A novel culture device for the evaluation of three-dimensional extracellular matrix materials

被引:3
|
作者
Akhyari, Payam [1 ,2 ,3 ]
Ziegler, Heiko [1 ,3 ]
Gwanmesia, Patricia [3 ]
Barth, Mareike [4 ]
Schilp, Soeren [5 ]
Huelsmann, Joern [2 ]
Hoffmann, Stefanie [3 ]
Bosch, Julia [6 ]
Koegler, Gesine [6 ]
Lichtenberg, Artur [1 ,2 ]
机构
[1] Dusseldorf Univ Hosp, Dept Cardiovasc Surg, D-40225 Dusseldorf, Germany
[2] Dusseldorf Univ Hosp, Inst Expt Surg, D-40225 Dusseldorf, Germany
[3] Univ Heidelberg Hosp, Dept Cardiac Surg, Heidelberg, Germany
[4] German Canc Res Ctr, Helmholtz Grp Cell Biol, Heidelberg, Germany
[5] Heidelberg Univ, Inst Appl Phys Chem, D-69115 Heidelberg, Germany
[6] Dusseldorf Univ Hosp, Inst Transplantat Diagnost & Cell Therapeut, D-40225 Dusseldorf, Germany
关键词
extracellular matrix; coating; in vitro culture; custom-made culture device; 3D culture; cell-matrix interaction; endothelial cell; heart valve leaflet; ENGINEERED HEART-VALVES; RE-ENDOTHELIALIZATION; TISSUE; GRAFTS; CELLS;
D O I
10.1002/term.1550
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cell-matrix interactions in a three-dimensional (3D) extracellular matrix (ECM) are of fundamental importance in living tissue, and their in vitro reconstruction in bioartificial structures represents a core target of contemporary tissue engineering concepts. For a detailed analysis of cell-matrix interaction under highly controlled conditions, we developed a novel ECM evaluation culture device (EECD) that allows for a precisely defined surface-seeding of 3D ECM scaffolds, irrespective of their natural geometry. The effectiveness of EECD was evaluated in the context of heart valve tissue engineering. Detergent decellularized pulmonary cusps were mounted in EECD and seeded with endothelial cells (ECs) to study EC adhesion, morphology and function on a 3D ECM after 3, 24, 48 and 96 h. Standard EC monolayers served as controls. Exclusive top-surface-seeding of 3D ECM by viable ECs was demonstrated by laser scanning microscopy (LSM), resulting in a confluent re-endothelialization of the ECM after 96 h. Cell viability and protein expression, as demonstrated by MTS assay and western blot analysis (endothelial nitric oxide synthase, von Willebrand factor), were preserved at maintained levels over time. In conclusion, EECD proves as a highly effective system for a controlled repopulation and in vitro analysis of cell-ECM interactions in 3D ECM. Copyright (C) 2012 John Wiley & Sons, Ltd.
引用
收藏
页码:673 / 681
页数:9
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