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High density cultivation of genetically-engineered CHO cell lines with microcarrier culture systems.

作者信息

Xiao C, Huang Z, Liu F, Guo Z, Gao L

机构信息

Institute of Biotechnology, Academy of Military Medical Sciences, Beijing.

出版信息

Chin Med Sci J. 1994 Jun;9(2):71-4.

PMID:8000063
Abstract

Genetically-engineered CHO cell lines, r beta-13 and CLF-8B2, were cultivated with the MC-1 microcarrier culture system. The cell density could be enhanced by increasing the concentration of microcarrier. At a microcarrier concentration of 10 mg/ml, the cell density could reach 4 to 5 x 10(6) cells/ml. It was shown that these cell lines would spontaneously release from the microcarrier to attach to and proliferate on fresh microcarriers. We were thus able to scale up cultivation using a simple method, i.e. by adding fresh microcarriers and medium directly into the culture system to about 2, 4 or 8 times the original volume. Using a perfusion culture system, we have successfully cultivated CLF-8B2 cells in a 2 L bioreactor for several weeks at medium perfusion rates of 0.5 to 3 working volumes. Prourokinase was stably secreted.

摘要

相似文献

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引用本文的文献

1
High density and scale-up cultivation of recombinant CHO cell line and hybridomas with porous microcarrier Cytopore.高密度和规模化培养重组 CHO 细胞系和杂交瘤细胞与多孔微载体 Cytopore。
Cytotechnology. 1999 Jul;30(1-3):143-7. doi: 10.1023/A:1008038609967.
2
Pilot production of u-PA with porous microcarrier cell culture.多孔微载体细胞培养法生产 u-PA 的中试生产。
Cytotechnology. 2000 Jul;33(1-3):13-9. doi: 10.1023/A:1008127310890.