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Caspases activation in hyperthermia-induced stimulation of TRAIL apoptosis

机译:热疗诱导的TRAIL凋亡刺激中的胱天蛋白酶激活

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In leukemia cells, hyperthermia enhances tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis. The phenomenon is caspase-dependent and results in membrane changes leading to an increased recognition of TRAIL death receptors by TRAIL. Because either caspase-2 or an apical proteolytic event has been recently proposed to act as an initiator of the cell death mechanism induced by heat shock, we have investigated the hierarchy of caspase activation in cells exposed to the combined heat shock plus TRAIL treatment. We report here that caspases-2, -3, and -8 were the first caspases to be activated. As expected, caspase-8 is required and indispensable during the initiation of this death signaling. Caspase-2 may also participate in the phenomenon but, in contrast to caspase-8, its presence appears dispensable because its depletion by small interfering RNA is devoid of effects. Our observations also suggest a role of caspase-3 and of a particular cleaved form of this caspase during the early signals of heat shock plus TRAIL-induced apoptosis.
机译:在白血病细胞中,高热会增强肿瘤坏死因子相关的凋亡诱导配体(TRAIL)诱导的凋亡。该现象是胱天蛋白酶依赖性的,并导致膜改变,导致TRAIL对TRAIL死亡受体的识别增加。因为最近有人提出caspase-2或顶端蛋白水解事件起因于热休克诱导的细胞死亡机制的起因,所以我们研究了热休克加TRAIL联合治疗的细胞中caspase活化的层次。我们在这里报告,caspases-2,-3和-8是第一个被激活的caspases。正如预期的那样,在死亡信号的启动过程中,caspase-8是必需的,也是必不可少的。 Caspase-2也可能参与该现象,但是与caspase-8相比,它的存在似乎是可有可无的,因为它被小的干扰RNA消耗而没有作用。我们的观察结果还表明,在热休克加TRAIL诱导的细胞凋亡的早期信号中,caspase-3的作用以及该caspase的特定裂解形式的作用。

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