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肿瘤坏死因子-α诱导的信号转导和细胞死亡中的活性氧。

Reactive oxygen species in TNFalpha-induced signaling and cell death.

机构信息

Cell and Cancer Biology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health (NIH), Bethesda, MD 20892, USA.

出版信息

Mol Cells. 2010 Jul;30(1):1-12. doi: 10.1007/s10059-010-0105-0. Epub 2010 Jul 14.

Abstract

TNFalpha is a pleotropic cytokine that initiates many downstream signaling pathways, including NF-kappaB activation, MAP kinase activation and the induction of both apoptosis and necrosis. TNFalpha has shown to lead to reactive oxygen species generation through activation of NADPH oxidase, through mitochondrial pathways, or other enzymes. As discussed, ROS play a role in potentiation or inhibition of many of these signaling pathways. We particularly discuss the role of sustained JNK activation potentiated by ROS, which generally is supportive of apoptosis and "necrotic cell death" through various mechanisms, while ROS could have inhibitory or stimulatory roles in NF-kappaB signaling.

摘要

肿瘤坏死因子-α(TNFalpha)是一种多效细胞因子,可启动许多下游信号通路,包括 NF-κB 激活、MAP 激酶激活以及凋亡和坏死的诱导。TNFalpha 已被证明通过激活 NADPH 氧化酶、通过线粒体途径或其他酶来导致活性氧(ROS)的产生。如前所述,ROS 在增强或抑制许多这些信号通路中起作用。我们特别讨论了 ROS 增强的持续 JNK 激活的作用,ROS 通常通过各种机制支持凋亡和“坏死性细胞死亡”,而 ROS 在 NF-κB 信号中可能具有抑制或刺激作用。

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