Abstract
Goniothalamin, a plant styrylpyrone derivative isolated from Goniothalamus andersonii, induced apoptosis in Jurkat T-cells as assessed by the externalisation of phosphatidylserine. Immunoblotting showed processing of caspases-3 and -7 with the appearance of their catalytically active large subunits of 17 and 19 kDa, respectively. Activation of these caspases was further evidenced by detection of poly(ADP-ribose) polymerase cleavage (PARP). Pre-treatment with the caspase inhibitor benzyloxycarbonyl-Val-Ala-Asp fluoromethyl ketone (Z-VAD.FMK) blocked apoptosis and the resultant cleavage of these caspases and PARP. Our results demonstrate that activation of at least two effector caspases is a key feature of goniothalamin-induced apoptosis in Jurkat T-cells.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Chloromethyl Ketones / pharmacology
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Annexin A5 / analysis
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Annexin A5 / metabolism
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Apoptosis / drug effects*
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Caspase 3
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Caspase 7
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Caspase Inhibitors
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Caspases / metabolism*
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Cysteine Proteinase Inhibitors / pharmacology
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Enzyme Activation / drug effects
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Humans
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Jurkat Cells / drug effects*
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Jurkat Cells / enzymology
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Jurkat Cells / pathology
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Poly(ADP-ribose) Polymerases / metabolism
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Pyrones / metabolism
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Pyrones / pharmacology*
Substances
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Amino Acid Chloromethyl Ketones
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Annexin A5
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Caspase Inhibitors
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Cysteine Proteinase Inhibitors
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Pyrones
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benzyloxycarbonylvalyl-alanyl-aspartyl fluoromethyl ketone
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goniothalamin
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Poly(ADP-ribose) Polymerases
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CASP3 protein, human
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CASP7 protein, human
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Caspase 3
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Caspase 7
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Caspases