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 10 条
  • [1] Development of fibrin-based tissue engineered vessels
    Swartz, DD
    Russell, J
    Andreadis, S
    SECOND JOINT EMBS-BMES CONFERENCE 2002, VOLS 1-3, CONFERENCE PROCEEDINGS: BIOENGINEERING - INTEGRATIVE METHODOLOGIES, NEW TECHNOLOGIES, 2002, : 868 - 870
  • [2] A New Bioreactor for the Development of Tissue-Engineered Heart Valves
    Ruel, Jean
    Lachance, Genevieve
    ANNALS OF BIOMEDICAL ENGINEERING, 2009, 37 (04) : 674 - 681
  • [3] A New Bioreactor for the Development of Tissue-Engineered Heart Valves
    Jean Ruel
    Geneviève Lachance
    Annals of Biomedical Engineering, 2009, 37 : 674 - 681
  • [4] Textile Reinforcement in Fibrin-based Tissue Engineerd Heart Valves
    Ross, R.
    Salein, J.
    Menne, M.
    Mela, P.
    Jockenhoevel, S.
    Gries, T.
    BIOMEDICAL ENGINEERING-BIOMEDIZINISCHE TECHNIK, 2013, 58
  • [5] Development and Evaluation of a Tissue-Engineered Fibrin-based Canine Mitral Valve Three-dimensional Cell Culture System
    Liu, M-M
    Flanagan, T. C.
    Jockenhovel, S.
    Black, A.
    Lu, C-C
    French, A. T.
    Argyle, D. J.
    Corcoran, B. M.
    JOURNAL OF COMPARATIVE PATHOLOGY, 2018, 160 : 23 - 33
  • [6] ENDOTHELIAL PROGENITOR CELLS OVEREXPRESSING GRB2-ASSOCIATED BINDER 1 FOR IN VITRO-CONSTRUCTED TISSUE-ENGINEERED HEART VALVES
    Zhang, Liyu
    Zuo, Jianxin
    Huang, Siyang
    Chang, Qing
    KARDIOLOGIYA, 2022, 62 (07) : 38 - 43
  • [7] Injectable living marrow stromal cell-based autologous tissue engineered heart valves: first experiences with a one-step intervention in primates
    Weber, Benedikt
    Scherman, Jacques
    Emmert, Maximilian Y.
    Gruenenfelder, Juerg
    Verbeek, Renier
    Bracher, Mona
    Black, Melanie
    Kortsmit, Jeroen
    Franz, Thomas
    Schoenauer, Roman
    Baumgartner, Laura
    Brokopp, Chad
    Agarkova, Irina
    Wolint, Petra
    Zund, Gregor
    Falk, Volkmar
    Zilla, Peter
    Hoerstrup, Simon P.
    EUROPEAN HEART JOURNAL, 2011, 32 (22) : 2830 - 2840
  • [8] Development of in vivo, Tissue-Engineered, Autologous, 3D Heart Valvular Tissue, Type SC Biovalve With Excellent Mechanical Properties, Valular Functions, and in vivo Performances
    Nakayama, Yasuhide
    Takewa, Yoshiaki
    Moriwaki, Takeshi
    Sumikura, Hirohito
    Miyamoto, Shinji
    Okamoto, Keitaro
    Funayama, Marina
    Furukoshi, Maya
    Tatsumi, Eisuke
    CIRCULATION, 2015, 132
  • [9] In vitro fabrication of autologous living tissue-engineered vascular grafts based on prenatally harvested ovine amniotic fluid-derived stem cells
    Weber, Benedikt
    Kehl, Debora
    Bleul, Ulrich
    Behr, Luc
    Sammut, Sebastien
    Frese, Laura
    Ksiazek, Agnieszka
    Achermann, Josef
    Stranzinger, Gerald
    Robert, Jerome
    Sanders, Bart
    Sidler, Michele
    Brokopp, Chad E.
    Proulx, Steven T.
    Frauenfelder, Thomas
    Schoenauer, Roman
    Emmert, Maximilian Y.
    Falk, Volkmar
    Hoerstrup, Simon P.
    JOURNAL OF TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2016, 10 (01) : 52 - 70
  • [10] Development of a Novel Human Cell-Derived Tissue-Engineered Heart Valve for Transcatheter Aortic Valve Replacement: an In Vitro and In Vivo Feasibility Study
    Lintas, V.
    Fioretta, E. S.
    Motta, S. E.
    Dijkman, P. E.
    Pensalfini, M.
    Mazza, E.
    Caliskan, E.
    Rodriguez, H.
    Lipiski, M.
    Sauer, M.
    Cesarovic, N.
    Hoerstrup, S. P.
    Emmert, M. Y.
    JOURNAL OF CARDIOVASCULAR TRANSLATIONAL RESEARCH, 2018, 11 (06) : 470 - 482