The in vitro development of autologous fibrin-based tissue-engineered heart valves through optimised dynamic conditioning

被引:107
作者
Flanagan, Thomas C.
Cornelissen, Christian
Koch, Sabine
Tschoeke, Beate
Sachweh, Joerg S.
Schmitz-Rode, Thomas
Jockenhoevel, Stefan
机构
[1] Univ Aachen, Rhein Westfal TH Aachen, Helmholtz Inst Biomed Engn, Cardiovasc tissue Engn Grp, D-52074 Aachen, Germany
[2] Univ Hosp, Dept Paediat Cardiac Surg, D-52074 Aachen, Germany
关键词
cardiovascular tissue engineering; heart valve; extracellular matrix; fibrin; bioreactor; immunochemistry;
D O I
10.1016/j.biomaterials.2007.04.012
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Our group has previously demonstrated the synthesis of a completely autologous fibrin-based heart valve structure using the principles of tissue engineering. The present approach aims to guide more mature tissue development in fibrin-based valves based on in vitro conditioning in a custom-designed bioreactor system. Moulded fibrin-based tissue-engineered heart valves seeded with ovine carotid artery-derived cells were subjected to 12 days of mechanical conditioning in a bioreactor system. The bioreactor pulse rate was increased from 5 to 10 b.p.m. after 6 days, while a pressure difference of 20 mmH(2)O was maintained over the valve leaflets. Control valves were cultured under stirred conditions in a beaker. Cell phenotype and extracellular matrix (ECM) composition were analysed in all samples and compared to native ovine aortic valve tissue using routine histological and immunohistochemical techniques. Conditioned valve leaflets showed reduced tissue shrinkage compared to stirred controls. Limited ECM synthesis was evident in stirred controls, while the majority of cells were detached from the fibrin scaffold. Dynamic conditioning increased cell attachment/alignment and expression of alpha-smooth muscle actin, while enhancing the deposition of ECM proteins, including types I and III collagen, fibronectin, laminin and chondroitin sulphate. There was no evidence for elastin synthesis in either stirred controls or conditioned samples. The present study demonstrates that the application of low-pressure conditions and increasing pulsatile flow not only enhances seeded cell attachment and alignment within fibrin-based heart valves, but dramatically changes the manner in which these cells generate ECM proteins and remodel the valve matrix. Optimised dynamic conditioning, therefore, might accelerate the maturation of surgically feasible and implantable autologous fibrin-based tissue-engineered heart valves. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3388 / 3397
页数:10
相关论文
共 30 条
[1]   Human semilunar cardiac valve remodeling by activated cells from fetus to adult - Implications for postnatal adaptation, pathology, and tissue engineering [J].
Aikawa, E ;
Whittaker, P ;
Farber, M ;
Mendelson, K ;
Padera, RF ;
Aikawa, M ;
Schoen, FJ .
CIRCULATION, 2006, 113 (10) :1344-1352
[2]   Sterilization, toxicity, biocompatibility and clinical applications of polylactic acid polyglycolic acid copolymers [J].
Athanasiou, KA ;
Niederauer, GG ;
Agrawal, CM .
BIOMATERIALS, 1996, 17 (02) :93-102
[3]   Bioreactors for cardiovascular cell and tissue growth: A review [J].
Barron, V ;
Lyons, E ;
Stenson-Cox, C ;
McHugh, PE ;
Pandit, A .
ANNALS OF BIOMEDICAL ENGINEERING, 2003, 31 (09) :1017-1030
[4]   AGE-RELATED COLLAGEN AND ELASTIN CONTENT OF HUMAN HEART VALVES [J].
BASHEY, RI ;
TORII, S ;
ANGRIST, A .
JOURNALS OF GERONTOLOGY, 1967, 22 (02) :203-&
[5]   COLLAGEN COMPOSITION OF NORMAL AND MYXOMATOUS HUMAN MITRAL HEART-VALVES [J].
COLE, WG ;
CHAN, D ;
HICKEY, AJ ;
WILCKEN, DEL .
BIOCHEMICAL JOURNAL, 1984, 219 (02) :451-460
[6]   Design of a new pulsatile bioreactor for tissue engineered aortic heart valve formation [J].
Dumont, K ;
Yperman, J ;
Verbeken, E ;
Segers, P ;
Meuris, B ;
Vandenberghe, S ;
Flameng, W ;
Verdonck, PR .
ARTIFICIAL ORGANS, 2002, 26 (08) :710-714
[7]   A collagen-glycosaminoglycan co-culture model for heart valve tissue engineering applications [J].
Flanagan, TC ;
Wilkins, B ;
Black, A ;
Jockenhoevel, S ;
Smith, TJ ;
Pandit, AS .
BIOMATERIALS, 2006, 27 (10) :2233-2246
[8]  
Flanagan Thomas C., 2003, European Cells & Materials, V6, P28
[9]  
Hoerstrup SP, 2000, CIRCULATION, V102, P44
[10]   Tissue engineering of functional trileaflet heart valves from human marrow stromal cells [J].
Hoerstrup, SP ;
Kadner, A ;
Melnitchouk, S ;
Trojan, A ;
Eid, K ;
Tracy, J ;
Sodian, R ;
Visjager, JF ;
Kolb, SA ;
Grunenfelder, J ;
Zund, G ;
Turina, MI .
CIRCULATION, 2002, 106 (13) :I143-I150