Caspases-3 and -7 are activated in goniothalamin-induced apoptosis in human Jurkat T-cells

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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. Copyright (C) 1999 Federation of European Biochemical Societies.

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Inayat-Hussain, S. H., Osman, A. B., Din, L. B., Ali, A. M., Snowden, R. T., MacFarlane, M., & Cain, K. (1999). Caspases-3 and -7 are activated in goniothalamin-induced apoptosis in human Jurkat T-cells. FEBS Letters, 456(3), 379–383. https://doi.org/10.1016/S0014-5793(99)00984-9

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