Department of Applied Bioscience, CHA University, Seoul, 135-081, Korea.
Biotechnol Lett. 2010 Dec;32(12):1969-75. doi: 10.1007/s10529-010-0355-0. Epub 2010 Jul 22.
For the ex vivo expansion of CD34(+) cells, culture conditions were optimized using cytokine cocktails and media change methods. In addition, static, orbital-shake, and stirred cultures were compared. After cultivation, total cell expansion, immunophenotypes, clonogenic ability, and metabolite concentration in media were analyzed. Optimized media change methods enhanced the number of total nucleated cells (TNCs) by 600-fold (from 10(4) to 6 × 10(6) cells) in static cultures. Furthermore, intermittent orbital-shake cultures gave the highest fold increase of TNCs and CD34(+)/CD38(-) cells. These results imply that proliferation of CD34(+) cells in intermittent shake cultures was more efficient than that in static cultures under optimized culture conditions.
为了体外扩增 CD34(+)细胞,使用细胞因子鸡尾酒和培养基更换方法优化了培养条件。此外,还比较了静态、轨道摇晃和搅拌培养。培养后,分析了总细胞扩增、免疫表型、集落形成能力和培养基中代谢物浓度。优化的培养基更换方法使静态培养中的总核细胞(TNC)数量增加了 600 倍(从 10(4)到 6 × 10(6)个细胞)。此外,间歇性轨道摇晃培养使 TNC 和 CD34(+) / CD38(-)细胞的倍增倍数最高。这些结果表明,在优化的培养条件下,CD34(+)细胞在间歇摇床培养中的增殖效率高于静态培养。