Hybridoma cell cultures continuously undergo apoptosis and reveal a novel 100 bp DNA fragment.

This report represents an investigation into the nature of apoptosis in hybridoma cultures and its significance to their utilization in biotechnology. To this end DNA fragmentation and capillary electrophoresis of genomic DNA was studied during the culture of two hybridoma cell lines. This indicated that the phenomenon of apoptosis was always present even under normal culture conditions. Two DNA fragments not associated with the typical DNA fragmentation ladder were identified in the two hybridoma cultures: a previously unreported DNA fragment of about 100 bp and a large fragment which may correspond to one reported in the literature (Walker et al., 1993). The small fragment was identified as soon as the early exponential growth phase of culture, while the large fragment appeared only in the latter part of the growth curve when there was marked DNA fragmentation. In addition we present evidence that aurintricarboxylic acid, which inhibits apoptosis in neural cells, permits this process in hybridoma cells at levels below 100 microM. This unusual predisposition of hybridoma cultures to undergo apoptosis and their response to inhibitor of apoptosis may have important implications for approaches to the culture of hybridomas and their utilization for monoclonal production.

[1]  F Franĕk,et al.  Nucleosomes occurring in protein‐free hybridoma cell culture Evidence for programmed cell death , 1991, FEBS letters.

[2]  T. Murphy,et al.  Rapid Communication: Oxidative Stress Induces Apoptosis in Embryonic Cortical Neurons , 1994, Journal of neurochemistry.

[3]  R. Todd,et al.  Overall pathway of mononucleosome production. , 1979, The Journal of biological chemistry.

[4]  R. Hebbel,et al.  Internucleosomal cleavage of DNA is insufficient evidence to conclude that cell death is apoptotic. , 1994, Blood.

[5]  J. Dubinsky,et al.  Aurintricarboxylic Acid Protects Hippocampal Neurons from Glutamate Excitotoxicity In Vitro , 1993, Journal of neurochemistry.

[6]  X. M. Sun,et al.  Quantification of apoptosis and necrosis by flow cytometry. , 1993, Acta oncologica.

[7]  L. Tessitore,et al.  The role of apoptosis in growing and stationary rat ascites hepatoma, Yoshida AH‐130 , 1993, The Journal of pathology.

[8]  J. Stoltz,et al.  Monoclonal antibodies against human plasma protein C and their uses for immunoaffinity chromatography. , 1991, Thrombosis research.

[9]  S. Umansky,et al.  The use of flow cytometry for the investigation of cell death. , 1993, Cytometry.

[10]  T. Vomastek,et al.  Kinetics of development of spontaneous apoptosis in B cell hybridoma cultures. , 1993, Immunology letters.

[11]  J. Hickman,et al.  Apoptotic death in epithelial cells: cleavage of DNA to 300 and/or 50 kb fragments prior to or in the absence of internucleosomal fragmentation. , 1993, The EMBO journal.

[12]  A. Wyllie Glucocorticoid-induced thymocyte apoptosis is associated with endogenous endonuclease activation , 1980, Nature.

[13]  P. Walker,et al.  Detection of the initial stages of DNA fragmentation in apoptosis. , 1993, BioTechniques.

[14]  A. Acheson,et al.  Cell and tissue culture laboratory procedures , 1994 .

[15]  A. Eastman Apoptosis: a product of programmed and unprogrammed cell death. , 1993, Toxicology and applied pharmacology.

[16]  M. Collins,et al.  The control of apoptosis in mammalian cells. , 1993, Trends in biochemical sciences.

[17]  L. Rubin,et al.  The cell cycle and cell death , 1993, Current Biology.

[18]  L. Ghibelli,et al.  The expression of "tissue" transglutaminase in two human cancer cell lines is related with the programmed cell death (apoptosis). , 1991, European journal of cell biology.

[19]  K. Khanna,et al.  Butyrate induced apoptosis in lymphoid cells preceded by transient over-expression of HSP70 mRNA. , 1994, Biochemical and biophysical research communications.

[20]  W. Bursch,et al.  The biochemistry of cell death by apoptosis. , 1990, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[21]  M. E. Lewis,et al.  Aurintricarboxylic Acid Protects Hippocampal Neurons from NMDA‐and Ischemia‐Induced Toxicity In Vivo , 1993, Journal of neurochemistry.

[22]  Z. Darżynkiewicz,et al.  Features of apoptotic cells measured by flow cytometry. , 1992, Cytometry.

[23]  L. Gerschenson,et al.  Apoptosis: a different type of cell death , 1992, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[24]  E. Wolvetang,et al.  Mitochondrial respiratory chain inhibitors induce apoptosis , 1994, FEBS letters.

[25]  I Nicoletti,et al.  A rapid and simple method for measuring thymocyte apoptosis by propidium iodide staining and flow cytometry. , 1991, Journal of immunological methods.

[26]  D. Schoepp,et al.  Aurintricarboxylic Acid Prevents NMDA‐Mediated Excitotoxicity: Evidence for Its Action as an NMDA Receptor Antagonist , 1993, Journal of neurochemistry.

[27]  D. Green,et al.  Role of DNA fragmentation in T cell activation-induced apoptosis in vitro and in vivo. , 1994, Journal of immunology.