State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237, P. R. China.
Artif Cells Nanomed Biotechnol. 2013 Apr;41(2):98-102. doi: 10.3109/10731199.2012.712043. Epub 2012 Aug 14.
The mononuclear cells were cultivated in stirred flasks at different agitation speeds of 30 rpm, 45 rpm, 60 rpm and 80 rpm. At the agitation speed of 30 rpm, total cells achieved higher expansion folds and the CFC density increased. When at higher agitation speed of 60 rpm or 80 rpm, the number of cells dropped rapidly and characteristics of hematopoietic stem/progenitor cells (HSPCs) were not maintained. Moreover, the culture duration of 6-9 days was better for HSPCs ex vivo expansion. These data indicated that HSPCs should be cultured at relatively low agitation speed and for a short-term period when cultured in stirred suspension system.
将单核细胞在搅拌瓶中以 30rpm、45rpm、60rpm 和 80rpm 的不同搅拌速度进行培养。在 30rpm 的搅拌速度下,总细胞实现了更高的扩增倍数,集落形成细胞(CFC)密度增加。当搅拌速度提高到 60rpm 或 80rpm 时,细胞数量迅速下降,造血干/祖细胞(HSPCs)的特性无法维持。此外,HSPCs 体外扩增的最佳培养时间为 6-9 天。这些数据表明,在搅拌悬浮培养系统中培养 HSPCs 时,应选择相对较低的搅拌速度和较短的培养时间。