Journal
MOLECULAR AND CELLULAR BIOLOGY
Volume 27, Issue 10, Pages 3625-3639Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.02295-06
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Reactive oxygen species (ROS) play a key role in regulation of activation-induced T-cell death (AICD) by induction of CD95L expression. However, the molecular source and the signaling steps necessary for ROS production are largely unknown. Here, we show that the proximal T-cell receptor-signaling machinery, including ZAP70 (zeta chain-associated protein kinase 70), IAT (linker of activated T cells), SLP76 (SH2 domain-containing leukocyte protein of 76 kDa), PLC gamma 1 (phospholipase C gamma 1), and PKC theta (protein kinase C theta), are crucial for ROS production. PKC theta is translocated to the mitochondria. By using cells depleted of mitochondrial DNA, we identified the mitochondria as the source of activation-induced ROS. Inhibition of mitochondrial electron transport complex I assembly by small interfering RNA (siRNA) -mediated knockdown of the chaperone NDUFAF1 resulted in a block of ROS production. Complex I-derived ROS are converted into a hydrogen peroxide signal by the mitochondrial superoxide dismutase. This signal is essential for CD95L expression, as inhibition of complex I assembly by NDUFAF1-specific siRNA prevents AICD. Similar results were obtained when metformin, an antidiabetic drug and mild complex I inhibitor, was used. Thus, we demonstrate for the first time that PKC theta-dependent ROS generation by mitochondrial complex I is essential for AICD.
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