Engineering of fibrillar decorin matrices for a tissue-engineered trachea

被引:62
作者
Hinderer, Svenja [1 ,2 ,3 ,4 ]
Schesny, Marianne [1 ,2 ,3 ]
Bayrak, Alexandra [5 ]
Ibold, Bettina [5 ]
Hampel, Martina [4 ]
Walles, Thorsten [6 ]
Stock, Ulrich A. [7 ]
Seifert, Martina [5 ]
Schenke-Layland, Katja [1 ,2 ,3 ]
机构
[1] Fraunhofer Inst Interfacial Engn & Biotechnol IGB, Dept Cell & Tissue Engn, D-70569 Stuttgart, Germany
[2] Univ Hosp UKT, Dept Thorac & Cardiovasc Surg, D-72076 Tubingen, Germany
[3] Univ Tubingen, Interuniv Ctr Med Technol Stuttgart Tubingen IZST, D-72076 Tubingen, Germany
[4] Univ Stuttgart, Inst Interfacial Engn IGVT, D-70596 Stuttgart, Germany
[5] Charite, Inst Med Immunol, Berlin Brandenburg Ctr Regenerat Therapies BCRT, D-13353 Berlin, Germany
[6] Univ Hosp Wurzburg, Dept Cardiothorac & Thorac Vasc Surg, Wurzburg, Germany
[7] Goethe Univ Frankfurt, Dept Thorac & Cardiovasc Surg, Univ Hosp, D-60590 Frankfurt, Germany
关键词
Tissue engineering; Biomedical applications; Extracellular matrix; Electrospinning; Trachea; EXTRACELLULAR-MATRIX; HEART-VALVES; IN-VITRO; TRANSPLANTATION; CELLS; GRAFTS; FIBERS;
D O I
10.1016/j.biomaterials.2012.03.075
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Decorin is a structural and functional proteoglycan (PG) residing in the complex network of extracellular matrix (ECM) proteins in many connective tissues. Depending on the protein core and the glycosaminoglycan chain, PGs support cell adhesion, migration, proliferation, differentiation, ECM assembly and growth factor binding. For applications in tissue engineering, it is crucial to develop reliable, ECM-mimicking biomaterials. Electrospinning is a suitable method for creating three-dimensional (3D), fibrillar scaffolds. While there are numerous reports on the electrospinning of proteins including collagen, to date, there are no reports on the electrospinning of PGs. In the following study, we used electrospinning to generate decorin-containing matrices for tracheal tissue engineering applications. The electrospun scaffolds were analyzed using scanning electron microscopy, atomic force microscopy, contact angle measurements and dynamic mechanical analysis. Additionally, we confirmed PG functionality with immunostaining and 1,9-dimethylmethylene blue. To determine cell-matrix-interactions, tracheal cells (hPAECs) were seeded and analyzed using an FOXJ1-antibody. Moreover, interactions of the electrospun scaffolds with immune-mediated mechanisms were analyzed in detail. To conclude, we demonstrated the feasibility of electrospinning of decorin to generate functional 3D scaffolds with low immunogenicity for hPAEC expansion. Our data suggest that these hybrid materials may be suitable as a substrate for tracheal tissue engineering. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5259 / 5266
页数:8
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