Mitochondrial Membrane Potential Selects Hybridomas Yielding High Viability in Fed‐Batch Cultures
- 1 January 2002
- journal article
- Published by Wiley in Biotechnology Progress
- Vol. 18 (1) , 1-5
- https://doi.org/10.1021/bp010132b
Abstract
Prior research (Follstad, B. D.; Wang, D. I. C.; Stephanopoulos, G. Mitochondrial membrane potential differentiates cells resistant to apoptosis in hybridoma cultures. Eur. J. Biochem. 2000, 267, 6534-6540.) identified mitochondrial membrane potential (MMP) as a marker of hybridoma subpopulations resistant to apoptosis caused by a variety of apoptosis inducers. In this study, we investigated the viability of hybridoma cell cultures inoculated with cells of varying MMP in regular fed-batch operation. A hybridoma cell population was separated using FACS into subpopulations based on their mean mitochondrial membrane potential (MMP) as measured using the common mitochondrial stain, Rhodamine 123 (Rh123). These subpopulations showed dramatic differences in their apoptotic death kinetics. Fed-batches inoculated with a high MMP subpopulation reached higher viable cell concentrations and viabilities that were maintained for prolonged periods of time relative to fed-batches inoculated with low MMP subpopulations. These results underline the heterogeneous nature of hybridoma cell cultures and suggest that mitochondrial physiology is a critical parameter determining culture performance.Keywords
This publication has 21 references indexed in Scilit:
- Apoptosis-resistant Mitochondria in T Cells Selected for Resistance to Fas SignalingJournal of Biological Chemistry, 2001
- Mitochondria and ApoptosisScience, 1998
- High viable cell concentration fed‐batch cultures of hybridoma cells through on‐line nutrient feedingBiotechnology & Bioengineering, 1995
- Induction of apoptosis in nutrient‐deprived cultures of hybridoma and myeloma cellsBiotechnology & Bioengineering, 1994
- Catabolic control of hybridoma cells by glucose and glutamine limited fed batch culturesBiotechnology & Bioengineering, 1994
- Fed‐batch cultivation of animal cells using different medium design concepts and feeding strategiesBiotechnology & Bioengineering, 1994
- Stoichiometric analysis of animal cell growth and its application in medium designBiotechnology & Bioengineering, 1994
- Genetically engineering mammalian cell lines for increased viability and productivityBiotechnology Advances, 1994
- Monoclonal Antibody Process Development Using Medium ConcentratesBiotechnology Progress, 1994
- Reduction of waste product excretion via nutrient control: Possible strategies for maximizing product and cell yields on serum in cultures of mammalian cellsBiotechnology & Bioengineering, 1986