cMyc increases cell number through uncoupling of cell division from cell size in CHO cells

BMC Biotechnology. 2009;9(1):76 DOI 10.1186/1472-6750-9-76

 

Journal Homepage

Journal Title: BMC Biotechnology

ISSN: 1472-6750 (Online)

Publisher: BMC

LCC Subject Category: Technology: Chemical technology: Biotechnology

Country of publisher: United Kingdom

Language of fulltext: English

Full-text formats available: PDF, HTML

 

AUTHORS

Kuystermans Darrin
Al-Rubeai Mohamed

EDITORIAL INFORMATION

Blind peer review

Editorial Board

Instructions for authors

Time From Submission to Publication: 20 weeks

 

Abstract | Full Text

<p>Abstract</p> <p>Background</p> <p>Over the past decades, the increase in maximal cell numbers for the production of mammalian derived biologics has been in a large part due to the development of optimal feeding strategies. Engineering of the cell line is one of probable approaches for increasing cell numbers in bioreactor.</p> <p>Results</p> <p>We have demonstrated that the over-expression of the <it>c-myc </it>gene in immortalised CHO cells can increase proliferation rate and maximal cell density in batch culture compared to the control. The changes were attributed to a rapid transition into S-phase from a shortened duration of G<sub>1 </sub>phase and to the uncoupling of cell size from cell proliferation. To achieve the >70% increase in maximal cell density without additional supply of nutrients the cells underwent an overall reduction of 14% in size as well as a significant decrease in glucose and amino acid consumption rate. Consequently, the total biomass accumulation did not show a significant change from the control. The amount of hSEAP-hFc activity of the over expressing <it>c-myc </it>cell line was found to be within 0.7% of the control.</p> <p>Conclusion</p> <p>It is shown that the manipulation of cell cycle kinetics and indirectly cell metabolism gives higher cell densities in CHO batch cultures. The unaltered apoptotic rate supported the proposition that the increase in cell number was a result of enhance cell cycle kinetics and cellular metabolism rather than increasing viability. Production of hSEAP-hFc from a constitutive <it>c-myc </it>over-expressing cell line did not increase with the increase in cell number.</p>