Department of Surgery, University Hospital Basel, Basel, Switzerland.
Biomaterials. 2010 Mar;31(8):2252-9. doi: 10.1016/j.biomaterials.2009.11.110.
In this study, we aimed at developing and validating a technique for the engineering of osteochondral grafts based on the biological bonding of a chondral layer with a bony scaffold by cell-laid extracellular matrix. Osteochondral composites were generated by combining collagen-based matrices (Chondro-Gide) containing human chondrocytes with devitalized spongiosa cylinders (Tutobone) using a fibrin gel (Tisseel). We demonstrate that separate pre-culture of the chondral layer for 3 days prior to the generation of the composite allows for (i) more efficient cartilaginous matrix accumulation than no pre-culture, as assessed histologically and biochemically, and (ii) superior biological bonding to the bony scaffold than 14 days of pre-culture, as assessed using a peel-off mechanical test, developed to measure integration of bilayered materials. The presence of the bony scaffold induced an upregulation in the infiltrated cells of the osteoblast-related gene bone sialoprotein, indicative of the establishment of a gradient of cell phenotypes, but did not affect per se the quality of the cartilaginous matrix in the chondral layer. The described strategy to generate osteochondral plugs is simple to be implemented and--since it is based on clinically compliant cells and materials--is amenable to be readily tested in the clinic.
在这项研究中,我们旨在开发和验证一种基于细胞外基质的生物结合技术,用于构建骨软骨移植物,即将软骨层与骨支架结合。通过使用纤维蛋白凝胶(Tisseel)将含有人类软骨细胞的基于胶原蛋白的基质(Chondro-Gide)与脱细胞海绵骨圆柱体(Tutobone)相结合,生成骨软骨复合材料。我们证明,在生成复合材料之前,对软骨层进行 3 天的预培养,可以(i)比不进行预培养更有效地积累软骨基质,这可以通过组织学和生物化学评估,以及(ii)通过开发的剥离机械测试评估,比 14 天的预培养更好地与骨支架结合,该测试用于测量双层材料的整合。骨支架的存在诱导浸润细胞中骨涎蛋白相关基因的上调,表明细胞表型梯度的建立,但本身并不影响软骨层中软骨基质的质量。描述的生成骨软骨塞的策略易于实施,并且由于它基于临床相容的细胞和材料,因此易于在临床中进行测试。