Activation of caspase-like proteases and induction of apoptosis by isopentenyladenosine in tobacco BY-2 cells
Language English Country Germany Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
- MeSH
- Enzyme Activation drug effects MeSH
- Apoptosis drug effects MeSH
- Amino Acid Chloromethyl Ketones pharmacology MeSH
- Cytokinins pharmacology MeSH
- Endopeptidases metabolism MeSH
- Caspase Inhibitors MeSH
- Isopentenyladenosine pharmacology MeSH
- Caspase 1 metabolism MeSH
- Caspase 3 MeSH
- Caspases metabolism MeSH
- Cells, Cultured MeSH
- Oligopeptides pharmacology MeSH
- Plant Growth Regulators pharmacology MeSH
- Nicotiana cytology drug effects metabolism MeSH
- Dose-Response Relationship, Drug MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- benzoylcarbonyl-aspartyl-glutamyl-valyl-aspartyl-fluoromethyl ketone MeSH Browser
- benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone MeSH Browser
- Amino Acid Chloromethyl Ketones MeSH
- Cytokinins MeSH
- Endopeptidases MeSH
- Caspase Inhibitors MeSH
- Isopentenyladenosine MeSH
- Caspase 1 MeSH
- Caspase 3 MeSH
- Caspases MeSH
- Oligopeptides MeSH
- Plant Growth Regulators MeSH
The effects of isopentenyladenosine (iPA) on tobacco (Nicotiana tabacum L.) BY-2 cells were examined. The number of BY-2 cells decreased in a time- and concentration-dependent manner after being exposed to micromolar concentrations of iPA. This decrease was mainly due to a loss of cell viability, since no substantial changes in cell cycle progression were revealed by flow-cytometric analysis. Dying cells exhibited the typical morphological and biochemical hallmarks of apoptosis, including cell shrinkage, chromatin condensation, and degradation of nuclear DNA to nucleosomal size fragments. Caspase-1-like and caspase-3-like proteases also became activated, the former being dominant. Inhibitor-sensitivity studies revealed that although synthetic caspase inhibitors failed to prevent cell death they markedly reduced cell death in tobacco BY-2 cells, Nu-benzyloxycarbonyl-Val-Ala-Asp-fluoromethylketone, a specific inhibitor for caspase-1, being the most effective. Our results indicate that caspase-like proteases, and particularly caspase-1-like protease, might be critically implicated in iPA-induced apoptosis of BY-2 cells. Finally, the outcome of inhibiting adenosine kinase by 4-amino-3-iodo-1(beta- D-ribofuranosyl)pyrazolo[3,4-d]-pyrimidine revealed that intracellular phosphorylation of iPA is required for its cytotoxicity to develop.
References provided by Crossref.org
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