Abu-Khader Ahmad, Pasha Roya, Ward Gwendoline C D, Boisjoli Gavin, Pineault Nicolas
Centre for Innovation, Canadian Blood Services, 1800 Alta Vista, Ottawa, ON, K1G 4J5, Canada.
Biochemistry, Microbiology and Immunology Department, University of Ottawa, Ottawa, Ottawa, ON, Canada.
Cytotechnology. 2016 Dec;68(6):2257-2269. doi: 10.1007/s10616-016-0019-6. Epub 2016 Oct 18.
Engraftment outcomes are strongly correlated with the numbers of hematopoietic stem and progenitor cells (HSPC) infused. Expansion of umbilical cord blood (CB) HSPC has gained much interest lately since infusion of expanded HSPC can accelerate engraftment and improve clinical outcomes. Many novel protocols based on different expansion strategies of HSPC and their downstream derivatives are under development. Herein, we describe the production and properties of serum-free medium (SFM) conditioned with mesenchymal stromal cells derived-osteoblasts (OCM) for the expansion of umbilical CB cells and progenitors. After optimization of the conditioning length, we show that OCM increased the production of human CB total nucleated cells and CD34 cells by 1.8-fold and 1.5-fold over standard SFM, respectively. Production of immature CD34 subpopulations enriched in hematopoietic stem cells was also improved with a shorter conditioning period. Moreover, we show that the growth modulatory activities of OCM on progenitor expansion are regulated by both soluble factors and non-soluble cellular elements. Finally, the growth and differentiation modulatory activities of OCM were fully retained after high dose-ionizing irradiation and highly stable when OCM is stored frozen. In summary, our results suggest that OCM efficiently mimics some of the natural regulatory activities of osteoblasts on HSPC and highlight the marked expansion potentials of SFM conditioned with osteoblasts.
植入结果与输注的造血干细胞和祖细胞(HSPC)数量密切相关。由于输注扩增后的HSPC可加速植入并改善临床结果,脐带血(CB)HSPC的扩增近来备受关注。许多基于HSPC及其下游衍生物不同扩增策略的新方案正在研发中。在此,我们描述了用间充质基质细胞来源的成骨细胞(OCM)条件培养的无血清培养基(SFM)用于扩增脐带血CB细胞和祖细胞的制备方法及特性。在优化条件培养时间后,我们发现与标准SFM相比,OCM分别使人类脐带血总核细胞和CD34细胞产量增加了1.8倍和1.5倍。在较短的条件培养期内,富含造血干细胞的未成熟CD34亚群的产量也有所提高。此外,我们表明OCM对祖细胞扩增的生长调节活性受可溶性因子和不可溶性细胞成分的共同调控。最后,OCM在高剂量电离辐射后仍能完全保留其生长和分化调节活性,并且在冷冻保存时具有高度稳定性。总之,我们的结果表明OCM有效地模拟了成骨细胞对HSPC的一些天然调节活性,并突出了成骨细胞条件培养的SFM显著的扩增潜力。