Activation of caspase-like proteases and induction of apoptosis by isopentenyladenosine in tobacco BY-2 cells
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- aktivace enzymů účinky léků MeSH
- apoptóza účinky léků MeSH
- chloromethylketony aminokyselin farmakologie MeSH
- cytokininy farmakologie MeSH
- endopeptidasy metabolismus MeSH
- inhibitory kaspas MeSH
- isopentenyladenosin farmakologie MeSH
- kaspasa 1 metabolismus MeSH
- kaspasa 3 MeSH
- kaspasy metabolismus MeSH
- kultivované buňky MeSH
- oligopeptidy farmakologie MeSH
- regulátory růstu rostlin farmakologie MeSH
- tabák cytologie účinky léků metabolismus MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- benzoylcarbonyl-aspartyl-glutamyl-valyl-aspartyl-fluoromethyl ketone MeSH Prohlížeč
- benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone MeSH Prohlížeč
- chloromethylketony aminokyselin MeSH
- cytokininy MeSH
- endopeptidasy MeSH
- inhibitory kaspas MeSH
- isopentenyladenosin MeSH
- kaspasa 1 MeSH
- kaspasa 3 MeSH
- kaspasy MeSH
- oligopeptidy MeSH
- regulátory růstu rostlin 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.
Citace poskytuje Crossref.org
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