首页> 外文期刊>In Vitro Cellular and Developmental Biology. Animal: Journal of the Tissues Culture Association >IN VITRO COMPARISON OF SIX DIFFERENT MATRIX SYSTEMS FOR THE CULTIVATION OF HUMAN CHONDROCYTES
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IN VITRO COMPARISON OF SIX DIFFERENT MATRIX SYSTEMS FOR THE CULTIVATION OF HUMAN CHONDROCYTES

机译:六种不同基质系统在体外培养人软骨细胞的体外比较

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摘要

In recent years, a great variety of different matrix systems for the cultivation of chondrocytes have been developed. Although some of these scaffolds show promising experimental results in vitro, the potential clinical value remains unclear. In thiscomparative study, we propagated human articular chondrocytes precultivated in monolayer culture on six different scaffolds (collagen gels, membranes and sponges) under standardized in vitro conditions. Mechanical properties of the matrix systems were not improved significantly by cultivation of human chondrocytes under the given in vitro conditions. The gel systems (CaReS, Ars Artho, Germany and Atelocollagen, Koken, Japan) showed a homogeneous cell distribution; chondrocytes propagated on Chondro-Gide(Geistlich Biomaterials, Switzerland) and Integra membranes (Integra, USA) were building multilayers. Only few cells penetrated the two Atelocollagen honeycomb sponges (Koken, Japan). During cultivation, chondrocytes propagated on all systems showed a partial morphological redifferentiation, which was best with regard to the gel systems. In general, only small amounts of collagen type-II protein could be detected in the pericellular region and chondrocytes failed to build a territorial matrix. During the first two weeks of cultivation, the two gel systems showed a significantly higher collagen type-II gene expression and a lower collagen type-I gene expression than the other investigated matrix systems. Although collagen gels seem to be superior whendealing with deep cartilage defects, membrane systems might rather be useful in improving conventional autologous chondrocyte transplantation or in combination with gel systems.
机译:近年来,已经开发出多种用于培养软骨细胞的不同基质系统。尽管其中一些支架在体外显示出令人鼓舞的实验结果,但潜在的临床价值仍不清楚。在这项比较研究中,我们在标准化的体外条件下,在六个不同的支架(胶原蛋白凝胶,膜和海绵)上繁殖了单层培养物中预培养的人关节软骨细胞。通过在给定的体外条件下培养人软骨细胞,基质系统的机械性能没有得到明显改善。凝胶系统(德国的Ars Artho的CaReS和日本的Koken的Atelocollagen)显示出均匀的细胞分布。在Chondro-Gide(Geistlich Biomaterials,瑞士)和Integra膜(Integra,美国)上繁殖的软骨细胞正在构建多层膜。只有很少的细胞穿透了两个Atelocollagen蜂窝海绵(日本Koken)。在培养过程中,在所有系统上繁殖的软骨细胞均表现出部分形态上的再分化,这对于凝胶系统而言是最好的。通常,在细胞周围区域只能检测到少量的II型胶原蛋白,而软骨细胞无法建立领土基质。在培养的前两周中,两个凝胶系统显示出比其他研究的基质系统明显更高的II型胶原基因表达和更低的I型胶原基因表达。尽管胶原蛋白凝胶在处理软骨深部缺损时似乎更胜一筹,但膜系统可能更有助于改善传统的自体软骨细胞移植或与凝胶系统结合使用。

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