Quantifying the impact of cell culture media on CHO cell growth and protein production

被引:24
作者
Combe, Michelle [1 ]
Sokolenko, Stanislav [1 ]
机构
[1] Dalhousie Univ, Dept Proc Engn & Appl Sci, 1360 Barrington St,POB 15000, Halifax, NS B3H 4R2, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Cell culture; CHO; Media; Additives; Titer; Cell density; Modelling; HAMSTER OVARY CELLS; SERUM-FREE MEDIUM; RECOMBINANT INTERFERON-GAMMA; FC-FUSION PROTEIN; MONOCLONAL-ANTIBODY PRODUCTION; SUSPENSION-CULTURE; T-PA; PLASMINOGEN-ACTIVATOR; HUMAN THROMBOPOIETIN; ENHANCED PRODUCTION;
D O I
10.1016/j.biotechadv.2021.107761
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
In recombinant protein production, cell culture media development and optimization is typically seen as a useful strategy to increase titer and cell density, reduce by-products, as well as improve product quality (with cell density and titer often serving as the primary reported outcome of media studies). However, despite the large number of media optimization studies, there have been few attempts to comprehensively assess the overall effectiveness of media additives. The aim of this review is therefore both to document published media optimization studies over the last twenty years (in the context of Chinese hamster ovary cell recombinant production) and quantitatively estimate the impact of this media optimization on cell culture performance. In considering 78 studies, we have identified 238 unique media components that have been supplemented over the last 20 years. Among these additives, trace elements stood out as having a positive impact on cell density while nucleotides show potential for increasing titer, with commercial supplements benefiting both. However, we also identified that the impact of specific additives is far more variable than often perceived. With relatively few media studies considering multiple cell lines or multiple basal media, teasing out consistent and general trends becomes a considerable challenge. By extracting cell density and titer values from all of the reviewed studies, we were able to build a mixed-effect model capable of estimating the relative impact of additives, cell line, product type, basal medium, cultivation method (flask or reactor), and feeding strategy (batch or fed-batch). Overall, additives only accounted for 3% of the variation in cell density and 1% of the variation in titer. Similarly, the impact of basal media was also relatively modest, at 10% for cell density and 0% for titer. Cell line, product type, and feeding strategy were all found to have more impact. These results emphasize the need for media studies to consider more factors to ensure that reported observations can be generalized and further developed.
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页数:15
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共 110 条
[1]   Improvement of CHO cell culture medium formulation:: Simultaneous substitution of glucose and glutamine [J].
Altamirano, C ;
Paredes, C ;
Cairó, JJ ;
Gòdia, F .
BIOTECHNOLOGY PROGRESS, 2000, 16 (01) :69-75
[2]   Specific nutrient supplementation of defined serum-free medium for the improvement of CHO cells growth and t-PA production [J].
Altamirano, Claudia ;
Illanes, Andres ;
Canessa, Rossana ;
Becerra, Silvana .
ELECTRONIC JOURNAL OF BIOTECHNOLOGY, 2006, 9 (01) :61-67
[3]   Considerations on the lactate consumption by CHO cells in the presence of galactose [J].
Altamirano, Claudia ;
Illanes, Andres ;
Becerra, Silvana ;
Cairo, Jordi Joan ;
Godia, Francesc .
JOURNAL OF BIOTECHNOLOGY, 2006, 125 (04) :547-556
[4]  
Altamirano C, 2013, ELECTRON J BIOTECHN, V16
[5]   Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG fc [J].
Anthony, Robert M. ;
Nimmerjahn, Falk ;
Ashline, David J. ;
Reinhold, Vernon N. ;
Paulson, James C. ;
Ravetch, Jeffrey V. .
SCIENCE, 2008, 320 (5874) :373-376
[6]   Partial Replacement of Chemically Defined CHO Media with Plant-Derived Protein Hydrolysates [J].
Babcock, James E. ;
Antosh, Amy .
PROCEEDINGS OF THE 21ST ANNUAL MEETING OF THE EUROPEAN SOCIETY FOR ANIMAL CELL TECHNOLOGY (ESACT), 2009, 2012, 5 :295-298
[7]   Plant protein hydrolysates support CHO-320 cells proliferation and recombinant IFN-γ production in suspension and inside microcarriers in protein-free media [J].
Ballez, JS ;
Mols, J ;
Burteau, C ;
Agathos, SN ;
Schneider, YJ .
CYTOTECHNOLOGY, 2004, 44 (03) :103-114
[8]  
Baré G, 2001, ESACT PROCEED, V1, P217
[9]   Fitting Linear Mixed-Effects Models Using lme4 [J].
Bates, Douglas ;
Maechler, Martin ;
Bolker, Benjamin M. ;
Walker, Steven C. .
JOURNAL OF STATISTICAL SOFTWARE, 2015, 67 (01) :1-48
[10]   An omics approach to rational feed Enhancing growth in CHO cultures with NMR metabolomics and 2D-DIGE proteomics [J].
Blondeel, Eric J. M. ;
Ho, Raymond ;
Schulze, Steffen ;
Sokolenko, Stanislav ;
Guillemette, Simon R. ;
Slivac, Igor ;
Durocher, Yves ;
Guillemette, J. Guy ;
McConkey, Brendan J. ;
Chang, David ;
Aucoin, Marc G. .
JOURNAL OF BIOTECHNOLOGY, 2016, 234 :127-138