Forskolin Increases cAMP Levels and Enhances Recombinant Antibody Production in CHO Cell Cultures

被引:9
作者
Yoon, Chansik [1 ]
Kim, Dongil [1 ]
Lim, Ju Hyeon [2 ]
Lee, Gyun Min [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Biol Sci, Daejeon 34141, South Korea
[2] New Drug Dev Ctr, Cheongju 28160, South Korea
关键词
cAMP; cell cycle; CHO cell; forskolin; specific productivity; BCL-2; EXPRESSION; EFFECTOR FUNCTIONS; RESPONSE ELEMENT; SODIUM-BUTYRATE; CYCLE ARREST; STEM-CELLS; AUTOPHAGY; CREB; PHOSPHORYLATION; GROWTH;
D O I
10.1002/biot.202000264
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cyclic adenosine monophosphate (cAMP) is a ubiquitous second messenger essential to many biological processes. Forskolin, a labdane diterpene, is widely used to increase cAMP levels in various cell types. When 5 mu mof forskolin is added to recombinant Chinese hamster ovary (rCHO) cell cultures producing monoclonal antibody (mAb) (GSR cell line), it decreases specific growth rate (mu), but increases culture longevity and specific mAb productivity (q(mAb)). The beneficial effect of forskolin on culture longevity andq(mAb)outweighs its detrimental effect on mu, resulting in 1.5-fold increase in the maximum mAb concentration (MMC) without an adverse effect on mAb quality attributes such as aggregation, charge variation, and galactosylation. Forskolin induces cell cycle arrest at the G0/G1 phase via the LKB1/AMPK pathway and inhibits apoptosis via the CREB/Bcl-2 pathway. The beneficial effect of forskolin on mAb production is also demonstrated with another rCHO cell line (ABTAA). Addition of 5 mu mforskolin to ABTAA cell cultures also results in 1.5-fold increase in the MMC. Taken together, the results obtained demonstrate that forskolin is an efficient chemical reagent to increase mAb production in rCHO cell cultures.
引用
收藏
页数:9
相关论文
共 67 条
[1]   Effects of nutrient levels and average culture pH on the glycosylation pattern of camelid-humanized monoclonal antibody [J].
Aghamohseni, Hengameh ;
Ohadi, Kaveh ;
Spearman, Maureen ;
Krahn, Natalie ;
Moo-Young, Murray ;
Scharer, Jeno M. ;
Butler, Mike ;
Budman, Hector M. .
JOURNAL OF BIOTECHNOLOGY, 2014, 186 :98-109
[2]   Forskolin and derivatives as tools for studying the role of cAMP [J].
Alasbahi, R. H. ;
Melzig, M. F. .
PHARMAZIE, 2012, 67 (01) :5-13
[3]   CREB and the CRTC co-activators: sensors for hormonal and metabolic signals [J].
Altarejos, Judith Y. ;
Montminy, Marc .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2011, 12 (03) :141-151
[4]   ERK implication in cell cycle regulation [J].
Chambard, Jean-Claude ;
Lefloch, Renaud ;
Pouyssegur, Jacques ;
Lenormand, Philippe .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2007, 1773 (08) :1299-1310
[5]   N-acetylcysteine increases the biosynthesis of recombinant EPO in apoptotic Chinese hamster ovary cells [J].
Chang, KH ;
Kim, KS ;
Kim, JH .
FREE RADICAL RESEARCH, 1999, 30 (02) :85-91
[6]   Epac and PKA: a tale of two intracellular cAMP receptors [J].
Cheng, Xiaodong ;
Ji, Zhenyu ;
Tsalkova, Tamara ;
Mei, Fang .
ACTA BIOCHIMICA ET BIOPHYSICA SINICA, 2008, 40 (07) :651-662
[7]   Regulation of the autophagy protein LC3 by phosphorylation [J].
Cherra, Salvatore J., III ;
Kulich, Scott M. ;
Uechi, Guy ;
Balasubramani, Manimalha ;
Mountzouris, John ;
Day, Billy W. ;
Chu, Charleen T. .
JOURNAL OF CELL BIOLOGY, 2010, 190 (04) :533-539
[8]   Effects of forskolin on Kupffer cell production of interleukin-10 and tumor necrosis factor alpha differ from those of endogenous adenylyl cyclase activators: Possible role for adenylyl cyclase 9 [J].
Dahle, MK ;
Myhre, AE ;
Aasen, AO ;
Wang, JE .
INFECTION AND IMMUNITY, 2005, 73 (11) :7290-7296
[9]   Use of a Small Molecule Cell Cycle Inhibitor to Control Cell Growth and Improve Specific Productivity and Product Quality of Recombinant Proteins in CHO Cell Cultures [J].
Du, Zhimei ;
Treiber, David ;
McCarter, John D. ;
Fomina-Yadlin, Dina ;
Saleem, Ramsey A. ;
McCoy, Rebecca E. ;
Zhang, Yuling ;
Tharmalingam, Tharmala ;
Leith, Matthew ;
Follstad, Brian D. ;
Dell, Brad ;
Grisim, Brent ;
Zupke, Craig ;
Heath, Carole ;
Morris, Arvia E. ;
Reddy, Pranhitha .
BIOTECHNOLOGY AND BIOENGINEERING, 2015, 112 (01) :141-155
[10]   Bile acid stimulates hepatocyte polarization through a cAMP-Epac-MEK-LKB1-AMPK pathway [J].
Fu, Dong ;
Wakabayashi, Yoshiyuki ;
Lippincott-Schwartz, Jennifer ;
Arias, Irwin M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (04) :1403-1408