Literature DB >> 18623032

Induction of apoptosis in nutrient-deprived cultures of hybridoma and myeloma cells.

S Mercille1, B Massie.   

Abstract

In the present study, cell death was investigated in cultures of NS/0 myelomas and SP2/0-derived D5 hybridomas through morphological examination of cells stained with acridine orange and ethidium bromide. The relative contribution of elevated levels of lactic acid and ammonia, as well as deprivation of glutamine, cystine, and glucose on the induction of necrosis or apoptosis, was investigated. In batch culture of D5 hybridoma cells, induction of apoptotic cell death correlated with the exhaustion of glutamine, while in the case of NS/0 myelomas, it coincided with exhaustion of cystine. To determine whether limiting nutrients were the actual triggering factors for apoptosis in batch culture, exponentially growing cells were resuspended in glutamine or cystine-free media. Within 30 to 40 h, viability decreased to 50% and the nonviable cell population displayed typical apoptotic morphology, with crescents of condensed chromatin around the periphery of the nucleus, or with the entire nucleus present as one or a group of featureless, brightly staining spherical beads. Similarly, D5 hybridomas and NS/0 myelomas cultivated in glucose-free medium died mainly from apoptosis. Cells were also cultivated in fresh medium supplemented with elevated concentrations of ammonia (3.0 mM) and/or lactate (35 mM, 50 mM). This resulted in decreased viabilities and necrotic death in both cell lines. From these results, we conclude that D5 hybridomas and NS/0 myelomas deprived of essential nutrients die by apoptosis, whereas incubation in the presence of elevated levels of metabolic byproducts such as ammonia and lactate will induce necrotic cell death in these cells.

Entities:  

Year:  1994        PMID: 18623032     DOI: 10.1002/bit.260440916

Source DB:  PubMed          Journal:  Biotechnol Bioeng        ISSN: 0006-3592            Impact factor:   4.530


  49 in total

1.  Control of redox potential in hybridoma cultures: effects on MAb production, metabolism, and apoptosis.

Authors:  Angélica Meneses-Acosta; Alfonso Gómez; Octavio T Ramírez
Journal:  J Ind Microbiol Biotechnol       Date:  2012-04-17       Impact factor: 3.346

2.  Hybridomas in a bioreactor cascade: modeling and determination of growth and death kinetics.

Authors:  W A Bakker; T Schäfer; H H Beeftink; J Tramper; C D De Gooijer
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

3.  Amino acid metabolism during batch culture of a murine hybridoma, AFP-27.

Authors:  C P Marquis; J P Barford; C Harbour
Journal:  Cytotechnology       Date:  1996-06       Impact factor: 2.058

4.  Characterization and fed-batch culture of hybridoma overexpressing apoptosis suppressing gene bcl-2.

Authors:  S Terada; Y Itoh; H Ueda; E Suzuki
Journal:  Cytotechnology       Date:  1997-07       Impact factor: 2.058

5.  Cell suicide in starving hybridoma culture: survival-signal effect of some amino acids.

Authors:  F Franěk; K Srámková
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

6.  Apoptosis and its control in cell culture systems.

Authors:  R P Singh; G Finka; A N Emery; M Al-Rubeai
Journal:  Cytotechnology       Date:  1997-01       Impact factor: 2.058

7.  The effect of dissolved oxygen tension and the utility of oxygen uptake rate in insect cell culture.

Authors:  L A Palomares; O T Ramirez
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

8.  The crystal violet nuclei staining technique leads to anomalous results in monitoring mammalian cell cultures.

Authors:  J M Berry; E Huebner; M Butler
Journal:  Cytotechnology       Date:  1996-01       Impact factor: 2.058

9.  Cell suicide in starving hybridoma culture: survival-signal effect of some amino acids.

Authors:  F Franěk; K Srámková
Journal:  Cytotechnology       Date:  1997-01       Impact factor: 2.058

10.  Descriptive parameter evaluation in mammalian cell culture.

Authors:  R L Dutton; J M Scharer; M Moo-Young
Journal:  Cytotechnology       Date:  1998-03       Impact factor: 2.058

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