Pharmaceutical Production Research Facility, Schulich School of Engineering, University of Calgary, Calgary, Canada.
McCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, Calgary, Canada.
J Tissue Eng Regen Med. 2018 Mar;12(3):e1418-e1432. doi: 10.1002/term.2531. Epub 2017 Dec 12.
Osteoarthritis (OA) is a painful disease, characterized by progressive surface erosion of articular cartilage. The use of human articular chondrocytes (hACs) sourced from OA patients has been proposed as a potential therapy for cartilage repair, but this approach is limited by the lack of scalable methods to produce clinically relevant quantities of cartilage-generating cells. Previous studies in static culture have shown that hACs co-cultured with human mesenchymal stem cells (hMSCs) as 3D pellets can upregulate proliferation and generate neocartilage with enhanced functional matrix formation relative to that produced from either cell type alone. However, because static culture flasks are not readily amenable to scale up, scalable suspension bioreactors were investigated to determine if they could support the co-culture of hMSCs and OA hACs under serum-free conditions to facilitate clinical translation of this approach. When hACs and hMSCs (1:3 ratio) were inoculated at 20,000 cells/ml into 125-ml suspension bioreactors and fed weekly, they spontaneously formed 3D aggregates and proliferated, resulting in a 4.75-fold increase over 16 days. Whereas the apparent growth rate was lower than that achieved during co-culture as a 2D monolayer in static culture flasks, bioreactor co-culture as 3D aggregates resulted in a significantly lower collagen I to II mRNA expression ratio and more than double the glycosaminoglycan/DNA content (5.8 vs. 2.5 μg/μg). The proliferation of hMSCs and hACs as 3D aggregates in serum-free suspension culture demonstrates that scalable bioreactors represent an accessible platform capable of supporting the generation of clinical quantities of cells for use in cell-based cartilage repair.
骨关节炎(OA)是一种疼痛性疾病,其特征为关节软骨进行性表面侵蚀。使用源自 OA 患者的人关节软骨细胞(hAC)已被提议作为软骨修复的潜在治疗方法,但这种方法受到缺乏可规模化生产具有临床相关性的软骨生成细胞的限制。先前在静态培养中的研究表明,与单独使用任何一种细胞类型相比,共培养于 3D 微球中的 hAC 与人间质干细胞(hMSC)可以上调增殖并生成具有增强功能基质形成的新软骨。然而,由于静态培养瓶不易规模化,因此研究了可规模化的悬浮生物反应器,以确定它们是否可以在无血清条件下支持 hMSC 和 OA hAC 的共培养,从而促进该方法的临床转化。当 hAC 和 hMSC(1:3 比例)以 20,000 个细胞/ml 接种到 125-ml 悬浮生物反应器中并每周进行喂养时,它们会自发形成 3D 聚集体并增殖,在 16 天内增长了 4.75 倍。虽然表观生长率低于在静态培养瓶中作为 2D 单层进行共培养时的生长率,但作为 3D 聚集体的生物反应器共培养导致胶原 I 与 II 的 mRNA 表达比例显著降低,糖胺聚糖/DNA 含量增加了两倍多(5.8 比 2.5μg/μg)。hMSC 和 hAC 在无血清悬浮培养中的 3D 聚集体增殖表明,可规模化的生物反应器代表了一种可接近的平台,能够支持用于基于细胞的软骨修复的临床数量的细胞的生成。