Expression of the transcription factor GADD153 is an indicator of apoptosis for recombinant chinese hamster ovary (CHO) cells

• Published in: Biotechnology and bioengineering Vol. 75; no. 6; pp. 621 - 629
• Main Authors: Murphy, Tracy C., Woods, Nigel R., Dickson, Alan J.
• Format: Journal Article
• Language: English
• Published: New York John Wiley & Sons, Inc 20.12.2001; Wiley
• Subjects: Animal cells; Animals; Apoptosis; Base Sequence; Biological and medical sciences; Biotechnology; CCAAT-Enhancer-Binding Proteins - genetics; CHO Cells; CHOP; Cricetinae; Culture Media; DNA Primers; Endoplasmic Reticulum - metabolism; Establishment of new cell lines, improvement of cultural methods, mass cultures; Eukaryotic cell cultures; Fundamental and applied biological sciences. Psychology; Methods. Procedures. Technologies; nutrient depletion; recombinant CHO cells; stress; Transcription Factor CHOP; Transcription Factors - genetics; Cell culture; Vertebrata; Cell line; Mammalia; Animal; Rodentia; Recombinant cell; Gene expression; Hamster; CHO cell line; Stress; Apoptosis
• ISSN: 0006-3592; 1097-0290
• DOI: 10.1002/bit.1190

Loss of cell viability, through engagement of apoptotic cell death, represents a limitation to maintenance of high levels of productivity of recombinant animal cells in culture. The ability to monitor the status of recombinant cells, and to define indicators of their “well‐being,” would present a valuable approach to permit a rational intervention at appropriate times during culture. Growth arrest and DNA damage gene 153 (GADD153) is a member of the CCAAT/enhancer‐binding protein (C/EBP) family of transcription factors and has been associated with apoptosis. We have examined the expression of GADD153 in conditions associated with apoptosis of recombinant CHO cells in batch culture. GADD153 expression is very low in CHO cells growing in the exponential phase of batch culture but is activated as cells enter the decline phase. Depletion of nutrients (glucose or glutamine) causes activation of GADD153 expression as does the imposition of endoplasmic reticulum stress. In all cases, there is a good relationship between the extent of apoptosis that occurs in response to each stress and the degree of GADD153 expression. In addition, nutrient refeeding or reversal of stress produces a concomitant decrease in expression of GADD153 and the susceptibility to apoptosis. Thus, GADD153 appears to offer a valid indicator of apoptosis and illustrates the potential for definition of monitors of cellular status related to the likelihood of apoptosis of cell populations. © 2001 John Wiley & Sons, Inc. Biotechnol Bioeng 75: 621–629, 2001.