首页> 美国卫生研究院文献>Tissue Engineering. Part C Methods >Compartmental Hollow Fiber Capillary Membrane–Based Bioreactor Technology for In Vitro Studies on Red Blood Cell Lineage Direction of Hematopoietic Stem Cells
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Compartmental Hollow Fiber Capillary Membrane–Based Bioreactor Technology for In Vitro Studies on Red Blood Cell Lineage Direction of Hematopoietic Stem Cells

机译:基于隔室空心纤维毛细管膜的生物反应器技术对造血干细胞红细胞谱系方向的体外研究

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摘要

Continuous production of red blood cells (RBCs) in an automated closed culture system using hematopoietic stem cell (HSC) progenitor cell populations is of interest for clinical application because of the high demand for blood transfusions. Previously, we introduced a four-compartment bioreactor that consisted of two bundles of hollow fiber microfiltration membranes for transport of culture medium (forming two medium compartments), interwoven with one bundle of hollow fiber membranes for transport of oxygen (O2), carbon dioxide (CO2), and other gases (forming one gas compartment). Small-scale prototypes were developed of the three-dimensional (3D) perfusion cell culture systems, which enable convection-based mass transfer and integral oxygenation in the cell compartment. CD34+ HSC were isolated from human cord blood units using a magnetic separation procedure. Cells were inoculated into 2- or 8-mL scaled-down versions of the previously designed 800-mL cell compartment devices and perfused with erythrocyte proliferation and differentiation medium. First, using the small-scale 2-mL analytical scale bioreactor, with an initial seeding density of 800,000 cells/mL, we demonstrated approximately 100-fold cell expansion and differentiation after 7 days of culture. An 8-mL laboratory-scale bioreactor was then used to show pseudocontinuous production by intermediately harvesting cells. Subsequently, we were able to use a model to demonstrate semicontinuous production with up to 14,288-fold expansion using seeding densities of 800,000 cells/mL. The down-scaled culture technology allows for expansion of CD34+ cells and stimulating these progenitors towards RBC lineage, expressing approximately 40% CD235+ and enucleation. The 3D perfusion technology provides an innovative tool for studies on RBC production, which is scalable.
机译:由于对输血的高需求,使用造血干细胞(HSC)祖细胞群体在自动封闭培养系统中连续生产红细胞(RBC)引起了临床应用的兴趣。之前,我们介绍了一种四室生物反应器,该反应器由两束中空纤维微滤膜组成,用于运输培养基(形成两个介质室),并与一束中空纤维膜交织,用于运输氧气(O2),二氧化碳( CO2)和其他气体(形成一个气体室)。开发了三维(3D)灌注细胞培养系统的小规模原型,该系统可实现基于对流的传质和细胞室内的整体充氧。使用磁分离程序从人脐血单位中分离出CD34 + HSC。将细胞接种到先前设计的800mL细胞隔室装置的2-mL或8-mL缩小版本中,并灌注红细胞增殖和分化培养基。首先,使用小规模的2-mL分析规模的生物反应器,初始接种密度为800,000个细胞/ mL,我们在培养7天后证明了约100倍的细胞扩增和分化。然后使用8 mL实验室规模的生物反应器通过中间收获细胞显示伪连续生产。随后,我们能够使用一个模型来演示半连续生产,并使用800,000个细胞/ mL的接种密度进行多达14288倍的扩增。规模缩小的培养技术可扩增CD34 + 细胞,并刺激这些祖细胞趋向RBC谱系,表达约40%CD235 + 和去核。 3D灌注技术为可扩展的RBC生产研究提供了创新工具。

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