2000
DOI: 10.1006/bbrc.2000.2166
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Activation of Caspase-3 in Molt4 Cells by Apoptosis-Inducing Nucleosides from CD57+HLA-DRbright Natural Suppressor Cell Line

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Cited by 5 publications
(2 citation statements)
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“…This result confirmed the involvement of caspase-3, which is activated by sequential proteolytic events that cleave the 32-kDa precursor at aspartic acid residues to generate an active heterodimer of 20-and 12-kDa subunits, 45) corresponding to our recent findings. 46) The active caspase-3, in turn, cleaves the inhibitor of caspase-activated DNase (ICAD) and then activates the caspase-activated DNase (CAD), which migrates to the nucleus and degrades DNA. 47) We consider that AINs are good candidates for anticancer agents, and we are planning further studies on AINs-induced apoptosis in various malignant target cells.…”
Section: Discussionmentioning
confidence: 99%
“…This result confirmed the involvement of caspase-3, which is activated by sequential proteolytic events that cleave the 32-kDa precursor at aspartic acid residues to generate an active heterodimer of 20-and 12-kDa subunits, 45) corresponding to our recent findings. 46) The active caspase-3, in turn, cleaves the inhibitor of caspase-activated DNase (ICAD) and then activates the caspase-activated DNase (CAD), which migrates to the nucleus and degrades DNA. 47) We consider that AINs are good candidates for anticancer agents, and we are planning further studies on AINs-induced apoptosis in various malignant target cells.…”
Section: Discussionmentioning
confidence: 99%
“…The oocytes were previously stimulated by anti-Fas mAb (1 µg/ml) at 37 °C for 6 h. A single cell assay that relies on the liberation of AMC (7-amino-4-methylcoumarin) cleaved from the caspase-3 substrate peptide DEVD (Asp-Glu-Val-Asp) (Li et al, 2000) was applied for morphological detection of caspase-3 activity in oocytes. The caspase-3 substrate AMC-conjugated DEVD prepared according to the manufacturer's protocol (PharMingen) was added to a suspension of oocytes and incubated for 2 h. The oocytes were fixed in 2% paraformaldehyde-PBS for 30 min, followed by a permeabilisation step of incubation in 0.2% Triton X-100-PBS for 10 min.…”
Section: Single Cell Assay Of Caspase-3 Activitymentioning
confidence: 99%