| Literature DB >> 15028722 |
Janice M Kelly1, Nigel J Waterhouse, Erika Cretney, Kylie A Browne, Sarah Ellis, Joseph A Trapani, Mark J Smyth.
Abstract
Cell death is mediated by cytotoxic lymphocytes through various granule serine proteases released with perforin. The unique protease activity, restricted expression, and distinct gene locus of granzyme M suggested this enzyme might have a novel biological function or trigger a novel form of cell death. Herein, we demonstrate that in the presence of perforin, the protease activity of granzyme M rapidly and effectively induces target cell death. In contrast to granzyme B, cell death induced by granzyme M does not feature obvious DNA fragmentation, occurs independently of caspases, caspase activation, and perturbation of mitochondria and is not inhibited by overexpression of Bcl-2. These data raise the likelihood that granzyme M represents a third major and specialized perforin-dependent cell death pathway that plays a significant role in death mediated by NK cells.Entities:
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Year: 2004 PMID: 15028722 DOI: 10.1074/jbc.M401670200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157