Chen A C, Nagrampa J P, Schinagl R M, Lottman L M, Sah R L
Department of Bioengineering, University of California, San Diego, La Jolla 92093-0412, USA.
J Orthop Res. 1997 Nov;15(6):791-802. doi: 10.1002/jor.1100150602.
The transplantation of chondrocytes has shown promise for augmenting the repair of defects in articular cartilage. This in vitro study examined the efficiency of the transplantation of bovine chondrocytes onto articular cartilage disks and the ability of the transplanted chondrocytes to subsequently synthesize and deposit proteoglycan. The radiolabeling of chondrocyte cultures with [3H]thymidine, followed by 4 days of chase incubation, resulted in the incorporation of 98% of the radiolabel into DNA (as assessed by susceptibility to DNase). At the end of the culture period, the [3H]DNA was stable, with a half-life of radioactivity loss into the medium of 73 days. With use of radiolabeled chondrocytes for quantitation, the efficiency of transplantation onto a cartilage substrate was 93 +/- 4% for seeding densities of as much as 650,000 cells per cm2 and a seeding duration of 1 hour. These findings were confirmed both by tracking cells stained with 5-chlormethylfluorescein diacetate and by quantitating DNA. During the 16 hours after seeding onto a cartilage substrate (in which the endogenous cells had been lysed by lyophilization), the transplanted cells synthesized sulfated proteoglycan in direct proportion to the number of cells seeded. Most (83%) of the newly synthesized proteoglycan was released into the medium rather than retained within the layer of transplanted cells and the recipient cartilage substrate. Comparative studies with lyophilized-rehydrated or live cartilage as the recipient substrate indicated a similar efficiency of chondrocyte seeding and proteoglycan synthesis by the seeded chondrocytes. The transplanted cells retained the chondrocyte phenotype, as judged by a high proportion of the [35S]macromolecules being in the form of aggrecan that was capable of aggregating with hyaluronan and link protein, as well as by immunostaining within and around the transplanted cells for type-II, but not type-I, collagen. These results indicate that the number of chondrocytes transplanted onto a cut cartilage surface greatly affects the level of matrix synthesis; this in turn may affect repair.
软骨细胞移植已显示出增强关节软骨缺损修复的前景。这项体外研究检测了将牛软骨细胞移植到关节软骨盘上的效率,以及移植后的软骨细胞随后合成和沉积蛋白聚糖的能力。用[3H]胸苷对软骨细胞培养物进行放射性标记,随后进行4天的追踪培养,结果98%的放射性标记物掺入了DNA(通过对DNase的敏感性评估)。在培养期结束时,[3H]DNA稳定,放射性物质向培养基中损失的半衰期为73天。使用放射性标记的软骨细胞进行定量分析,对于每平方厘米高达650,000个细胞的接种密度和1小时的接种持续时间,移植到软骨基质上的效率为93±4%。通过追踪用5-氯甲基荧光素二乙酸酯染色的细胞以及定量DNA,这些结果均得到了证实。在接种到软骨基质上(其中内源性细胞已通过冻干裂解)后的16小时内,移植细胞合成硫酸化蛋白聚糖的量与接种的细胞数量成正比。大多数(83%)新合成的蛋白聚糖释放到培养基中,而不是保留在移植细胞层和受体软骨基质内。以冻干复水或活软骨作为受体基质的比较研究表明,接种的软骨细胞在软骨细胞接种和蛋白聚糖合成方面具有相似的效率。通过高比例的[35S]大分子以能够与透明质酸和连接蛋白聚集的聚集蛋白聚糖形式存在,以及通过对移植细胞内外进行II型而非I型胶原蛋白的免疫染色判断,移植细胞保留了软骨细胞表型。这些结果表明,移植到切割软骨表面的软骨细胞数量极大地影响基质合成水平;这反过来可能影响修复。