Isolation, characterization and recombinant protein expression in Veggie-CHO: A serum-free CHO host cell line

被引:36
作者
Rasmussen, B [1 ]
Davis, R [1 ]
Thomas, J [1 ]
Reddy, P [1 ]
机构
[1] Immunex Corp, Dept Cell Sci, Seattle, WA 98101 USA
关键词
CHO; DHFR; gene expression; growth factor; recombinant protein; serum-free;
D O I
10.1023/A:1008052908496
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
The dihydrofolate reductase-deficient Chinese hamster ovary cell line, DXB11-CHO, commonly used as a host cell for the production of recombinant proteins requires 7.5% serum-supplementation for optimal growth. Regulatory issues surrounding the use of serum in clinical production processes and the direct and indirect costs of using serum in large-scale production and recovery processes have triggered efforts to derive serum-independent host cell lines. We have successfully isolated a serum-free host that we named Veggie-CHO. Veggie-CHO was generated by adapting DXB11-CHO cells to growth in serum-free media in the absence of exogenous growth factors such as Transferrin and Insulin-like growth factor, which we have previously shown to be essential for growth and viability of DXB11-CHO cells. Veggie-CHO cells have been shown to maintain an average doubling time of 22 hr in continuous growth cultures over a period of three months and have retained the dihydrofolate reductase -deficient phenotype of their parental DXB11-CHO cells. These properties and the stability of its serum-free phenotype have allowed the use of Veggie-CHO as host cells for transfection and amplified expression of recombinant proteins. We describe the derivation a serum-free recombinant cell line with an average doubling time of 20 hr and specific productivity of 2.5 Units recombinant Flt-3L protein per 10e6 cells per day.
引用
收藏
页码:31 / 42
页数:12
相关论文
共 26 条
[1]   DESIGN AND OPERATION OF A RECOMBINANT MAMMALIAN-CELL MANUFACTURING PROCESS FOR RFVIII [J].
ADAMSON, R .
ANNALS OF HEMATOLOGY, 1994, 68 :S9-S14
[2]   METHODS FOR GROWTH OF CULTURED-CELLS IN SERUM-FREE MEDIUM [J].
BARNES, D ;
SATO, G .
ANALYTICAL BIOCHEMISTRY, 1980, 102 (02) :255-270
[3]   EFFECT OF TEMPERATURE ON HYBRIDOMA CELL-CYCLE AND MAB PRODUCTION [J].
BLOEMKOLK, JW ;
GRAY, MR ;
MERCHANT, F ;
MOSMANN, TR .
BIOTECHNOLOGY AND BIOENGINEERING, 1992, 40 (03) :427-431
[4]   Hematologic effects of flt3 ligand in vivo in mice [J].
Brasel, K ;
McKenna, HJ ;
Morrissey, PJ ;
Charrier, K ;
Morris, AE ;
Lee, CC ;
Williams, DE ;
Lyman, SD .
BLOOD, 1996, 88 (06) :2004-2012
[5]   Reactivation of silenced, virally transduced genes by inhibitors of histone deacetylase [J].
Chen, WY ;
Bailey, EC ;
McCune, SL ;
Dong, JY ;
Townes, TM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (11) :5798-5803
[6]   ANALYSIS AND DISCRIMINATION OF NECROSIS AND APOPTOSIS (PROGRAMMED CELL-DEATH) BY MULTIPARAMETER FLOW-CYTOMETRY [J].
DIVE, C ;
GREGORY, CD ;
PHIPPS, DJ ;
EVANS, DL ;
MILNER, AE ;
WYLLIE, AH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1992, 1133 (03) :275-285
[7]  
EVANS VJ, 1956, CANCER RES, V16, P77
[8]   Amplification and expression of recombinant genes in serum-independent Chinese hamster ovary cells [J].
Gandor, C ;
Leist, C ;
Fiechter, A ;
Asselbergs, FAM .
FEBS LETTERS, 1995, 377 (03) :290-294
[9]  
HAMILTON WG, 1977, IN VITRO CELL DEV B, V13, P537
[10]  
KAUFMAN RJ, 1990, METHOD ENZYMOL, V185, P537, DOI 10.1016/0076-6879(90)85044-O