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首页> 外文期刊>FEBS letters. >ROS leads to MnSOD upregulation through ERK2 translocation and p53 activation in selenite-induced apoptosis of NB4 cells.
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ROS leads to MnSOD upregulation through ERK2 translocation and p53 activation in selenite-induced apoptosis of NB4 cells.

机译:ROS通过亚硒酸盐诱导的NB4细胞凋亡通过ERK2易位和p53激活导致MnSOD上调。

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摘要

Following our previous finding that sodium selenite induces apoptosis in human leukemia NB4 cells, we now show that the expression of the critical antioxidant enzyme manganese superoxide dismutase (MnSOD) is remarkably elevated during this process. We further reveal that reactive oxygen species (ROS), especially superoxide radicals, play a crucial role in selenite-induced MnSOD upregulation, with extracellular regulated kinase (ERK) and p53 closely implicated. Specifically, ERK2 translocates into the nucleus driven by ROS, where it directly phosphorylates p53, leading to dissociation of p53 from its inhibitory protein mouse double minute 2 (MDM2). Active p53 directly mediates the expression of MnSOD, serving as the link between ERK2 translocation and MnSOD upregulation.
机译:根据我们先前的发现,亚硒酸钠可诱导人白血病NB4细胞凋亡,我们现在显示在此过程中,重要的抗氧化酶锰超氧化物歧化酶(MnSOD)的表达显着提高。我们进一步揭示,活性氧(ROS),尤其是超氧自由基,在亚硒酸盐诱导的MnSOD上调中起关键作用,与细胞外调节激酶(ERK)和p53密切相关。具体而言,ERK2易位到由ROS驱动的核中,在那里它直接使p53磷酸化,从而导致p53从其抑制性蛋白小鼠doubleminute 2(MDM2)分离。活性p53直接介导MnSOD的表达,作为ERK2易位与MnSOD上调之间的联系。

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