Activation of caspase-3 in HL-60 cells treated with pyrithione and zinc

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Abstract

The transition metal zinc (Zn) is an endogenous regulator of apoptosis. The ability of Zn to modulate apoptosis is believed to be mediated by the regulation of caspase activity. Previously, we reported that an acute influx of labile Zn induced apoptosis via activation of caspase in human leukemia HL-60 cells treated with a Zn ionophore (Py, pyrithione) and Zn at 1 and 25 μM, respectively. In the present study, we investigated the involvement of caspase-3 in Py (1 μM)/Zn (25 μM)-induced apoptosis in HL-60 cells. Pro-caspase-3 is an inactive form of caspase-3. The processing of pro-caspase-3, a sign of caspase-3 activation, occurred 6 h after treatment with Py/Zn. Proteolysis of poly (ADP-ribose) polymerase (PARP), a substrate of caspase-3, was also observed 6 h after treatment with Py/Zn. We also confirmed the elevation of caspase-3 activity as an index of the cleavage of amino acid sequences recognized by activated caspase-3. An inhibitor of caspase-3 attenuated the appearance of the DNA ladder. Taken together, these results indicate that the activation of caspase-3 is partly responsible for the induction of apoptosis in Py/Zn-treated HL-60 cells. © 2005 Pharmaceutical Society of Japan.

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Kondoh, M., Tasaki, E., Takiguchi, M., Higashimoto, M., Watanabe, Y., & Sato, M. (2005). Activation of caspase-3 in HL-60 cells treated with pyrithione and zinc. Biological and Pharmaceutical Bulletin, 28(4), 757–759. https://doi.org/10.1248/bpb.28.757

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