Department of Microgravity and Translational Regenerative Medicine, Clinic for Plastic, Aesthetic and Hand Surgery, Otto von Guericke University, 39106 Magdeburg, Germany.
Department for Biomedicine, Aarhus University, 8000 Aarhus, Denmark.
Int J Mol Sci. 2020 Dec 16;21(24):9596. doi: 10.3390/ijms21249596.
Articular cartilage is a skeletal tissue of avascular nature and limited self-repair capacity. Cartilage-degenerative diseases, such as osteoarthritis (OA), are difficult to treat and often necessitate joint replacement surgery. Cartilage is a tough but flexible material and relatively easy to damage. It is, therefore, of high interest to develop methods allowing chondrocytes to recolonize, to rebuild the cartilage and to restore joint functionality. Here we studied the in vitro production of cartilage-like tissue using human articular chondrocytes exposed to the Random Positioning Machine (RPM), a device to simulate certain aspects of microgravity on Earth. To screen early adoption reactions of chondrocytes exposed to the RPM, we performed quantitative real-time PCR analyses after 24 h on chondrocytes cultured in DMEM/F-12. A significant up-regulation in the gene expression of , , , , , , and was detected, while the levels of , , , , , , , , , , , and mRNAs remained unchanged. The STRING (Search Tool for the Retrieval of Interacting Genes/Proteins) analysis demonstrated among others the importance of these differentially regulated genes for cartilage formation. Chondrocytes grown in DMEM/F-12 medium produced three-dimensional (3D) spheroids after five days without the addition of scaffolds. On day 28, the produced tissue constructs reached up to 2 mm in diameter. Using specific chondrocyte growth medium, similar results were achieved within 14 days. Spheroids from both types of culture media showed the typical cartilage morphology with aggrecan positivity. Intermediate filaments form clusters under RPM conditions as detected by vimentin staining after 7 d and 14 d. Larger meshes appear in the network in 28-day samples. Furthermore, they were able to form a confluent chondrocyte monolayer after being transferred back into cell culture flasks in 1 conditions showing their suitability for transplantation into joints. Our results demonstrate that the cultivation medium has a direct influence on the velocity of tissue formation and tissue composition. The spheroids show properties that make them interesting candidates for cellular cartilage regeneration approaches in trauma and OA therapy.
关节软骨是一种无血管、自我修复能力有限的骨骼组织。软骨退行性疾病,如骨关节炎(OA),难以治疗,通常需要关节置换手术。软骨是一种坚韧但有弹性的材料,相对容易受损。因此,开发允许软骨细胞再殖民、重建软骨和恢复关节功能的方法具有重要意义。在这里,我们使用暴露于旋转定位机(RPM)的人关节软骨细胞研究了软骨样组织的体外生产,RPM 是一种模拟地球上微重力某些方面的设备。为了筛选暴露于 RPM 的软骨细胞的早期采用反应,我们在 DMEM/F-12 中培养的软骨细胞培养 24 小时后进行了定量实时 PCR 分析。检测到基因表达的显著上调 、 、 、 、 、 和 ,而 、 、 、 、 、 、 、 和 mRNA 的水平保持不变。STRING(搜索检索相互作用基因/蛋白的工具)分析表明,这些差异调节基因对软骨形成非常重要。在没有添加支架的情况下,在 DMEM/F-12 培养基中生长的软骨细胞在五天后产生三维(3D)球体。在第 28 天,产生的组织构建体直径达到 2 毫米。在使用特定的软骨细胞生长培养基的情况下,在 14 天内也可以获得类似的结果。来自两种类型培养基的球体都显示出典型的软骨形态,具有聚集蛋白阳性。在 RPM 条件下,中间丝通过波形蛋白染色在 7d 和 14d 后形成簇。在 28 天的样本中出现更大的网格。此外,它们在转移回细胞培养瓶中 1 条件下能够形成连续的软骨细胞单层,显示出它们适合移植到关节中。我们的结果表明,培养培养基直接影响组织形成的速度和组织组成。球体显示出使其成为创伤和 OA 治疗中细胞软骨再生方法的有趣候选物的特性。