Nasal chondrocytes and fibrin sealant for cartilage tissue engineering

被引:53
作者
Vinatier, C. [1 ]
Gauthier, O. [1 ]
Masson, M. [1 ]
Malard, O. [1 ]
Moreau, A. [2 ]
Fellah, B. H. [1 ]
Bilban, M. [3 ]
Spaethe, R. [3 ]
Daculsi, G. [1 ]
Guicheux, J. [1 ]
机构
[1] Univ Nantes, Lab Osteoarticular & Dent Tissue Engn, INSERM, U791, F-44042 Nantes, France
[2] Univ Hosp, Dept Anatomocytopathol, Nantes, France
[3] Baxter Biosci Biosurg, Vienna, Austria
关键词
fibrin sealant; nasal chondrocytes; tissue engineering; articular cartilage; HUMAN ARTICULAR CHONDROCYTES; FULL-THICKNESS DEFECTS; OSTEOCHONDRAL DEFECTS; ENZYMATIC TREATMENT; REPAIR; GLUE; EXPRESSION; COLLAGEN; DIFFERENTIATION; INTEGRATION;
D O I
10.1002/jbm.a.31988
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Hybrid constructs associating a biodegradable matrix and autologous chondrocytes hold promise for the treatment of articular cartilage defects. In this context, our objective was to investigate the potential use of nasal chondrocytes associated with a fibrin sealant for the treatment of articular cartilage defects. The phenotype of primary nasal chondrocytes (NC) from human (HNC) and rabbit (RNC) origin were characterized by RT-PCR. The ability of constructs associating fibrin sealant and NC to form a cartilaginous tissue in vivo was investigated, firstly in a subcutaneous site in nude mice and secondly in an articular cartilage defect in rabbit. HNC express type 11 collagen and aggrecan, the two major hallmarks of a chondrocytic phenotype. Furthermore, when injected subcutaneously into nude mice within a fibrin sealant, these chondrocytes were able to form a cartilage-like tissue. Our data indicate that RNC also express type 11 collagen and aggrecan and maintained their phenotype in three-dimensional culture within a fibrin sealant. Moreover, treatment of rabbit articular cartilage defects with autologous RNC embedded in a fibrin sealant led to the formation of a hyalin-like repair tissue. The use of fibrin sealant containing hybrid autologous NC therefore appears as a promising approach for cell-based therapy of articular cartilage. (c) 2008 Wiley Periodicals, Inc. J Biomed Mater Res 89A: 176-185, 2009
引用
收藏
页码:176 / 185
页数:10
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