Blocking granule-mediated death by primary human NK cells requires both protection of mitochondria and inhibition of caspase activity

Karin A Sedelies, Annette Ciccone, Chris J P Clarke, Jane Oliaro, Vivien R Sutton, Fiona L Scott, J Silke, O Susanto, D R Green, Ricky W Johnstone, Phillip Ian Bird, Joseph A Trapani, N J Waterhouse

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Abstract

Human GraB (hGraB) preferentially induces apoptosis via Bcl-2-regulated mitochondrial damage but can also directly cleave caspases and caspase substrates in cell-free systems. How hGraB kills cells when it is delivered by cytotoxic lymphocytes (CL) and the contribution of hGraB to CL-induced death is still not clear. We show that primary human natural killer (hNK) cells, which specifically used hGraB to induce target cell death, were able to induce apoptosis of cells whose mitochondria were protected by Bcl-2. Purified hGraB also induced apoptosis of Bcl-2-overexpressing targets but only when delivered at 5- to 10-fold the concentration required to kill cells expressing endogenous Bcl-2. Caspases were critical in this process as inhibition of caspase activity permitted clonogenic survival of Bcl-2-overexpressing cells treated with hGraB or hNK cells but did not protect cells that only expressed endogenous Bcl-2. Our data therefore show that hGraB triggers caspase activation via mitochondria-dependent and mitochondria-independent mechanisms that are activated in a hierarchical manner, and that the combined effects of Bcl-2 and direct caspase inhibition can block cell death induced by hGraB and primary hNK cells.
Original languageEnglish
Pages (from-to)708 - 717
Number of pages10
JournalCell Death and Differentiation
Volume15
Issue number4
Publication statusPublished - 2008

Cite this

Sedelies, K. A., Ciccone, A., Clarke, C. J. P., Oliaro, J., Sutton, V. R., Scott, F. L., Silke, J., Susanto, O., Green, D. R., Johnstone, R. W., Bird, P. I., Trapani, J. A., & Waterhouse, N. J. (2008). Blocking granule-mediated death by primary human NK cells requires both protection of mitochondria and inhibition of caspase activity. Cell Death and Differentiation, 15(4), 708 - 717.