The remodeling of cardiovascular bioprostheses under influence of stem cell homing signal pathways

被引:27
作者
De Visscher, Geofrey [1 ]
Lebacq, An [1 ]
Mesure, Lindsay [1 ]
Blockx, Helga [1 ]
Vranken, Ilse [1 ]
Plusquin, Ruth [1 ]
Meuris, Bart [1 ]
Herregods, Marie-Christine [2 ]
Van Oosterwyck, Hans [3 ]
Flameng, Willem [1 ]
机构
[1] Katholieke Univ Leuven, Dept Cardiovasc Dis, Lab Expt Cardiac Surg, B-3000 Louvain, Belgium
[2] Katholieke Univ Leuven, Div Cardiol, B-3000 Louvain, Belgium
[3] Katholieke Univ Leuven, Div Biomech & Engn Design, B-3000 Louvain, Belgium
关键词
Bioprosthesis; Cell adhesion; Fibronectin; Heart valve & Vascular grafts; PROGENITOR CELLS; BONE-MARROW; IN-VIVO; VALVE; MATRIX; CALCIFICATION; EXPRESSION; RECEPTOR; REPAIR; TOOL;
D O I
10.1016/j.biomaterials.2009.09.016
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Optimizing current heart valve replacement strategies by creating living prostheses is a necessity to alleviate complications with current bioprosthetic devices such as calcification and degeneration. Regenerative medicine, mostly in vitro tissue engineering, is the forerunner of this optimization search, yet here we show the functionality of an in vivo alternative making use of 2 homing axes for stem cells. in rats we studied the signaling pathways of stem cells on implanted bioprosthetic tissue (photooxidized bovine pericardium (POP)), by gene and protein expression analysis. We found that SDF-1 alpha/CXCR4 and FN/VLA4 homing axes play a role. When we implanted vascular grafts impregnated with SDF-1 alpha and/or FN as carotid artery interpositions, primitive cells were attracted from the circulation. Next, bioprosthetic heart valves, constructed from POP impregnated with SDF-1 alpha and/or FN, were implanted in pulmonary position. As shown by CD90, CD34 and CD117 immunofluorescent staining they became completely recellularized after 5 months, had a normal function and biomechanical properties and specifically the combination of SDF-1 alpha and FN had an optimal valve-cell phenotype. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
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