Prometheus Division of Skeletal Tissue Engineering, KU Leuven, Leuven, Belgium.
Skeletal Biology and Engineering Research Center, Department of Development and Regeneration, KU Leuven, Leuven.
Stem Cells Transl Med. 2024 Mar 15;13(3):278-292. doi: 10.1093/stcltm/szad091.
Automated technologies are attractive for enhancing the robust manufacturing of tissue-engineered products for clinical translation. In this work, we present an automation strategy using a robotics platform for media changes, and imaging of cartilaginous microtissues cultured in static microwell platforms. We use an automated image analysis pipeline to extract microtissue displacements and morphological features as noninvasive quality attributes. As a result, empty microwells were identified with a 96% accuracy, and dice coefficient of 0.84 for segmentation. Design of experiment are used for the optimization of liquid handling parameters to minimize empty microwells during long-term differentiation protocols. We found no significant effect of aspiration or dispension speeds at and beyond manual speed. Instead, repeated media changes and time in culture were the driving force or microtissue displacements. As the ovine model is the preclinical model of choice for large skeletal defects, we used ovine periosteum-derived cells to form cartilage-intermediate microtissues. Increased expression of COL2A1 confirms chondrogenic differentiation and RUNX2 shows no osteogenic specification. Histological analysis shows an increased secretion of cartilaginous extracellular matrix and glycosaminoglycans in larger microtissues. Furthermore, microtissue-based implants are capable of forming mineralized tissues and bone after 4 weeks of ectopic implantation in nude mice. We demonstrate the development of an integrated bioprocess for culturing and manipulation of cartilaginous microtissues and anticipate the progressive substitution of manual operations with automated solutions for the manufacturing of microtissue-based living implants.
自动化技术在增强组织工程产品的稳健制造以实现临床转化方面具有吸引力。在这项工作中,我们提出了一种使用机器人平台进行媒体更换和软骨微组织在静态微井平台中培养的成像的自动化策略。我们使用自动化图像分析管道提取微组织位移和形态特征作为非侵入性质量属性。结果,空微井的识别准确率达到 96%,分割的骰子系数为 0.84。通过实验设计优化液体处理参数,以在长期分化方案中最小化空微井。我们发现,在手动速度及以上的抽吸或分配速度没有显著影响。相反,重复的媒体更换和培养时间是微组织位移的驱动力。由于绵羊模型是大型骨骼缺陷的临床前模型首选,我们使用羊骨膜来源的细胞形成软骨中间微组织。COL2A1 的表达增加证实了软骨分化,而 RUNX2 没有表现出成骨特异性。组织学分析显示较大的微组织中软骨细胞外基质和糖胺聚糖的分泌增加。此外,微组织植入物在裸鼠异位植入 4 周后能够形成矿化组织和骨。我们展示了用于培养和操作软骨微组织的集成生物工艺的开发,并期望随着自动化解决方案在制造基于微组织的活植入物方面的逐步取代,逐步取代手动操作。