The pro‐ or anti‐apoptotic function of NF‐κB is determined by the nature of the apoptotic stimulus
Open Access
- 1 June 2000
- journal article
- research article
- Published by Wiley in European Journal of Biochemistry
- Vol. 267 (12) , 3828-3835
- https://doi.org/10.1046/j.1432-1327.2000.01421.x
Abstract
To test whether the behaviour of transcription factor NF‐κB as a promoter or antagonist of apoptosis depends on the apoptotic stimulus, we determined the influence of NF‐κB on cell killing elicited by a variety of inducers within a given cell type. Inhibition of NF‐κB by genetic and pharmacological approaches rendered HeLa cells more susceptible to TNF‐α‐induced cell killing, but protected them almost completely from H2O2‐ and pervanadate‐induced apoptosis. TNF‐α was unable to protect HeLa from H2O2‐ and pervanadate‐induced apoptosis and further enhanced the cytotoxicity induced by these two adverse agents. Supernatants from HeLa cells stably overexpressing a transdominant negative form of IκB‐α selectively increased the cytotoxicity of TNF‐α for HeLa cells, suggesting that the enhanced susceptibility of these cells can be attributed to one or more secretable factors. Supershift experiments showed that the various apoptotic stimuli induced the same subset of DNA‐binding subunits. Therefore, the nature of the signals elicited by the respective death inducers determines whether NF‐κB induction leads to apoptosis or survival, suggesting that the manipulation of NF‐κB activity may provide a new approach to adjuvant therapy in cancer treatment.Keywords
This publication has 39 references indexed in Scilit:
- Inhibition of tyrosine phosphatases induces apoptosis independent from the CD95 systemCell Death & Differentiation, 1999
- The prosurvival Bcl-2 homolog Bfl-1/A1 is a direct transcriptional target of NF-kappa B that blocks TNFalpha -induced apoptosisGenes & Development, 1999
- Hydrogen peroxide-induced apoptosis is CD95-independent, requires the release of mitochondria-derived reactive oxygen species and the activation of NF-κBOncogene, 1999
- Proteases to die forGenes & Development, 1998
- NF-κB AND REL PROTEINS: Evolutionarily Conserved Mediators of Immune ResponsesAnnual Review of Immunology, 1998
- Sesquiterpene Lactones Specifically Inhibit Activation of NF-κB by Preventing the Degradation of IκB-α and IκB-βJournal of Biological Chemistry, 1998
- Requirement for NF-κB in osteoclast and B-cell developmentGenes & Development, 1997
- Dissection of TNF Receptor 1 Effector Functions: JNK Activation Is Not Linked to Apoptosis While NF-κB Activation Prevents Cell DeathCell, 1996
- THE NF-κB AND IκB PROTEINS: New Discoveries and InsightsAnnual Review of Immunology, 1996
- High levels of c-rel expression are associated with programmed cell death in the developing avian embryo and in bone marrow cells in vitroCell, 1993