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      Reactive oxygen species regulate activation-induced T cell apoptosis.

      Immunity
      Animals, Antigens, CD95, pharmacology, Apoptosis, drug effects, immunology, Caspases, metabolism, physiology, Enzyme Activation, Female, Free Radical Scavengers, Leukemia L1210, Lymphocyte Activation, Manganese, Membrane Potentials, Metalloporphyrins, Mice, Mice, Inbred C57BL, Mitochondria, Reactive Oxygen Species, Superantigens, T-Lymphocytes, Tumor Necrosis Factor-alpha

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          Abstract

          Reactive oxygen species (ROS) mediate apoptosis in a number of cell types. We studied the role that ROS play in activated T cell apoptosis by activating T cells in vivo and then culturing them for a short time. Activated T cells died independently of Fas and TNF alpha. Their death was characterized by rapid loss of mitochondrial transmembrane potential (delta psi(m)), caspase-dependent DNA fragmentation, and superoxide generation. A superoxide dismutase mimetic, Mn (III) tetrakis (5, 10, 15, 20-benzoic acid) porphyrin (MnTBAP), protected T cells from superoxide generation, caspase-dependent DNA loss, loss of delta psi(m), and cell death. These results indicate that ROS can regulate signals involved in caspase activation and apoptosis and may contribute to peripheral T cell deletion.

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