Author/Authors :
Yoshida، نويسنده , , Kengo and Kubo، نويسنده , , Yoshiko and Kusunoki، نويسنده , , Yoichiro and Morishita، نويسنده , , Yukari and Nagamura، نويسنده , , Hiroko and Hayashi، نويسنده , , Ikue and Kyoizumi، نويسنده , , Seishi and Seyama، نويسنده , , Toshio and Nakachi، نويسنده , , Kei and Hayashi، نويسنده , , Tomonori، نويسنده ,
Abstract :
To improve our understanding of ionizing radiation effects on immune cells, we investigated steps leading to radiation-induced cell death in MOLT-4, a thymus-derived human leukemia cell. After exposure of MOLT-4 cells to 4 Gy of X-rays, irradiated cells sequentially showed increase in intracellular reactive oxygen species (ROS), decrease in mitochondrial membrane potential, and eventually apoptotic cell death. In the presence of the caspase inhibitor z-VAD-fmk, irradiated cells exhibited necrotic characteristics such as mitochondrial swelling instead of apoptosis. ROS generation was not detected during this necrotic cell death process. These results indicate that radiation-induced apoptosis in MOLT-4 cells requires elevation of intracellular ROS as well as activation of a series of caspases, whereas the cryptic necrosis program—which is independent of intracellular ROS generation and caspase activation—is activated when the apoptosis pathway is blocked.
Keywords :
Reactive oxygen species , apoptosis , caspase , immune cells , Ionizing radiation , necrosis