Murine long-term repopulating ability is compromised by ex vivo culture in serum-free medium despite preservation of committed progenitors.

M Sekhar, J M Yu, T Soma, C E Dunbar
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引用次数: 22

Abstract

Hematopoietic progenitor cells can be maintained and expanded ex vivo in standard or serum-free culture medium supplemented with a variety of stimulatory cytokines. The use of serum-free medium allows specification of reproducible and precise growth conditions optimal for various applications and is more acceptable from a safety and regulatory point of view. Human and murine committed progenitor cells have been shown to be equivalently ro better supported by serum-free culture conditions in the presence of multicytokine combinations, but there is little information on the effects of such culture conditions on repopulating stem cells. We used a murine competitive repopulation model to assess the effect of serum-free versus serum-containing ex vivo culture on long-term reconstituting cells. Despite equivalent numbers of committed CFU-C and day 12 CFU-S present after 4 days of culture of murine marrow in serum-free or serum-containing conditions in the presence of IL-3, IL-6, and SCF, long-term reconstituting activity was significantly impaired by serum-free culture. These findings may have important implications for transplantation and gene therapy applications.

尽管保留了承诺的祖细胞,但在无血清培养基中体外培养小鼠的长期繁殖能力受到损害。
造血祖细胞可以在补充多种刺激细胞因子的标准培养基或无血清培养基中维持和体外扩增。使用无血清培养基可以为各种应用提供可重复和精确的生长条件,从安全和监管的角度来看,这是更可接受的。研究表明,在多细胞因子组合存在的情况下,无血清培养条件下,人类和小鼠的祖细胞同样可以得到更好的支持,但关于这种培养条件对干细胞再生的影响的信息很少。我们使用小鼠竞争性繁殖模型来评估无血清和含血清离体培养对长期重建细胞的影响。尽管在无血清或含血清条件下,在存在IL-3、IL-6和SCF的情况下,小鼠骨髓培养4天后存在相同数量的固定CFU-C和第12天的CFU-S,但无血清培养显著损害了长期重建活性。这些发现可能对移植和基因治疗应用具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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