Cambridge Centre for Medical Materials, Department of Materials Science and Metallurgy, 27 Charles Babbage Road, Cambridge CB3 0FS, UK.
Department of Haematology, University of Cambridge, National Health Blood Service Centre, Long Road, Cambridge CB2 0PT, UK.
Biomaterials. 2018 Nov;182:135-144. doi: 10.1016/j.biomaterials.2018.08.019. Epub 2018 Aug 8.
Platelet transfusions are a key treatment option for a range of life threatening conditions including cancer, chemotherapy and surgery. Efficient ex vivo systems to generate donor independent platelets in clinically relevant numbers could provide a useful substitute. Large quantities of megakaryocytes (MKs) can be produced from human pluripotent stem cells, but in 2D culture the ratio of platelets harvested from MK cells has been limited and restricts production rate. The development of biomaterial cell supports that replicate vital hematopoietic micro-environment cues are one strategy that may increase in vitro platelet production rates from iPS derived Megakaryocyte cells. In this paper, we present the results obtained generating, simulating and using a novel structurally-graded collagen scaffold within a flow bioreactor system seeded with programmed stem cells. Theoretical analysis of porosity using micro-computed tomography analysis and synthetic micro-particle filtration provided a predictive tool to tailor cell distribution throughout the material. When used with MK programmed stem cells the graded scaffolds influenced cell location while maintaining the ability to continuously release metabolically active CD41 CD42 functional platelets. This scaffold design and novel fabrication technique offers a significant advance in understanding the influence of scaffold architectures on cell seeding, retention and platelet production.
血小板输注是治疗包括癌症、化疗和手术在内的多种危及生命疾病的关键治疗选择。有效的体外系统可以生成供体独立的血小板,数量在临床相关范围内,这可能是一种有用的替代方法。大量巨核细胞(MK)可以从人类多能干细胞中产生,但在二维培养中,从 MK 细胞中收获的血小板的比例受到限制,从而限制了产量。复制重要造血微环境线索的生物材料细胞支持物是一种可能提高 iPS 衍生巨核细胞系体外血小板产量的策略。在本文中,我们介绍了在流式生物反应器系统中使用新型结构梯度胶原支架生成、模拟和使用可编程干细胞的结果。使用微计算机断层扫描分析和合成微颗粒过滤对孔隙率进行理论分析,提供了一种可预测的工具,用于调整细胞在整个材料中的分布。当与 MK 编程干细胞一起使用时,梯度支架影响细胞位置,同时保持持续释放代谢活跃的 CD41 CD42 功能性血小板的能力。这种支架设计和新型制造技术在理解支架结构对细胞接种、保留和血小板生成的影响方面取得了重大进展。