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• W2107385283 abstract "A number of pro-apoptotic stimuli induce the activation of caspase-9, an initiator protease that activates executioner caspases, such as caspase-3, leading to the development of programmed cell death. Here we demonstrate that cell (platelets and pancreatic acinar cells) stimulation with agonists induces a bimodal activation of caspase-3. The early caspase-3 activation occurs within 1 min of stimulation and is independent on caspase-9 or mitochondrial cytochrome c release suggesting that is a non-apoptotic event. The ability of agonists to induce early activation of caspase-3 is similar to that observed for other physiological processes. Activation of caspase-3 by physiological concentrations of cellular agonists, including thrombin or CCK-8, is independent of rises in cytosolic calcium concentration but requires PKC activation, and is necessary for agonist-induced activation of the tyrosine kinases Btk and pp60src and for several cellular functions, including store-operated calcium entry, platelet aggregation, or pancreatic secretion. Thus, early activation of caspase-3 seems to be a non-apoptotic event required for cellular function." @default.
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• W2107385283 date "2006-06-21" @default.
• W2107385283 modified "2023-10-09" @default.
• W2107385283 title "Early caspase-3 activation independent of apoptosis is required for cellular function" @default.
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• W2107385283 doi "https://doi.org/10.1002/jcp.20715" @default.
• W2107385283 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16791842" @default.
• W2107385283 hasPublicationYear "2006" @default.
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