Gadd45-induced cell cycle G2/M arrest for improved transient gene expression in Chinese hamster ovary cells

被引:5
作者
Kim, Won Hee [1 ]
Kim, Yeon Jung [1 ]
Lee, Gyun Min [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Taejon 305701, South Korea
关键词
CHO cells; transient gene expression (TGE); controlled proliferation; Gadd45; demethylation; RECOMBINANT PROTEIN-PRODUCTION; MAMMALIAN-CELLS; CHO-CELLS; MONOCLONAL-ANTIBODIES; P53-REGULATED PROTEIN; KINASE-ACTIVITY; TRANSFECTION; APOPTOSIS; GADD45; PRODUCTIVITY;
D O I
10.1007/s12257-014-0151-0
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
Gadd45 is a p53-regulated protein and is involved in cell cycle arrest in the G2/M phase. In an effort to improve transient gene expression (TGE) in Chinese hamster ovary (CHO) cells, the effect of Gadd45-induced cell cycle arrest on TGE in CHO cells was investigated using the two different expression vectors encoding Fcfusion protein and recombinant antibody. To regulate the expression of Gadd45 in CHO cells, the CHO-TREx-gadd45 cell line was established using the T-REx system controlled by doxycycline. During the cultures for TGE, Gadd45 overexpression severely inhibited cell growth, but significantly enhanced TGE. Compared with the culture without Gadd45 overexpression, the TGE of Fc fusion protein and humanized antibody were increased by 111 and 93%, respectively. The enhanced TGE, despite the cell growth arrest induced by Gadd45 overexpression, was due to the significantly increased specific productivity, resulting from enhanced transfection efficiency, increased cell size, and active DNA demethylation. Taken together, the data obtained here demonstrate that Gadd45-induced cell cycle arrest in G2/M phase can significantly enhance TGE in CHO cells.
引用
收藏
页码:386 / 393
页数:8
相关论文
共 28 条
[1]   Rational vector design and multi-pathway modulation of HEK 293E cells yield recombinant antibody titers exceeding 1 g/l by transient transfection under serum-free conditions [J].
Backliwal, Gaurav ;
Hildinger, Markus ;
Chenuet, Sebastien ;
Wulhfard, Sarah ;
De Jesus, Maria ;
Wurm, Florian M. .
NUCLEIC ACIDS RESEARCH, 2008, 36 (15)
[2]   Recombinant protein production by large-scale transient gene expression in mammalian cells: state of the art and future perspectives [J].
Baldi, Lucia ;
Hacker, David L. ;
Adam, Myriam ;
Wurm, Florian M. .
BIOTECHNOLOGY LETTERS, 2007, 29 (05) :677-684
[3]  
CARRIER F, 1994, J BIOL CHEM, V269, P32672
[4]   Control of culture environment for improved polyethylenimine-mediated transient production of recombinant monoclonal antibodies by CHO cells [J].
Galbraith, Douglas J. ;
Tait, Andrew S. ;
Racher, Andrew J. ;
Birch, John R. ;
James, David C. .
BIOTECHNOLOGY PROGRESS, 2006, 22 (03) :753-762
[5]   RECOMBINANT PROTEIN PRODUCTION BY TRANSIENT GENE TRANSFER INTO MAMMALIAN CELLS [J].
Geisse, Sabine ;
Fux, Cornelia .
GUIDE TO PROTEIN PURIFICATION, SECOND EDITION, 2009, 463 :223-238
[6]   Methylation of episomal plasmids as a barrier to transient gene expression via a synthetic delivery vector [J].
Hong, K ;
Sherley, J ;
Lauffenburger, DA .
BIOMOLECULAR ENGINEERING, 2001, 18 (04) :185-192
[7]   Effect of doxycycline-regulated ERp57 expression on specific thrombopoietin productivity of recombinant CHO cells [J].
Hwang, SO ;
Chung, JY ;
Lee, GM .
BIOTECHNOLOGY PROGRESS, 2003, 19 (01) :179-184
[8]   Nutrient deprivation induces autophagy as well as apoptosis in Chinese hamster ovary cell culture [J].
Hwang, Sun Ok ;
Lee, Gyun Min .
BIOTECHNOLOGY AND BIOENGINEERING, 2008, 99 (03) :678-685
[9]   GADD45-induced cell cycle G2-M arrest associates with altered subcellular distribution of cyclin B1 and is independent of p38 kinase activity [J].
Jin, SQ ;
Tong, T ;
Fan, WH ;
Fan, FY ;
Antinore, MJ ;
Zhu, XC ;
Mazzacurati, L ;
Li, XX ;
Petrik, KL ;
Rajasekaran, B ;
Wu, M ;
Zhan, QM .
ONCOGENE, 2002, 21 (57) :8696-8704
[10]   Optimization of tetracycline-responsive recombinant protein production and effect on cell growth and ER stress in mammalian cells [J].
Jones, J ;
Nivitchanyong, T ;
Giblin, C ;
Ciccarone, V ;
Judd, D ;
Gorfien, S ;
Krag, SS ;
Betenbaugh, MJ .
BIOTECHNOLOGY AND BIOENGINEERING, 2005, 91 (06) :722-732