Development of three-dimensional cell culture bioprocesses

三维细胞培养生物过程的开发

• 批准号: RGPIN-2015-06271
• 负责人: Hoesli, Corinne
• 金额: $ 1.82万
• 依托单位: McGill University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2019
• 资助国家: 加拿大
• 起止时间: 2019-01-01 至 2020-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=680517
• 关键词: Development; three; dimensional; cell; culture

Applications of immobilized cell culture range from the stabilization of probiotic bacteria to tissue engineering and cellular therapy. The 3D organisation of the cells within the materials affects nutrient and waste product concentration gradients, and hence product performance. In addition, manufacturing complex 3D constructs while optimizing both cellular function and material properties is currently challenging. The long-term goal of the proposed research program is to develop bioprocesses to scale up the production of cells in complex 3D environments. The 5-year goal of this program is to develop methods to encapsulate pancreatic cell clusters in hydrogel beads such as alginate beads. Alginate is a negatively charged linear polysaccharide used in clinical trials of encapsulated pancreatic islet transplantation to treat diabetes, and is broadly used in several other cellular therapy applications. Alginate emulsification and internal gelation is a simple and robust alginate bead production method that I have previously adapted to mammalian cell immobilisation. The process is highly scaleable, but produces beads with a broad bead size distribution, which leads to between-bead differences in mechanical properties and performance. So far, the optimisation of cell survival and bead properties as a function of process parameters has relied mainly on empirical observations. To obtain monodisperse beads with well-controlled mechanical properties and effects on the encapsulated cells, the proposed approach is to develop a novel microchannel emulsification-based cell encapsulation process. The short-term objectives are to (1) model hydrogel bead formation kinetics, (2) develop and (3) optimise a microchannel emulsification-based process for cell encapsulation, and then (4) test the effect of the resulting bead properties on pancreatic cell function. These novel cell immobilisation strategies represent a significant advance towards scaleable three-dimensional cell culture in hydrogels with well-controlled physical properties. These novel bioprocesses could be applied to other cell types that require three-dimensional scaffolds to maximize desired biological functions. This research program addresses key limitations of cell immobilisation bioprocesses.

固定细胞培养的应用范围从益生菌的稳定到组织工程和细胞治疗。材料中细胞的3D组织会影响养分和废物产物浓度梯度，从而影响产品性能。此外，在优化细胞功能和材料特性的同时，制造复合体3D构建体具有挑战性。拟议的研究计划的长期目标是开发生物过程，以扩大复杂3D环境中细胞的生产。该程序的5年目标是开发将胰凝胶珠（如藻酸珠）中封装胰腺细胞簇的方法。藻酸盐是一种负电荷的线性多糖，用于封装的胰岛移植以治疗糖尿病，并广泛用于其他几种细胞治疗应用中。藻酸盐乳化和内部凝胶化是一种简单且坚固的藻酸盐珠的产生方法，我以前已适应哺乳动物细胞固定。该过程是高度可扩展的，但是产生具有宽珠尺寸分布的珠子，从而导致机械性能和性能之间的差异差异。到目前为止，细胞存活和珠子性能作为过程参数的函数的优化主要依赖于经验观察。为了获得具有良好控制的机械性能以及对封装细胞的影响的单分散珠，建议的方法是开发一种新型的基于微通道乳化的细胞包封过程。短期目标是（1）模型水凝胶珠的形成动力学，（2）开发和（3）优化基于微通道的基于微通道的乳化过程，然后（4）（4）测试所得的珠子性能对胰腺细胞功能的影响。这些新型的细胞固定策略代表了具有良好控制的物理特性的水凝胶中可扩展的三维细胞培养的重大进展。这些新型的生物处理可以应用于需要三维支架以最大化所需生物学功能的其他细胞类型。该研究计划解决了细胞固定生物过程的关键局限性。