减少氧化应激可改善基于聚合物的体外人类造血干细胞和祖细胞培养及基因编辑效果

Yavor Bozhilov, Elizabeth Brown, Ian Hsu, Indranil Singh, Alejo Rodriguez-Fraticelli, Anindita Roy, Satoshi Yamazaki, Adam C Wilkinson
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引用次数: 0

摘要

自我更新的多能造血干细胞(造血干细胞)具有独特的能力,可在移植后稳定地再生整个血液和免疫系统。在临床上,造血干细胞被用于为各种血液病患者重建健康的血液系统。然而,造血干细胞非常稀少,体内外培养也很困难,这阻碍了为基础研究和临床治疗收集大量造血干细胞的努力。最近开发了基于聚合物的培养条件,以支持小鼠和人类造血干细胞和祖细胞(HSPCs)的扩增。小鼠造血干细胞在聚合物培养基中迅速扩增,而人类造血干细胞在聚合物培养基中的生长速度却被限制在4周内增长约70倍。在这里,我们发现减少氧化应激可改善人类 HSPC 在这些条件下的生长。我们描述了一种优化的培养条件,通过降低氧张力和添加抗氧化剂,可在4周内将生长速度提高250-1400倍。这些条件还能在这些基于聚合物的培养物中实现高效的基因编辑。我们设想,这些改进的培养条件将支持人类 HSPC 生物学的一系列研究,并为临床规模的 HSPC 扩增和基因编辑提供一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reducing oxidative stress improves ex vivo polymer-based human haematopoietic stem and progenitor cell culture and gene editing
Self-renewing multipotent haematopoietic stem cells (HSCs) have the unique capacity to stably regenerate the entire blood and immune systems following transplantation. HSCs are used clinically to reconstitute a healthy blood system in patients suffering from a range of haematological diseases. However, HSCs are very rare and have been challenging to grow ex vivo, which has hampered efforts to collect large numbers of HSCs for both basic research and clinical therapies. Polymer-based culture conditions have recently been developed to support expansion of mouse and human haematopoietic stem and progenitor cells (HSPCs). While mouse HSPCs expanded rapidly in polymer-based cultures, growth speeds for human HSPCs in polymer-based cultures was limited to ~70-fold over 4-weeks. Here we have found that reducing oxidative stress improves human HSPC growth in these conditions. We describe an optimised culture condition that improves growth to 250-1400-fold over 4-weeks through reducing oxygen tension and the addition of antioxidants. These conditions also enable efficient gene editing in these polymer-based cultures. We envision these improved culture conditions will support a range of research into human HSPC biology and provide a platform for clinical-scale HSPC expansion and gene editing.
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