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Overexpression of bcl‐2 inhibits sodium butyrate‐induced apoptosis in Chinese hamster ovary cells resulting in enhanced humanized antibody production
Author(s) -
Kim No Soo,
Lee Gyun Min
Publication year - 2000
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 - 10.1002/1097-0290(2000)71:3<184::aid-bit1008>3.0.co;2-w
Subject(s) - chinese hamster ovary cell , sodium butyrate , cytotoxic t cell , transfection , biology , microbiology and biotechnology , cell culture , antibody , apoptosis , humanized antibody , immunology , biochemistry , in vitro , monoclonal antibody , genetics
Sodium butyrate (NaBu) can enhance the expression of genes from some of the mammalian promoters including cytomegalovirus (CMV) and simian virus 40 (SV40), but it can also inhibit cell growth and induce cellular apoptosis. Thus, the beneficial effect of using a higher concentration of NaBu on a foreign protein expression is compromised by its cytotoxic effect on cell growth. To overcome this cytotoxic effect of NaBu, a survival protein, human Bcl‐2, was overexpressed in recombinant Chinese hamster ovary (CHO) cells (SH2‐0.32), producing a humanized antibody directed against the S surface antigen of hepatitis B virus. When batch cultures of both control cells transfected with bcl‐2‐ deficient plasmid (SH2‐0.32‐Δbcl‐2) and cells transfected with bcl‐2 expression plasmid (14C6‐bcl‐2) were performed in the absence of NaBu, both cells showed similar profiles of cell viability and antibody production. Compared with the SH2‐0.32‐Δbcl‐2 culture, under the condition of NaBu addition at the exponential growth phase, overexpression of the bcl‐2 gene considerably suppressed the NaBu‐induced apoptosis of 14C6‐bcl‐2 by inhibiting caspase 3 activity and extending culture longevity by >2 days. As a result, the final antibody concentration of 14C6‐bcl‐2 culture was twofold higher than that of SH2‐0.32‐Δbcl‐2 culture in the presence of NaBu and threefold higher than that of SH2‐0.32‐Δbcl‐2 and 14C6‐bcl‐2 cultures in the absence of NaBu. © 2001 John Wiley & Sons, Inc. Biotechnol Bioeng 71: 184–193, 2000/2001.