Characterization of apoptosis in PER.C6® batch and perfusion cultures

• Published in: Biotechnology and bioengineering 2015-03, Vol.112 (3), p.569-578
• Main Authors: Mercier, Sarah M., Diepenbroek, Bas, Martens, Dirk, Wijffels, Rene H., Streefland, Mathieu
• Format: Article
• Language: English
• Subjects: adenovirus; Apoptosis; Apoptosis - physiology; Batch Cell Culture Techniques; Bioreactors; Biotechnology; Carbon sources; Caspases - metabolism; Cell culture; Cell Line, Transformed; Cell Proliferation - physiology; Cell Survival - physiology; Cellular biology; death; Deoxyribonucleic acid; DNA; Flow cytometry; gene; hamster ovary cells; high-level expression; Humans; line per.c6; manufacture; Mortality; PER.C6; perfusion; vaccine
• ISSN: 0006-3592; 1097-0290
• DOI: 10.1002/bit.25459

ABSTRACT Preventing or delaying cell death is a challenge in mammalian cell cultures for the development and optimization of production processes for biopharmaceuticals. Cell cultures need to be maintained highly viable for extended times in order to reach maximum production yields. Moreover, programmed cell death through apoptosis is often believed to occur without being detected by classical viability measurements. In this study, we characterized cell death in PER.C6® batch and perfusion cultures using three flow cytometry techniques measuring different steps of the apoptosis cascade: DNA fragmentation, caspases activation and phosphatidylserine externalization. We showed that apoptosis is the main pathway of PER.C6® cell death in batch cultures after depletion of main carbon sources. In high cell density perfusion cultures fed at a constant specific perfusion rate, both high viability and very limited apoptosis were observed. When extending this perfusion process far beyond standard operations, cultures were exposed to suboptimal process conditions, which resulted in an increase of apoptotic cell death. Moreover, we showed that the reference viability measurement using trypan blue exclusion properly assesses the level of cell death in PER.C6® cultures. This study is a first step in understanding the mechanisms of PER.C6® cell death, which will be helpful to support applications of the cell line. Biotechnol. Bioeng. 2015;112: 569–578. © 2014 Wiley Periodicals, Inc. Cell death was characterized in PER.C6® batch and perfusion cultures using three flow cytometry techniques measuring different steps of the apoptosis cascade: DNA fragmentation, caspases activation and phosphatidylserine externalization. The authors showed that apoptosis is the main pathway of PER.C6® cell death in batch cultures whereas in high cell density perfusion cultures fed at a constant specific perfusion rate, both high viability and very limited apoptosis were observed.