The use of acellular matrices for the tissue engineering of cardiac valves

被引:67
作者
Knight, R. L. [1 ]
Wilcox, H. E. [1 ]
Korossis, S. A. [1 ]
Fisher, J. [1 ]
Ingham, E. [1 ]
机构
[1] Univ Leeds, Fac Biol Sci, Inst Med & Biol Engn, Leeds LS2 9JT, W Yorkshire, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
tissue engineering; heart valve; xenogeneic;
D O I
10.1243/09544119JEIM230
中图分类号
R318 [生物医学工程];
学科分类号
0831 [生物医学工程];
摘要
Tissue-engineering approaches to cardiac valve replacement have made considerable advances over recent years and it is likely that this application will realize clinical success in the near future. Research in this area has been driven by the inadequacy of the currently available cardiac valve prostheses for younger patients who require multiple reoperations as they grow and develop. Tissue engineering has the potential to provide a valve capable of the same growth, repair, and regeneration as a natural valve and could improve outcomes for patients of all ages. Owing to the function and physical environment of the cardiac valve, the development of tissue-engineered replacements is unusual in that the biomechanical properties of the construct must dominate the biological properties in order for the valve to be functional at the time of implantation. As a result of this, conventional tissue-engineering scaffolds based on biodegradable polymers or collagen may not at present be suitable in this situation because of their initial limited strength. Research into the use of acellular xenogeneic and allogeneic matrices for tissue-engineered heart valves has consequently become extremely popular since the biomechanical properties of the valve can potentially be preserved with an optimal decellularization technique that removes the cells without damaging the matrix. A number of acellular scaffolds have already been tested clinically both unseeded and preseeded with cells and these have met with variable results. This article reviews the concepts involved and the advantages and disadvantages of the different approaches to tissue engineering a living cardiac valve.
引用
收藏
页码:129 / 143
页数:15
相关论文
共 102 条
[1]
[Anonymous], 2001, GUIDE PROPERTIES USE
[2]
Endothelial cells in culture: A model for studying vascular functions [J].
Bachetti, T ;
Morbidelli, L .
PHARMACOLOGICAL RESEARCH, 2000, 42 (01) :9-19
[3]
Tissue engineering of heart valves - human endothelial cell seeding of detergent acellularized porcine valves [J].
Bader, A ;
Schilling, T ;
Teebken, OE ;
Brandes, G ;
Herden, T ;
Steinhoff, G ;
Haverich, A .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 1998, 14 (03) :279-284
[4]
Mid-term findings on echocardiography and computed tomography after RVOT-reconstruction: comparison of decellularized (SynerGraft) and conventional allografts [J].
Bechtel, JFM ;
Gellissen, J ;
Erasmi, AW ;
Petersen, M ;
Hiob, A ;
Stierle, U ;
Sievers, HH .
EUROPEAN JOURNAL OF CARDIO-THORACIC SURGERY, 2005, 27 (03) :410-415
[5]
Bechtel JFM, 2003, J HEART VALVE DIS, V12, P734
[6]
DAMAGE OF PORCINE AORTIC-VALVE TISSUE CAUSED BY THE SURFACTANT SODIUMDODECYLSULFATE [J].
BODNAR, E ;
OLSEN, EGJ ;
FLORIO, R ;
DOBRIN, J .
THORACIC AND CARDIOVASCULAR SURGEON, 1986, 34 (02) :82-85
[7]
Booth C, 2002, J HEART VALVE DIS, V11, P457
[9]
Construction of autologous human heart valves based on an acellular allograft matrix [J].
Cebotari, S ;
Mertsching, H ;
Kallenbach, K ;
Kostin, S ;
Repin, O ;
Batrinac, A ;
Kleczka, C ;
Ciubotaru, A ;
Haverich, A .
CIRCULATION, 2002, 106 (13) :I63-I68
[10]
*CED SIN HLTH SYST, 2006, CED SIN MED CTR PROS