Anders J O, Mollenhauer J, Beberhold A, Kinne R W, Venbrocks R A
Department of Orthopaedics, University Hospital, Jena, Germany.
J Bone Joint Surg Br. 2009 Mar;91(3):409-16. doi: 10.1302/0301-620X.91B3.20869.
The gelatin-based haemostyptic compound Spongostan was tested as a three-dimensional (3D) chondrocyte matrix in an in vitro model for autologous chondrocyte transplantation using cells harvested from bovine knees. In a control experiment of monolayer cultures, the proliferation or de-differentiation of bovine chondrocytes was either not or only marginally influenced by the presence of Spongostan (0.3 mg/ml). In monolayers and 3-D Minusheet culture chambers, the cartilage-specific differentiation markers aggrecan and type-II collagen were ubiquitously present in a cell-associated fashion and in the pericellular matrix. The Minusheet cultures usually showed a markedly higher mRNA expression than monolayer cultures irrespective of whether Spongostan had been present or not during culture. Although the de-differentiation marker type-I collagen was also present, the ratio of type-I to type-II collagen or aggrecan to type-I collagen remained higher in Minusheet 3-D cultures than in monolayer cultures irrespective of whether Spongostan had been included in or excluded from the monolayer cultures. The concentration of GAG in Minusheet cultures reached its maximum after 14 days with a mean of 0.83 +/- 0.8 microg/10(6) cells; mean +/-, SEM, but remained considerably lower than in monolayer cultures with/without Spongostan. Our results suggest that Spongostan is in principle suitable as a 3-D chondrocyte matrix, as demonstrated in Minusheet chambers, in particular for a culture period of 14 days. Clinically, differentiating effects on chondrocytes, simple handling and optimal formability may render Spongostan an attractive 3-D scaffold for autologous chondrocyte transplantation.
以明胶为基础的止血化合物海绵明胶,在一个使用从牛膝关节采集的细胞进行自体软骨细胞移植的体外模型中,被测试作为三维(3D)软骨细胞基质。在单层培养的对照实验中,海绵明胶(0.3毫克/毫升)的存在对牛软骨细胞的增殖或去分化没有影响或仅有轻微影响。在单层培养和三维Minusheet培养室中,软骨特异性分化标志物聚集蛋白聚糖和II型胶原以细胞相关的方式普遍存在于细胞周围基质中。无论培养过程中是否存在海绵明胶,Minusheet培养通常比单层培养显示出明显更高的mRNA表达。尽管去分化标志物I型胶原也存在,但无论单层培养中是否包含海绵明胶,Minusheet三维培养中I型与II型胶原的比例或聚集蛋白聚糖与I型胶原的比例仍高于单层培养。Minusheet培养中糖胺聚糖(GAG)的浓度在14天后达到最大值,平均为0.83±0.8微克/10(6)个细胞;平均值±标准误,但仍远低于有/无海绵明胶的单层培养。我们的结果表明,海绵明胶原则上适合作为三维软骨细胞基质,如在Minusheet培养室中所证明的,特别是在14天的培养期内。临床上,对软骨细胞的分化作用、简单的操作和最佳的可成型性可能使海绵明胶成为自体软骨细胞移植的有吸引力的三维支架。