细胞因子对不同人造血干细胞体外扩增的影响。

S Eridani, U Mazza, P Massaro, M L La Targia, A T Maiolo, A Mosca
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引用次数: 14

摘要

人类多能干细胞(PSC)是目前移植尝试和基因操作的目标。因此,我们研究了不同类型血液样本中PSC的频率和扩增潜力。因此,从人骨髓(BM)、外周血(PB)和脐带血(CB)样本中获得了cd34 +细胞。经免疫磁分离后,BM(1.08 ~ 2.25%)和CB(0.42 ~ 1.32%)的cd34 +细胞产率最高,PB的产率较低。然后在造血生长因子组合存在的情况下,建立三种来源的PSC悬浮培养。有核细胞池的扩增在培养10 ~ 15天达到最大值;当向培养基中添加促红细胞生成素(Epo)时,可实现最早和最大的扩增(高达220倍),但这导致集落形成细胞减少并分化为红系祖细胞。BFU-E衍生菌落的克隆性试验显示,液体培养第5天达到峰值。进一步的研究是可取的,以确定最佳的细胞因子组合,以获得有价值的体外扩增,同时保存干细胞特性。
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Cytokine effect on ex vivo expansion of haemopoietic stem cells from different human sources.

Human pluripotential stem cells (PSC) are currently the target for transplantation attempts and genetic manipulation. We have therefore investigated the frequency and the expansion potential of PSC's in different types of blood samples. CD 34+ cells were thus obtained from human bone marrow (BM), as well as from peripheral blood (PB) and cord blood (CB) samples. After immuno-magnetic separation the highest yields of CD 34+ cells were from BM (1.08-2.25%) and CB (0.42-1.32%) while PB samples gave much lower values. Suspension cultures of PSC's from the three sources were then set up, in the presence of combinations of haemopoietic growth factors. A remarkable amplification of the nucleated cell pool was observed reaching a maximum between 10 and 15 days of culture; earliest and maximum expansion (up to 220-fold) was achieved when Erythropoietin (Epo) was added to the culture medium, but this resulted in reduction of colony-forming cells and differentiation into erythroid progenitors. Clonogenic tests for BFU-E's derived colonies showed a peak value at 5 days of liquid culture. Further studies are advisable to establish the best cytokine combination for a valuable ex vivo expansion, coupled with preservation of stem cell properties.

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