| Literature DB >> 16751373 |
Fredrik B Thorén1, Ana I Romero, Kristoffer Hellstrand.
Abstract
Cytotoxic T cells and NK cells will acquire features of apoptosis when exposed to oxygen radicals, but the molecular mechanisms underlying this phenomenon are incompletely understood. We have investigated the role of two enzyme systems responsible for execution of cell death, caspases and the poly(ADP-ribose) polymerase (PARP). We report that although human cytotoxic lymphocytes were only marginally protected by caspase inhibitors, PARP inhibitors completely protected lymphocytes from radical-induced apoptosis and restored their cytotoxic function. The radical-induced, PARP-dependent cell death was accompanied by nuclear accumulation of apoptosis-inducing factor and a characteristic pattern of large-fragment DNA degradation. It is concluded that the PARP/apoptosis-inducing factor axis is critically involved in oxygen radical-induced apoptosis in cytotoxic lymphocytes.Entities:
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Year: 2006 PMID: 16751373 DOI: 10.4049/jimmunol.176.12.7301
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422