., “A population of very small embryonic-like (VSEL) CXCR4+ SSEA-1+Oct-4+ stem cells identified in adult bone marrow,” Leukemia, vol. 20, no. 5, pp. 857–869, 2006.
[33]  E. K. Zuba-Surma, Y. Guo, H. Taher et al., “Transplantation of expanded bone marrow-derived very small embryonic-like stem cells (VSEL-SCs) improves left ventricular function and remodelling after myocardial infarction,” Journal of Cellular and Molecular Medicine, vol. 15, no. 6, pp. 1319–1328, 2011.
[34]  K. Takahashi and S. Yamanaka, “Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors,” Cell, vol. 126, no. 4, pp. 663–676, 2006.
[35]  D. Orlic, J. Kajstura, S. Chimenti et al., “Bone marrow cells regenerate infarcted myocardium,” Nature, vol. 410, no. 6829, pp. 701–705, 2001.
[36]  Y. Miyahara, N. Nagaya, M. Kataoka et al., “Monolayered mesenchymal stem cells repair scarred myocardium after myocardial infarction,” Nature Medicine, vol. 12, no. 4, pp. 459–465, 2006.
[37]  L. B. Balsam, A. J. Wagers, J. L. Christensen, T. Kofidis, I. L. Weissmann, and R. C. Robbins, “Haematopoietic stem cells adopt mature haematopoietic fates in ischaemic myocardium,” Nature, vol. 428, no. 6983, pp. 668–673, 2004.
[38]  A. Abdel-Latif, R. Bolli, I. M. Tleyjeh et al., “Adult bone marrow-derived cells for cardiac repair: a systematic review and meta-analysis,” Archives of Internal Medicine, vol. 167, no. 10, pp. 989–997, 2007.
[39]  A. P. Beltrami, L. Barlucchi, D. Torella et al., “Adult cardiac stem cells are multipotent and support myocardial regeneration,” Cell, vol. 114, no. 6, pp. 763–776, 2003.
[40]  A. I. Caplan and J. E. Dennis, “Mesenchymal stem cells as trophic mediators,” Journal of Cellular Biochemistry, vol. 98, no. 5, pp. 1076–1084, 2006.
[41]  M. Jain, H. DerSimonian, D. A. Brenner et al., “Cell therapy attenuates deleterious ventricular remodeling and improves cardiac performance after myocardial infarction,” Circulation, vol. 103, no. 14, pp. 1920–1927, 2001.
[42]  S. Ghostine, C. Carrion, L. C. G. Souza et al., “Long-term efficacy of myoblast transplantation on regional structure and function after myocardial infarction,” Circulation, vol. 106, no. 12, supplement 1, pp. I131–I136, 2002.
[43]  Y. Sawa, “Myocardial regeneration for heart failure,” Nippon Rinsho, vol. 68, no. 4, pp. 719–725, 2010.
[44]  M. A. Laflamme, S. Zbinden, S. E. Epstein, and C. E. Murry, “Cell-based therapy for myocardial ischemia and infarction: pathophysiological mechanisms,” Annual Review of Pathology, vol. 2, pp. 307–339, 2007.
[45]  V. F. M. Segers and R. T. Lee, “Stem-cell therapy for cardiac disease,” Nature, vol. 451, no. 7181, pp. 937–942, 2008.
[46]  M. Mathieu, J. Bartunek, B. El Oumeiri et al., “Cell therapy with autologous bone marrow mononuclear stem cells is associated with superior cardiac recovery compared with use of nonmodified mesenchymal stem cells in a canine model of chronic myocardial infarction,” The Journal of Thoracic and Cardiovascular Surgery, vol. 138, no. 3, pp. 646–653, 2009.
[47]  J. Makela, K. Ylitalo, S. Lehtonen et al., “Bone marrow-derived mononuclear cell transplantation improves myocardial recovery by enhancing cellular recruitment and differentiation at the infarction site,” The Journal of Thoracic and Cardiovascular Surgery, vol. 134, no. 3, pp. 565–573, 2007.
[48]  E. C. Perin, G. V. Silva, T. D. Henry et al., “A randomized study of transendocardial injection of autologous bone marrow mononuclear cells and cell function analysis in ischemic heart failure (FOCUS-HF),” American Heart Journal, vol. 161, no. 6, pp. 1078–1087, 2011.
[49]  J. Feygin, A. Mansoor, P. Eckman, C. Swingen, and J. Zhang, “Functional and bioenergetic modulations in the infarct border zone following autologous mesenchymal stem cell transplantation,” American Journal of Physiology, vol. 293, no. 3, pp. H1772–H1780, 2007.
[50]  Y. Amsalem, Y. Mardor, M. S. Feinberg et al., “Iron-oxide labeling and outcome of transplanted mesenchymal stem cells in the infarcted myocardium,” Circulation, vol. 116, no. 11, supplement, pp. I38–I45, 2007.
[51]  S. L. Chen, W. W. Fang, J. Qian et al., “Improvement of cardiac function after transplantation of autologous bone marrow mesenchymal stem cells in patients with acute myocardial infarction,” Chinese Medical Journal, vol. 117, no. 10, pp. 1443–1448, 2004.
[52]  B. Dawn, S. Tiwari, M. J. Kucia et al., “Transplantation of bone marrow-derived very small embryonic-like stem cells attenuates left ventricular dysfunction and remodeling after myocardial infarction,” Stem Cells, vol. 26, no. 6, pp. 1646–1655, 2008.
[53]  C. Mauritz, A. Martens, S. V. Rojas, et al., “Induced pluripotent stem cell (iPSC)-derived Flk-1 progenitor cells engraft, differentiate, and improve heart function in a mouse model of acute myocardial infarction,” European Heart Journal, vol. 32, no. 21, pp. 2634–2641, 2011.
[54]  H. Q. Ly, K. Hoshino, I. Pomerantseva et al., “In vivo myocardial distribution of multipotent progenitor cells following intracoronary delivery in a swine model of myocardial infarction,” European Heart Journal, vol. 30, no. 23, pp. 2861–2868, 2009.
[55]  A. Aicher, W. Brenner, M. Zuhayra et al., “Assessment of the tissue distribution of transplanted human endothelial progenitor cells by radioactive labeling,” Circulation, vol. 107, no. 16, pp. 2134–2139, 2003.
[56]  M. Hofmann, K. C. Wollert, G. P. Meyer et al., “Monitoring of bone marrow cell homing into the infarcted human myocardium,” Circulation, vol. 111, no. 17, pp. 2198–2202, 2005.
[57]  K. Cheng, T. S. Li, K. Malliaras, D. R. Davis, Y. Zhang, and E. Marbán, “Magnetic targeting enhances engraftment and functional benefit of iron-labeled cardiosphere-derived cells in myocardial infarction,” Circulation Research, vol. 106, no. 10, pp. 1570–1581, 2010.
[58]  M. Zhang, D. Methot, V. Poppa, Y. Fujio, K. Walsh, and C. E. Murry, “Cardiomyocyte grafting for cardiac repair: graft cell death and anti-death strategies,” Journal of Molecular and Cellular Cardiology, vol. 33, no. 5, pp. 907–921, 2001.
[59]  T. E. Robey, M. K. Saiget, H. Reinecke, and C. E. Murry, “Systems approaches to preventing transplanted cell death in cardiac repair,” Journal of Molecular and Cellular Cardiology, vol. 45, no. 4, pp. 567–581, 2008.
[60]  J. W?hrle, N. Merkle, V. Mail?nder et al., “Results of intracoronary stem cell therapy after acute myocardial infarction,” The American Journal of Cardiology, vol. 105, no. 6, pp. 804–812, 2010.
[61]  R. Gaetani, L. Barile, E. Forte et al., “New perspectives to repair a broken heart,” Cardiovascular & Hematological Agents in Medicinal Chemistry, vol. 7, no. 2, pp. 91–107, 2009.
[62]  A. Kawamoto, H. Iwasaki, K. Kusano et al., “CD34-positive cells exhibit increased potency and safety for therapeutic neovascularization after myocardial infarction compared with total mononuclear cells,” Circulation, vol. 114, no. 20, pp. 2163–2169, 2006.
[63]  H. M. Klein, A. Ghodsizad, R. Marktanner et al., “Intramyocardial implantation of CD133+ stem cells improved cardiac function without bypass surgery,” The Heart Surgery Forum, vol. 10, no. 1, pp. E66–E69, 2007.
[64]  D. S. Adler, H. Lazarus, R. Nair et al., “Safety and efficacy of bone marrow-derived autologous CD133+ stem cell therapy,” Frontiers in Bioscience, vol. 3, pp. 506–514, 2011.
[65]  Y. Wang, H. K. Haider, N. Ahmad, M. Xu, R. Ge, and M. Ashraf, “Combining pharmacological mobilization with intramyocardial delivery ofbone marrow cells over-expressing VEGF is more effective forcardiac repair,” Journal of Molecular and Cellular Cardiology, vol. 40, no. 5, pp. 736–745, 2006.
[66]  M. Gnecchi, H. He, N. Noiseux et al., “Evidence supporting paracrine hypothesis for Akt-modified mesenchymal stem cell-mediated cardiac protection and functional improvement,” The FASEB Journal, vol. 20, no. 6, pp. 661–669, 2006.
[67]  B. Krausgrill, M. Vantler, V. Burst et al., “Influence of cell treatment with PDGF-BB and reperfusion on cardiac persistence of mononuclear and mesenchymal bone marrow cells after transplantation into acute myocardial infarction in rats,” Cell Transplantation, vol. 18, no. 8, pp. 847–853, 2009.
[68]  S. Fernandes, A. V. Naumova, W. Z. Zhu, M. A. Laflamme, J. Gold, and C. E. Murry, “Human embryonic stem cell-derived cardiomyocytes engraft but do not alter cardiac remodeling after chronic infarction in rats,” Journal of Molecular and Cellular Cardiology, vol. 49, no. 6, pp. 941–949, 2010.
[69]  J. Meluzin, J. Mayer, L. Groch et al., “Autologous transplantation of mononuclear bone marrow cells in patients with acute myocardial infarction: the effect of the dose of transplanted cells on myocardial function,” American Heart Journal, vol. 152, no. 5, pp. 975.e9–975.e15, 2006.
[70]  R. Gaetani, G. Rizzitelli, I. Chimenti et al., “Cardiospheres and tissue engineering for myocardial regeneration: potential for clinical application,” Journal of Cellular and Molecular Medicine, vol. 14, no. 5, pp. 1071–1077, 2010.
[71]  J. Leor, S. Aboulafia-Etzion, A. Dar et al., “Bioengineered cardiac grafts: a new approach to repair the infarcted myocardium?” Circulation, vol. 102, no. 19, supplement 3, pp. III56–III61, 2000.
[72]  W. H. Zimmermann, K. Schneiderbanger, P. Schubert et al., “Tissue engineering of a differentiated cardiac muscle construct,” Circulation Research, vol. 90, no. 2, pp. 223–230, 2002.
[73]  W. H. Zimmermann, I. Melnychenko, G. Wasmeier et al., “Engineered heart tissue grafts improve systolic and diastolic function in infarcted rat hearts,” Nature Medicine, vol. 12, no. 4, pp. 452–458, 2006.
[74]  T. Shimizu, M. Yamato, A. Kikuchi, and T. Okano, “Cell sheet engineering for myocardial tissue reconstruction,” Biomaterials, vol. 24, no. 13, pp. 2309–2316, 2003.
[75]  T. Shimizu, H. Sekine, M. Yamato, and T. Okano, “Cell sheet-based myocardial tissue engineering: new hope for damaged heart rescue,” Current Pharmaceutical Design, vol. 15, no. 24, pp. 2807–2814, 2009.
[76]  T. Shimizu, H. Sekine, Y. Isoi, M. Yamato, A. Kikuchi, and T. Okano, “Long-term survival and growth of pulsatile myocardial tissue grafts engineered by the layering of cardiomyocyte sheets,” Tissue Engineering, vol. 12, no. 3, pp. 499–507, 2006.
[77]  T. Ozawa, D. A. G. Mickle, R. D. Weisel et al., “Histologic changes of nonbiodegradable and biodegradable biomaterials used to repair right ventricular heart defects in rats,” The Journal of Thoracic and Cardiovascular Surgery, vol. 124, no. 6, pp. 1157–1164, 2002.
[78]  K. A. Robinson, J. Li, M. Mathison et al., “Extracellular matrix scaffold for cardiac repair,” Circulation, vol. 112, no. 9, supplement, pp. I135–I143, 2005.
[79]  T. Kofidis, D. R. Lebl, E. C. Martinez, G. Hoyt, M. Tanaka, and R. C. Robbins, “Novel injectable bioartificial tissue facilitates targeted, less invasive, large-scale tissue restoration on the beating heart after myocardial injury,” Circulation, vol. 112, no. 9, supplement, pp. I173–I177, 2005.
[80]  J. M. Singelyn, J. A. DeQuach, S. B. Seif-Naraghi, R. B. Littlefield, P. J. Schup-Magoffin, and K. L. Christman, “Naturally derived myocardial matrix as an injectable scaffold for cardiac tissue engineering,” Biomaterials, vol. 30, no. 29, pp. 5409–5416, 2009.
[81]  J. M. Singelyn and K. L. Christman, “Modulation of material properties of a decellularized myocardial matrix scaffold,” Journal of Macromolecular Bioscience, vol. 11, no. 6, pp. 731–738, 2011.
[82]  Y. Miyagi, F. Zeng, X. P. Huang et al., “Surgical ventricular restoration with a cell- and cytokine-seeded biodegradable scaffold,” Biomaterials, vol. 31, no. 30, pp. 7684–7694, 2010.
[83]  H. C. Ott, T. S. Matthiesen, S. K. Goh et al., “Perfusion-decellularized matrix: using nature's platform to engineer a bioartificial heart,” Nature Medicine, vol. 14, no. 2, pp. 213–221, 2008.
[84]  A. N. Morritt, S. K. Bortolotto, R. J. Dilley et al., “Cardiac tissue engineering in an in vivo vascularized chamber,” Circulation, vol. 115, no. 3, pp. 353–360, 2007.
[85]  M. Radisic, H. Park, T. P. Martens et al., “Pre-treatment of synthetic elastomeric scaffolds by cardiac fibroblasts improves engineered heart tissue,” Journal of Biomedical Materials Research A, vol. 86, no. 3, pp. 713–724, 2008.
[86]  R. K. Iyer, L. L. Y. Chiu, and M. Radisic, “Microfabricated poly(ethylene glycol) templates enable rapid screening of triculture conditions for cardiac tissue engineering,” Journal of Biomedical Materials Research A, vol. 89, no. 3, pp. 616–631, 2009.
[87]  E. C. Martinez, J. Wang, S. U. Gan, R. Singh, C. N. Lee, and T. Kofidis, “Ascorbic acid improves embryonic cardiomyoblast cell survival and promotes vascularization in potential myocardial grafts in vivo,” Tissue Engineering A, vol. 16, no. 4, pp. 1349–1361, 2010.
[88]  T. Sasagawa, T. Shimizu, S. Sekiya et al., “Design of prevascularized three-dimensional cell-dense tissues using a cell sheet stacking manipulation technology,” Biomaterials, vol. 31, no. 7, pp. 1646–1654, 2010.
[89]  T. Dvir, A. Kedem, E. Ruvinov et al., “Prevascularization of cardiac patch on the omentum improves its therapeutic outcome,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 35, pp. 14990–14995, 2009.
[90]  R. Suzuki, F. Hattori, Y. Itabashi et al., “Omentopexy enhances graft function in myocardial cell sheet transplantation,” Biochemical and Biophysical Research Communications, vol. 387, no. 2, pp. 353–359, 2009.
[91]  T. Kofidis, A. Lenz, J. Boublik et al., “Pulsatile perfusion and cardiomyocyte viability in a solid three-dimensional matrix,” Biomaterials, vol. 24, no. 27, pp. 5009–5014, 2003.
[92]  J. R. Frederick, J. R. Fitzpatrick III, R. C. McCormick et al., “Stromal cell-derived factor-1α activation of tissue-engineered endothelial progenitor cell matrix enhances ventricular function after myocardial infarction by inducing neovasculogenesis,” Circulation, vol. 122, no. 11, supplement, pp. S107–S117, 2010.
[93]  S. Miyagawa, A. Saito, T. Sakaguchi et al., “Impaired myocardium regeneration with skeletal cell sheets—a preclinical trial for tissue-engineered regeneration therapy,” Transplantation, vol. 90, no. 4, pp. 364–372, 2010.
[94]  J. C. Chachques, J. C. Trainini, N. Lago, M. Cortes-Morichetti, O. Schussler, and A. Carpentier, “Myocardial Assistance by Grafting a New Bioartificial Upgraded Myocardium (MAGNUM trial): clinical feasibility study,” Annals of Thoracic Surgery, vol. 85, no. 3, pp. 901–908, 2008.
[95]  U. Sartipy, A. Alb?ge, and D. Lindblom, “The Dor procedure for left ventricular reconstruction. Ten-year clinical experience,” European Journal of Cardio-Thoracic Surgery, vol. 27, no. 6, pp. 1005–1010, 2005.
[96]  P. Ferrazzi, M. Triggiani, A. Iacovoni et al., “Surgical ventricular restoration by means of a new technique to preserve left ventricular compliance: the horseshoe repair,” The Journal of Thoracic and Cardiovascular Surgery, vol. 136, no. 5, pp. 1382–1383, 2008.

Full-Text

comments powered by Disqus

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133