3D ingrowth of bovine articular chondrocytes in biodegradable cryogel scaffolds for cartilage tissue engineering

被引:33
作者
Bolgen, N. [1 ]
Yang, Y. [2 ]
Korkusuz, P. [3 ]
Guzel, E. [4 ]
El Haj, A. J. [2 ]
Piskin, E. [5 ,6 ,7 ]
机构
[1] Mersin Univ, Fac Engn, Dept Chem Engn, TR-33343 Mersin, Turkey
[2] Keele Univ, Inst Sci & Technol Med, Stoke On Trent ST4 7QB, Staffs, England
[3] Hacettepe Univ, Fac Med, Dept Histol & Embryol, TR-06100 Ankara, Turkey
[4] Istanbul Univ, Dept Histol & Embryol, Cerrahpasa Med Fac, Istanbul, Turkey
[5] Hacettepe Univ, Dept Chem Engn, TR-06800 Ankara, Turkey
[6] Hacettepe Univ, Bioengn Div, TR-06800 Ankara, Turkey
[7] Hacettepe Univ, Ctr Bioengn & Biomedtech, TR-06800 Ankara, Turkey
关键词
cartilage tissue engineering; biodegradable cryogel scaffolds; HEMA-lactate-dextran; bovine articular chondrocytes; BONE; HYDROGELS; MATRICES; DEGRADATION; EXPRESSION; DEFECTS; CULTURE; REPAIR; CELLS;
D O I
10.1002/term.375
中图分类号
Q813 [细胞工程];
学科分类号
摘要
A feasibility study was undertaken to examine the potential of biodegradable HEMA-lactate-dextran (HEMA-LLA-D)-based cryogels as scaffolds for cartilage tissue engineering. This was a preliminary in vitro study giving essential information on the biocompatibility of cryogels with cartilage cells. HEMA-lactate (HEMA-LLA) and HEMA-LLA-D were synthesized and characterized by different techniques. Cryogel scaffolds with supermacroporous structures were produced by cryogenic treatment of these macromers. Chondrocytes obtained from bovine articular cartilage were seeded onto cylindrical cryogels and cultured. The samples were examined by several microcopical techniques for cell viability and morphological analyses were performed at two culture points. Histological study of the constructs revealed the cells' growth on the surface and within the scaffolds. Confocal microscopical images demonstrated that the majority of live vs. dead cells had been attached to and integrated with the pores of the scaffold. SEM analysis showed round to oval-shaped chondrocytic cells interconnected with each other by communicating junctions. The chondrocytes rapidly proliferated in the cryogels, manifesting that they fully covered the scaffold surface after 9 days and almost filled the spaces in the pores of the scaffold after 15 days of culture. Chondrocytes secreted significant amount of extracellular matrix in the scaffolds and exhibited highly interconnective morphology. Light and transmission electron microscopy revealed groups of active cartilage cells closely apposed to the cryogel. We concluded that cryogel scaffolds could be excellent candidates for cartilage tissue regeneration with their extraordinary properties, including soft, elastic nature, highly open interconnected pore structure and very rapid, controllable swellability. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:770 / 779
页数:10
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