用于骨骼组织工程应用的机器人驱动的软骨微组织制造。

IF 5.4 2区 医学 Q1 CELL & TISSUE ENGINEERING
Isaak Decoene, Gabriele Nasello, Rodrigo Furtado Madeiro de Costa, Gabriella Nilsson Hall, Angela Pastore, Inge Van Hoven, Samuel Ribeiro Viseu, Catherine Verfaillie, Liesbet Geris, Frank P Luyten, Ioannis Papantoniou
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引用次数: 0

摘要

自动化技术对于提高组织工程产品的稳健生产和临床转化具有吸引力。在这项工作中,我们提出了一种自动化策略,利用机器人平台对静态微孔平台中培养的软骨微组织进行培养基更换和成像。我们使用自动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,空微细胞的识别准确率达到 96%,分割的骰子系数为 0.84。实验设计用于优化液体处理参数,以尽量减少长期分化方案中的空微孔。我们发现,在手动速度和手动速度之外,吸液或分散速度没有明显影响。相反,反复更换培养基和培养时间是微组织位移的驱动力。由于绵羊模型是大面积骨骼缺损的临床前首选模型,我们使用绵羊骨膜衍生细胞来形成软骨中间微组织。COL2A1的表达增加证实了软骨分化,而RUNX2则显示没有成骨规格。组织学分析表明,在较大的微组织中,软骨细胞外基质和糖胺聚糖的分泌量增加。此外,基于微组织的植入物在裸鼠体内异位植入 4 周后,能够形成矿化组织和骨骼。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过程,并预计在制造基于微组织的活体植入物时,自动化解决方案将逐步取代人工操作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Robotics-Driven Manufacturing of Cartilaginous Microtissues for Skeletal Tissue Engineering Applications.

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.

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来源期刊
Stem Cells Translational Medicine
Stem Cells Translational Medicine CELL & TISSUE ENGINEERING-
CiteScore
12.90
自引率
3.30%
发文量
140
审稿时长
6-12 weeks
期刊介绍: STEM CELLS Translational Medicine is a monthly, peer-reviewed, largely online, open access journal. STEM CELLS Translational Medicine works to advance the utilization of cells for clinical therapy. By bridging stem cell molecular and biological research and helping speed translations of emerging lab discoveries into clinical trials, STEM CELLS Translational Medicine will help move applications of these critical investigations closer to accepted best patient practices and ultimately improve outcomes. The journal encourages original research articles and concise reviews describing laboratory investigations of stem cells, including their characterization and manipulation, and the translation of their clinical aspects of from the bench to patient care. STEM CELLS Translational Medicine covers all aspects of translational cell studies, including bench research, first-in-human case studies, and relevant clinical trials.
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