Ibold Yvonne, Frauenschuh Simone, Kaps Christian, Sittinger Michael, Ringe Jochen, Goetz Peter M
Department of Bioprocess Engineering, Institute of Biotechnology, Technical University of Berlin, Germany.
J Biomol Screen. 2007 Oct;12(7):956-65. doi: 10.1177/1087057107307147.
The 3-dimensional (3-D) pannus model for rheumatoid arthritis (RA) is based on the interactive co-culture of cartilage and synovial fibroblasts (SFs). Besides the investigation of the pathogenesis of RA, it can be used to analyze the active profiles of antirheumatic pharmaceuticals and other bioactive substances under in vitro conditions. For a potential application in the industrial drug-screening process as a transitional step between 2-dimensional (2-D) cell-based assays and in vivo animal studies, the pannus model was developed into an in vitro high-throughput screening (HTS) assay. Using the CyBitrade mark-Disk workstation for parallel liquid handling, the main cell culture steps of cell seeding and cultivation were automated. Chondrocytes were isolated from articular cartilage and seeded directly into 96-well microplates in high-density pellets to ensure formation of cartilage-specific extracellular matrix (ECM). Cell seeding was performed automatically and manually to compare both processes regarding accuracy, reproducibility, consistency, and handling time. For automated cultivation of the chondrocyte pellet cultures, a sequential program was developed using the CyBio Control software to minimize shear forces and handling time. After 14 days of cultivation, the pannus model was completed by coating the cartilage pellets with a layer of human SFs. The effects due to automation in comparison to manual handling were analyzed by optical analysis of the pellets, histological and immunohistochemical staining, and real-time PCR. Automation of this in vitro model was successfully achieved and resulted in an improved quality of the generated pannus cultures by enhancing the formation of cartilage-specific ECM. In addition, automated cell seeding and media exchange increased the efficiency due to a reduction of labor intensity and handling time.
类风湿关节炎(RA)的三维(3-D)血管翳模型基于软骨与滑膜成纤维细胞(SFs)的交互式共培养。除了用于研究RA的发病机制外,它还可用于在体外条件下分析抗风湿药物和其他生物活性物质的活性概况。为了在工业药物筛选过程中作为二维(2-D)细胞检测和体内动物研究之间的过渡步骤进行潜在应用,血管翳模型被开发成一种体外高通量筛选(HTS)检测方法。使用CyBitrade mark-Disk工作站进行平行液体处理,细胞接种和培养的主要细胞培养步骤实现了自动化。从关节软骨中分离软骨细胞,并以高密度沉淀的形式直接接种到96孔微孔板中,以确保形成软骨特异性细胞外基质(ECM)。分别自动和手动进行细胞接种,以比较这两个过程在准确性、可重复性、一致性和操作时间方面的差异。为了自动培养软骨细胞沉淀培养物,使用CyBio Control软件开发了一个顺序程序,以尽量减少剪切力和操作时间。培养14天后,通过在软骨沉淀上覆盖一层人SFs来完成血管翳模型。通过对沉淀进行光学分析、组织学和免疫组织化学染色以及实时PCR,分析了与手动操作相比自动化带来的影响。该体外模型成功实现了自动化,通过增强软骨特异性ECM的形成提高了所生成的血管翳培养物的质量。此外,自动细胞接种和培养基更换由于降低了劳动强度和操作时间而提高了效率。