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Blood, 1 April 2005, Vol. 105, No. 7, pp. 2970-2972.
Prepublished online as a Blood First Edition Paper on November 30, 2004; DOI 10.1182/blood-2004-07-2870.


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PHAGOCYTES
Brief report

z-VAD-fmk augmentation of TNF{alpha}-stimulated neutrophil apoptosis is compound specific and does not involve the generation of reactive oxygen species

Andrew S. Cowburn, Jessica F. White, John Deighton, Sarah R. Walmsley, and Edwin R. Chilvers

From the Department of Medicine, University of Cambridge, Addenbrooke's and Papworth Hospitals, Cambridge, United Kingdom.

In most cell types constitutive and ligand-induced apoptosis is a caspase-dependent process. In neutrophils, however, the broad-spectrum caspase inhibitor z-VAD-fmk enhances tumor necrosis factor-{alpha} (TNF{alpha})-induced cell death, and this has been interpreted as evidence for caspase-dependent and -independent cell death pathways. Our aim was to determine the specificity of the effect of z-VAD-fmk in neutrophils and define the potential mechanism of action. While confirming that z-VAD-fmk (> 100 µM) enhances TNF{alpha}-induced neutrophil apoptosis, lower concentrations (1-30 µM) completely blocked TNF{alpha}-stimulated apoptosis. Boc-D-fmk, a similar broad-spectrum caspase inhibitor, and z-IETD-fmk, a selective caspase-8 inhibitor, caused a concentration-dependent inhibition of only TNF{alpha}-stimulated apoptosis. Moreover, the caspase-9 inhibitor, Ac-LEHD-cmk, had no effect on TNF{alpha}-induced apoptosis, and z-VAD-fmk and Boc-D-fmk inhibited TNF{alpha}-stimulated reactive oxygen species (ROS) generation. These data suggest that TNF{alpha}-induced apoptosis in neutrophils is fully caspase dependent and uses a mitochondrial-independent pathway and that the proapoptotic effects of z-VAD-fmk are compound specific and ROS independent.


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