Uncoupling of cell growth and proliferation results in enhancement of productivity in p21C1P1-arrested CHO cells

被引:98
作者
Bi, JX
Shuttleworth, J
Ai-Rubeai, M [1 ]
机构
[1] Univ Birmingham, Dept Chem Engn, Birmingham B15 2TT, W Midlands, England
[2] Univ Birmingham, Sch Med, Birmingham B15 2TT, W Midlands, England
关键词
cyclin-dependent kinase; cell cycle arrest; growth control; metabolic engineering;
D O I
10.1002/bit.20025
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chinese hamster ovary cells have c been engineered to inducibly over-express the p21(CIP1) cyclin-dependent kinase inhibitor, to achieve cell cycle arrest and increase cell productivity. In p21(CIP1)-arrested cells production of antibody from a stably integrated IgG4 gene, was enhanced approximately fourfold. The underlying physiological basis for enhanced productivity was investigated by measuring a range of cellular and metabolic parameters. Interestingly, the average cell volume of arrested cells was approximately fourfold greater than that of proliferating cells. This was accompanied by significant increases in mitochondrial mass, mitochondrial activity, and ribosomal protein S6 levels. Our results suggest that p21(CIP1)-induced cell cycle arrest uncouples cell growth from cell-cycle progression, and provides new insight into how improved productivity can be achieved in a cell line commonly used for large-scale production of pharmaceutical proteins. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:741 / 749
页数:9
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