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哺乳动物细胞系在 100 毫升冷冻袋中冷冻保存的细胞库参数的表征。

Characterization of cell-banking parameters for the cryopreservation of mammalian cell lines in 100-mL cryobags.

机构信息

Cell Culture Development, Global Biological Development, Bayer HealthCare LLC, 800 Dwight Way, Berkeley, CA 94701, USA.

出版信息

Biotechnol Prog. 2010 Jul-Aug;26(4):1154-63. doi: 10.1002/btpr.427.

Abstract

This article describes a cell banking process for rBHK cell lines in 100-mL cryobags. As the use of larger volume cell banks requires greater cell numbers and longer preparation time, extensive characterization of key process parameters beyond the conventional ranges was performed to support a cGMP banking process. All experiments were conducted using two recombinant BHK21 cell lines, one of them cotransfected with Hsp70. The results show that the entire cell banking process for these BHK cell lines can be performed at room temperature. A DMSO exposure time up to 5 h either directly in a bioreactor or in shaker flasks did not result in any significant negative effect after cell thaw, when the cryocontainers were frozen immediately after filling. Extensive characterization did not indicate any significant apoptotic effects after thaw. However, the Hsp70 cotransfected cell line did show a slightly better protection from potential cryopreservation-induced apoptosis. Surprisingly, it was found that cells transferred into cryobags showed a low recovery rate after thaw if the incubation time exceeded 1.5 h before freezing. Additional experiments confirmed that the DMSO exposure time inside the cryocontainer in contrast to the DMSO exposure in a reactor or shaker flasks is much more critical. The cryobag cell banking process should therefore be performed within a 1(1/2)-2 h window; a banking process for vials should not exceed 2(1/2) h.

摘要

本文介绍了在 100 毫升冷冻袋中进行 rBHK 细胞系细胞库的过程。由于使用更大体积的细胞库需要更多的细胞数量和更长的准备时间,因此对关键工艺参数进行了广泛的特征描述,超出了传统范围,以支持 cGMP 银行处理。所有实验均使用两种重组 BHK21 细胞系进行,其中一种与 Hsp70 共转染。结果表明,这些 BHK 细胞系的整个细胞库过程可以在室温下进行。直接在生物反应器或摇瓶中进行长达 5 小时的 DMSO 暴露,在填充后立即冷冻冷冻容器时,解冻后不会产生任何显着的负面影响。广泛的特征描述表明解冻后没有明显的凋亡作用。然而,Hsp70 共转染的细胞系确实显示出对潜在冷冻保存诱导的凋亡的稍好保护作用。令人惊讶的是,发现如果在冷冻之前的孵育时间超过 1.5 小时,转移到冷冻袋中的细胞在解冻后恢复率较低。额外的实验证实,与在反应器或摇瓶中的 DMSO 暴露相比,冷冻容器内的 DMSO 暴露时间更为关键。因此,冷冻袋细胞库处理应在 1(1/2)-2 小时的窗口内进行;小瓶的银行处理不应超过 2(1/2)小时。

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