Journal
FREE RADICAL BIOLOGY AND MEDICINE
Volume 48, Issue 6, Pages 791-797Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2009.12.020
Keywords
Apoptosis-inducing factor; Calcium; Reactive oxygen species; Carbonylation; Calpain; Mitochondria; Apoptosis; Free radicals
Funding
- Swedish Research Council
- Swedish and the Stockholm Cancer Societies
- Swedish Childhood Cancer Foundation
- EC FP-6
- FP7 (Apo-Sys) programs
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Although processing of mitochondrial apoptosis-inducing factor (AIF) is essential for its function during apoptosis in most cell types, the detailed mechanisms of AIF cleavage remain elusive. Recent findings indicate that the proteolytic process is Ca2+-dependent and that it is mediated by a calpain located in the mitochondrial intermembrane space. We can now report that, in addition to a sustained intracellular Ca2+ elevation, enhanced formation of reactive oxygen species (ROS) is a prerequisite step for AIF to be cleaved and released from mitochondria in staurosporine-treated cells. These events occurred independent of the redox state of the mitochondria and were not influenced by binding of pyridine nucleotides to AIR Chelation of cytosolic Ca2+ by BAPTA/AM suppressed the elevation of both Ca2+ and ROS, suggesting that the Ca2+ rise was the most upstream signal required for AIF processing. We could further show that the stimulated ROS production leads to oxidative modification (carbonylation) of AIF, which markedly increases its rate of cleavage by calpain. Accordingly, pretreatment of the cells with antioxidants blocked AIF carbonylation, as well as its subsequent cleavage and release from the mitochondria. Combined, our data provide evidence that ROS-mediated, posttranslational modification of AIF is critical for its cleavage by calpain and thus for AIF-mediated cell death. (c) 2009 Elsevier Inc. All rights reserved.
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