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Hydrogen Peroxide Activation of ERK5 Confers Resistance to Jurkat Cells Against Apoptosis Induced by the Extrinsic Pathway

机译:ERK5的过氧化氢激活赋予Jurkat细胞抵抗外源性途径诱导的凋亡的能力。

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摘要

Reactive oxygen species (ROS) including hydrogen peroxide (H2O2) exhibit both pro-survival and pro-death signaling in leukemic cells. We examined the effect of exogenous H2O2 on Fas ligand (FasL) -induced apoptosis in Jurkat cells. H2O2 applied prior to (pre-conditioning) and during (post-conditioning) FasL stimulation attenuated early apoptosis through activation of EKR5. H2O2 increased the activated caspase-8 sequestered in the mitochondria thereby decreasing cell death through the extrinsic apoptotic pathway. In addition, inhibition of a protein tyrosine phosphatase likely explains the post-conditioning requirement for H2O2. Given that chemotherapeutic agents used for the treatment of acute lymphoblastic leukemia are thought to work partly through production of ROS, a simultaneous inhibition of the ERK5 pathway may abrogate the ROS-initiated pro-survival signaling for an enhanced cell kill.
机译:包括过氧化氢(H2O2)在内的活性氧(ROS)在白血病细胞中既表现出生存前信号,又表现出死亡前信号。我们检查了外源H2O2对Fas配体(FasL)诱导的Jurkat细胞凋亡的影响。 FasL刺激之前(预处理)和过程中(预处理)施加的H2O2通过激活EKR5减弱早期凋亡。 H2O2增加了隔离在线粒体中的活化的caspase-8,从而减少了通过外在凋亡途径的细胞死亡。另外,抑制蛋白酪氨酸磷酸酶可能解释了H2O2的后处理要求。考虑到用于治疗急性淋巴细胞白血病的化学治疗药物被认为部分通过产生ROS起作用,因此对ERK5途径的同时抑制可能会废除ROS启动的促存活信号,从而增强细胞杀伤力。

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