首页> 美国卫生研究院文献>Biotechnology Reports >Proliferation extent of CD34+ cells as a key parameter to maximize megakaryocytic differentiation of umbilical cord blood-derived hematopoietic stem/progenitor cells in a two-stage culture protocol
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Proliferation extent of CD34+ cells as a key parameter to maximize megakaryocytic differentiation of umbilical cord blood-derived hematopoietic stem/progenitor cells in a two-stage culture protocol

机译:CD34 +细胞的增殖程度是在两个阶段的培养方案中最大化脐血来源的造血干/祖细胞巨核细胞分化的关键参数

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摘要

Co-infusion of ex-vivo generated megakaryocytic progenitors with hematopoietic stem/progenitor cells (HSC/HPC) may contribute to a faster platelet recovery upon umbilical cord blood (UCB) transplantation. A two stage protocol containing cell expansion and megakaryocyte (Mk) differentiation was established using human UCB CD34+-enriched cells. The expansion stage used a pre-established protocol supported by a human bone marrow mesenchymal stem cells (MSC) feeder layer and the differentiation stage used TPO (100 ng/mL) and IL-3 (10 ng/mL). 18% of culture-derived Mks had higher DNA content (>4 N) and were able to produce platelet-like particles. The proliferation extent of CD34+ cells obtained in the expansion stage (FI-CD34+), rather than expansion duration, determined as a key parameter for efficient megakaryocytic differentiation. A maximum efficiency yield (EY) of 48 ± 7.7 Mks/input CD34+ cells was obtained for a FI-CD34+ of 17 ± 2.5, where a higher FI-CD34+ of 42 ± 13 resulted in a less efficient megakaryocytic differentiation (EY of 22 ± 6.7 and 19 ± 4.6 %CD41).
机译:离体产生的巨核细胞祖细胞与造血干/祖细胞(HSC / HPC)共同注入可能有助于脐带血(UCB)移植后更快的血小板恢复。利用富含人UCB CD34 + 的细胞建立了包含细胞扩增和巨核细胞(Mk)分化的两阶段方案。扩展阶段使用由人骨髓间充质干细胞(MSC)饲养层支持的预先建立的方案,分化阶段使用TPO(100ng / mL)和IL-3(10ng / mL)。来自培养物的Mks中有18%的DNA含量较高(> 4 N),并且能够产生血小板样颗粒。扩增阶段获得的CD34 + 细胞的增殖程度(FI-CD34 + )而不是扩增持续时间被确定为有效的巨核细胞分化的关键参数。 FI-CD34 + 为17±2.5时,获得的最大效率产量(EY)为48±7.7 Mks /输入CD34 + 细胞,其中FI-CD34较高 + 为42±13,导致巨核细胞分化效率较低(EY为22±6.7和19±4.6%CD41)。

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