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Quantitative Analysis Reveals Expansion of Human Hematopoietic Repopulating Cells After Short-term Ex Vivo Culture

机译:定量分析揭示了短期离体培养后人类造血重建细胞的扩增。

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摘要

Ex vivo culture of human hematopoietic cells is a crucial component of many therapeutic applications. Although current culture conditions have been optimized using quantitative in vitro progenitor assays, knowledge of the conditions that permit maintenance of primitive human repopulating cells is lacking. We report that primitive human cells capable of repopulating nonobese diabetic (NOD)/severe combined immunodeficiency (SCID) mice (SCID-repopulating cells; SRC) can be maintained and/or modestly increased after culture of CD34+CD38 cord blood cells in serum-free conditions. Quantitative analysis demonstrated a 4- and 10-fold increase in the number of CD34+CD38 cells and colony-forming cells, respectively, as well as a 2- to 4-fold increase in SRC after 4 d of culture. However, after 9 d of culture, all SRC were lost, despite further increases in total cells, CFC content, and CD34+ cells. These studies indicate that caution must be exercised in extending the duration of ex vivo cultures used for transplantation, and demonstrate the importance of the SRC assay in the development of culture conditions that support primitive cells.
机译:人造血细胞的离体培养是许多治疗应用的关键组成部分。尽管目前的培养条件已经通过体外祖细胞定量分析进行了优化,但是对于允许维持原始人类再繁殖细胞的条件的知识却缺乏。我们报告说,在培养CD34 + 后,能够维持和/或适度增加能够再生非肥胖型糖尿病(NOD)/严重联合免疫缺陷(SCID)小鼠的原始人类细胞(SCID再生细胞; SRC)。无血清条件下的CD38 -脐血细胞。定量分析表明,CD34 + CD38 -细胞和集落形成细胞的数量分别增加了4倍和10倍,并且增加了2到4倍培养4 d后SRC增加两倍。然而,培养9天后,尽管总细胞,CFC含量和CD34 + 细胞进一步增加,但所有SRC都丢失了。这些研究表明,在延长用于移植的离体培养的持续时间时必须谨慎行事,并证明SRC分析在支持原始细胞的培养条件发展中的重要性。

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