Cytokine-dependent ex vivo expansion of early subsets of CD34+ cord blood myeloid progenitors is enhanced by cord blood plasma, but expansion of the more mature subsets of progenitors is favored.

Blood cells Pub Date : 1994-01-01
L Ruggieri, S Heimfeld, H E Broxmeyer
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引用次数: 0

Abstract

Expansion of stem/progenitor cells has important implications for transplantation. We recently reported that a factor or factors in cord blood (CB), but not adult peripheral blood (PB), plasma enhanced replating of granulocyte erythroid macrophage megakaryocyte colony-forming units (CFU-GEMM) progenitors, a measure of self-renewal capacity. In this context, we evaluated effects of CB plasma, in comparison with PB plasma and fetal bovine serum (FBS), on ex vivo expansion of CD34+ column-separated (72-98% CD34+) CB cells using stroma-free cultures in the absence and presence of either PIXY321 (a granulocyte-macrophage colony-stimulating factor/interleukin-3 [GM-CSF/IL-3] fusion protein), IL-3+IL-6+IL-1, or steel factor (SLF) -/+ PIXY. CB plasma, PB plasma, or FBS alone did not sustain cell numbers. Combinations of CB plasma +SLF+PIXY induced maximal cumulative nucleated cell expansion (1044-fold), which was greater than that of PB plasma plus cytokines (633-fold) and FBS plus cytokines (142-fold). Total CD34+ cells peaked by day 7 with 7-fold expansion in the presence of CB plasma+SLF+PIXY compared with PB plasma or FBS with these same cytokines (threefold each). By day 7, total CFU-GEMM production in the presence of either PIXY, SLF+PIXY, or IL-3+IL-6+IL-1 was greater with CB plasma (maximum 11.4-fold average increases) than with PB plasma (6.8-fold increase). These increases were greater than with FBS. However, PB plasma was at least as good as CB plasma for expansion of immature and mature subsets of CFU-GM. The frequency of progenitors decreased with time, and expansion was coupled with differentiation. Although the proliferative capacity of CFU-GEMM was maintained, the capacity of CFU-GEMM to be replated decreased after time in suspension culture, suggesting age-related commitment of cells. Moreover, with plasma +SLF+PIXY for 7 days, expansion of more mature CFU-GM (responsive to GM-CSF) was greater (16-146-fold with CB plasma and 31-208-fold with PB plasma) than immature CFU-GM (responsive to GM-CSF+SFL) (4- to 14-fold with CB plasma and 6- to 17-fold with PB plasma). The results suggest that CB plasma enhances expansion of CFU-GEMM to a greater extent than PB plasma or FBS, but expansion in these cultures favors more mature subsets of cells.

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细胞因子依赖性CD34+脐带血髓系祖细胞早期亚群的体外扩增可通过脐带血血浆增强,但更成熟的祖细胞亚群的体外扩增更受青睐。
干细胞/祖细胞的扩增对移植具有重要意义。我们最近报道了脐带血(CB)中的一个或多个因子,而不是成人外周血(PB)中的一个或多个因子,血浆增强了粒细胞、红细胞巨噬细胞、巨核细胞集落形成单位(CFU-GEMM)祖细胞的复制,这是一种自我更新能力的衡量标准。在这种情况下,我们评估了CB血浆与PB血浆和胎牛血清(FBS)相比,在没有和存在PIXY321(粒细胞-巨噬细胞集落刺激因子/白细胞介素-3 [GM-CSF/IL-3]融合蛋白)、IL-3+IL-6+IL-1或钢铁因子(SLF) -/+ PIXY的情况下,使用无基质培养对CD34+柱分离(72-98% CD34+) CB细胞的体外扩增的影响。CB血浆、PB血浆或FBS单独不能维持细胞数量。CB血浆+SLF+PIXY组合诱导最大的累积有核细胞扩增(1044倍),大于PB血浆+细胞因子(633倍)和FBS +细胞因子(142倍)。总CD34+细胞在第7天达到峰值,与含有相同细胞因子的PB血浆或FBS相比,CB血浆+SLF+PIXY存在的CD34+细胞扩增7倍(各3倍)。到第7天,在PIXY、SLF+PIXY或IL-3+IL-6+IL-1存在的情况下,CB血浆的CFU-GEMM总产量(最大平均增加11.4倍)高于PB血浆(增加6.8倍)。这些增加比FBS更大。然而,在CFU-GM未成熟亚群和成熟亚群的扩张方面,PB血浆至少与CB血浆一样好。祖细胞出现的频率随时间的延长而降低,细胞扩增与分化相结合。虽然CFU-GEMM的增殖能力得到了维持,但经过一段时间的悬浮培养后,CFU-GEMM的复制能力下降,提示细胞的年龄相关承诺。此外,血浆+SLF+PIXY治疗7天,较成熟的CFU-GM(对GM-CSF有反应)的扩张(CB血浆16-146倍,PB血浆31-208倍)比未成熟的CFU-GM(对GM-CSF+SFL有反应)(CB血浆4- 14倍,PB血浆6- 17倍)更大。结果表明,与PB血浆或FBS相比,CB血浆能更大程度地促进CFU-GEMM的扩增,但在这些培养中,扩增有利于更成熟的细胞亚群。
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Index Blood sampling and blood film preparation and examination Performing a blood count Morphology of blood cells Detecting erroneous blood counts
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