CHO cells in biotechnology for production of recombinant proteins: current state and further potential

被引:535
作者
Kim, Jee Yon [1 ]
Kim, Yeon-Gu [2 ]
Lee, Gyun Min [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Grad Sch Nanosci & Technol WCU, Dept Biol Sci, Taejon 305701, South Korea
[2] KRIBB, Ctr Biotechnol Proc Engn, Taejon 305806, South Korea
基金
新加坡国家研究基金会;
关键词
CHO cells; Cell line development; Vector engineering; Cell engineering; Omics-based approaches; CHINESE-HAMSTER OVARY; BUTYRATE-INDUCED APOPTOSIS; GENE INTEGRATION SYSTEM; LOW CULTURE TEMPERATURE; HUMAN ANTITHROMBIN-III; LACTIC-ACID FORMATION; SERUM-FREE; DISULFIDE-ISOMERASE; THROMBOPOIETIN PRODUCTIVITY; CONTROLLED PROLIFERATION;
D O I
10.1007/s00253-011-3758-5
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
Recombinant Chinese hamster ovary cells (rCHO) cells have been the most commonly used mammalian host for large-scale commercial production of therapeutic proteins. Recent advances in cell culture technology for rCHO cells have achieved significant improvement in protein production leading to titer of more than 10 g/L to meet the huge demand from market needs. This achievement is associated with progression in the establishment of high and stable producer and the optimization of culture process including media development. In this review article, we focus on current strategies and achievements in cell line development, mainly in vector engineering and cell engineering, for high and stable protein production in rCHO cells. The approaches that manipulate various DNA elements for gene targeting by site-specific integration and cis-acting elements to augment and stabilize gene expression are reviewed here. The genetic modulation strategy by "direct" cell engineering with growth-promoting and/or productivity-enhancing factors and omics-based approaches involved in transcriptomics, proteomics, and metabolomics to pursue cell engineering are also presented.
引用
收藏
页码:917 / 930
页数:14
相关论文
共 135 条
[1]   Life-or-death decisions by the Bcl-2 protein family [J].
Adams, JM ;
Cory, S .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (01) :61-66
[2]   Life and death in mammalian cell culture: strategies for apoptosis inhibition [J].
Arden, N ;
Betenbaugh, MJ .
TRENDS IN BIOTECHNOLOGY, 2004, 22 (04) :174-180
[3]   Inhibiting the apoptosis pathway using MDM2 in mammalian cell cultures [J].
Arden, Nilou ;
Majors, Brian S. ;
Ahn, Shin-Hyung ;
Oyler, George ;
Betenbaugh, Michael J. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 97 (03) :601-614
[4]   The role of Bcl-2 and its combined effect with p21CIP1 in adaptation of CHO cells to suspension and protein-free culture [J].
Astley, Kelly ;
Al-Rubeai, Mohamed .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2008, 78 (03) :391-399
[5]   Limitations to the comparative proteomic analysis of thrombopoietin producing Chinese hamster ovary cells treated with sodium butyrate [J].
Baik, Jong Youn ;
Joo, Eun Jin ;
Kim, Young Hwan ;
Lee, Gyun Min .
JOURNAL OF BIOTECHNOLOGY, 2008, 133 (04) :461-468
[6]   Proteomic understanding of intracellular responses of recombinant chinese hamster ovary cells adapted to grow in serum-free suspension culture [J].
Baik, Jong Youn ;
Ha, Tae Kwang ;
Kim, Young Hwan ;
Lee, Gyun Min .
BIOTECHNOLOGY PROGRESS, 2011, 27 (06) :1680-1688
[7]   A DIGE Approach for the Assessment of Differential Expression of the CHO Proteome Under Sodium Butyrate Addition: Effect of Bcl-xL Overexpression [J].
Baik, Jong Youn ;
Lee, Gyun Min .
BIOTECHNOLOGY AND BIOENGINEERING, 2010, 105 (02) :358-367
[8]   Initial transcriptome and proteome analyses of low culture temperature-induced expression in CHO cells producing erythropoietin [J].
Baik, JY ;
Lee, MS ;
An, SR ;
Yoon, SK ;
Joo, EJ ;
Kim, YH ;
Park, HW ;
Lee, GM .
BIOTECHNOLOGY AND BIOENGINEERING, 2006, 93 (02) :361-371
[9]   Stability of protein production from recombinant mammalian cells [J].
Barnes, LM ;
Bentley, CM ;
Dickson, AJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2003, 81 (06) :631-639
[10]   Engineering CHO cell growth and recombinant protein productivity by overexpression of miR-7 [J].
Barron, N. ;
Kumar, N. ;
Sanchez, N. ;
Doolan, P. ;
Clarke, C. ;
Meleady, P. ;
O'Sullivan, F. ;
Clynes, M. .
JOURNAL OF BIOTECHNOLOGY, 2011, 151 (02) :204-211