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Serum protects protein‐free competent Chinese hamster ovary cells against apoptosis induced by nutrient deprivation in batch culture
Author(s) -
Zanghi James A.,
Fussenegger Martin,
Bailey James E.
Publication year - 1999
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/(sici)1097-0290(19990705)64:1<108::aid-bit12>3.0.co;2-b
Subject(s) - chinese hamster ovary cell , apoptosis , fetal bovine serum , cell culture , programmed cell death , biology , cell growth , microbiology and biotechnology , cell , biochemistry , genetics
The development of serum‐ and protein‐free Chinese hamster ovary (CHO) cell cultures is a high priority for the production of biopharmaceuticals. Protein‐free competent CHO cells lines have been previously constructed by two different methods—metabolic engineering with cell‐cycle regulatory proteins and long‐term selective adaptation. Apoptosis was present in both cell lines during protein‐free, static‐batch culture as a result of nutrient deprivation, and glucose deprivation alone was a potent inducer of apoptosis compared to the depletion of other nutrients such as amino acids. By adding back serum to the cultures during batch growth or nutrient deprivation, it was shown that unidentified survival factors in serum can greatly reduce apoptosis in protein‐competent cell lines in all phases of the culture. Both observations contrast to previous reports for hybridoma cells, in which amino acids were the key determinants of apoptosis and serum had no additional antiapoptotic effect. Serum's protective effect against CHO cell death in batch culture was multifaceted and complex: (1) 10% FBS increased cell viability to >99% during exponential growth from roughly 75–90%, (2) 5–10% fetal bovine serum (FBS) reduced specific glucose consumption rates in both cell lines by 40%, thereby delaying the onset of apoptosis caused by glucose deprivation, and (3) 5% FBS reduced the specific cell death rate by 65% during a 3‐d lactate‐consumption phase characterized by substantial abortive proliferation, in which the cells both proliferated and died at a constant rate. The benefit of serum on cell production over the various phases of batch growth was combined into a single parameter by integrating the viable cell concentration vs. time profile (termed here as cumulative volumetric viable cell‐time, VCT vol ). Despite the ability of both cell lines to grow indefinitely without any exogenous growth factors, the addition of serum resulted in a 2.3‐fold increase in the VCT vol . Thus, it is clear that there is much room for improvement of protein‐free CHO cell lines despite their adequate growth competence, and new strategies different from those successfully used for hybridomas may be necessary to combat CHO cell apoptosis. © 1999 John Wiley & Sons, Inc. Biotechnol Bioeng 64: 108–119, 1999.