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Journal of Endotoxin Research
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Pan-caspase inhibitor zVAD enhances cell death in RAW246.7 macrophages

Sung Ouk Kim

Department of Immunology, Scripps Research Institute, La Jolla, California, USA

Jiahuai Han

Department of Immunology, Scripps Research Institute, La Jolla, California, USA, jhan{at}scripps.edu

Even though the pan-caspase inhibitor zVAD has been widely used as an anti-apoptotic agent, inefficient prevention or even enhancement of cell death has been reported in certain cells. To further investigate its effects on cell death, three different cell types were exposed to various apoptotic stimuli in the presence or absence of zVAD. In Jurkat cells, zVAD protected against cell death induced by tumor necrosis factor (TNF), sodium nitroprusside (SNP) and etoposide, whereas in L929 cells cell death was increased. In RAW246.7 macrophages, zVAD showed similar effects as in L929 cells. However, unlike L929 cells, in which the cell death by TNF is known to be necrosis, RAW246.7 cells manifested features of apoptosis such as chromatin condensation and nuclear fragmentation. Induction of cell death by zVAD in lipopolysaccharide (LPS)-activated RAW246.7 cells also showed the same features as those observed in SNP- and etoposide-treated cells. Initiation of an apoptotic process by zVAD not only disputes the sole role of caspases in apoptosis but also suggests an anti-apoptotic function of certain caspase(s). Death of LPS-activated macrophages may be controlled by an anti-apoptotic caspase.

Journal of Endotoxin Research, Vol. 7, No. 4, 292-296 (2001)
DOI: 10.1177/09680519010070041201
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