在多室生物反应器中利用胶原-黄芪支架从脐带血干细胞高效生产血小板

Mohamad Hosein Derakhti Gonbad, A. Khoshfetrat, Akbar Movassaghpuor, Z. Sanaat, H. N. Charoudeh
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引用次数: 0

摘要

背景:迄今为止,血小板(PLT)输血是治疗血小板减少症的主要医学选择。如今,同种异体造血干细胞被广泛用于献血。由于制备和储存plt的局限性,研究人员试图开发替代模式,如生物反应器,通过促进不同类型的干细胞分化为巨核细胞(MK)和plt,用于体外扩增和生产用于治疗目的的plt。材料与方法:本实验研究将脐带血干细胞(UCB-SC)分化为MK。为此,开发了一种新的生物反应器系统,该系统由六个隔间和胶原蛋白和天然黄棘胶制成的双层支架组成,以模拟骨髓样结构。将mk加载到支架顶层后,分析剪切应力作用下plt的生成速率。结果:根据估计,每个MK产生约17.42个plt装载到支架胶原中。胶原-黄软骨支架组和纯黄软骨支架组的plt分别为23.46和9.44,胶原-黄软骨支架中plt的增加有统计学意义(p < 0.001)。生成的plt在总体上有积极的反应,并与正常的plt相互作用。结论:综上所述,设计的生物反应器与胶原-黄棘底物可以用于生产足够数量的临床用途的plt。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient Production of Platelets from Umbilical Cord Blood Stem Cells Using A Collagen-Tragacanth Scaffold in A Multi-Chamber Bioreactor
Background: To date, platelet (PLT) transfusion is the main medical option for the treatment of thrombocytopenia. Nowadays, allogenic PLTs are commonly used for blood donation. Due to the limitations in the preparation and storage of PLTs, researchers try to develop alternative modalities such as bioreactors for the in-vitro expansion and production of PLTs for therapeutic purposes by promoting the differentiation of different types of stem cells into megakaryocytes (MK) and PLTs. Materials and Methods: In this experimental study, umbilical cord blood stem cells (UCB-SC) were differentiated into MK. To this end, a new bioreactor system consisting of six compartments and a two-layer scaffold made of collagen and natural tragacanth gum was developed to mimic a bone marrow-like structure. After MKs were loaded to the top layer of the scaffold, the production rate of PLTs was analyzed under shear stress. Results: Based on the estimation, each MK produced about 17.42 PLTs loaded into the scaffold collagen. This value emerged to be 23.46 and 9.44 PLTs in the collagen-tragacanth and the pure tragacanth scaffold groups, respectively, the increase of PLTs in the collagen-tragacanth scaffold was statistically significant (p < 0.001).The generated PLTs had a positive response in aggregometry as well as interaction with normal PLTs. Conclusion: Taken together, the designed bioreactor with a collagen-tragacanth substrate can be used for the production of a sufficient number of PLTs for clinical purposes.
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