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NF-E2 对 Nrf2 的支配促进 ROS 积累和巨核细胞成熟。

NF-E2 domination over Nrf2 promotes ROS accumulation and megakaryocytic maturation.

机构信息

Center for Radioisotope Sciences, Tohoku University Graduate School of Medicine, 2-1 Seiryo-cho, Aoba-ku, Sendai 980-8575, Japan.

出版信息

Blood. 2010 Jan 21;115(3):677-86. doi: 10.1182/blood-2009-05-223107. Epub 2009 Nov 9.

Abstract

In megakaryocytes, the maturation process and oxidative stress response appear to be closely related. It has been suggested that increased oxygen tension and reactive oxygen species (ROS) promote megakaryopoiesis and that the expression of stress-responsive genes responsible for ROS elimination declines during megakaryocytic maturation. NF-E2 p45 is an essential regulator of megakaryopoiesis, whereas Nrf2 is a key activator of stress-responsive genes. Because p45 and Nrf2 have similar DNA-binding specificities, we hypothesized that p45 competes with Nrf2 to repress stress-responsive genes and achieves favorable intracellular conditions to allow ROS to be efficiently used as signaling molecules. We conducted comprehensive gene expression profiling with wild-type and p45-null megakaryocytes and examined the functional relationship between p45 and Nrf2. We found that 2 characteristic gene clusters are defined within p45 target genes: platelet genes and cytoprotective genes. The former are unique targets activated by p45, whereas the latter are common targets of p45 and Nrf2. Further analysis suggested that, as a less efficacious activator, p45 maintains moderate expression of cytoprotective genes through competing with Nrf2 and promotes ROS accumulation. Increased ROS enhanced platelet gene expression. These results suggest that p45 dominates over Nrf2 to enhance megakaryocytic maturation by promoting ROS accumulation.

摘要

在巨核细胞中,成熟过程和氧化应激反应似乎密切相关。有人提出,氧张力和活性氧(ROS)的增加促进巨核细胞生成,而负责 ROS 清除的应激反应基因的表达在巨核细胞成熟过程中下降。NF-E2 p45 是巨核细胞生成的必需调节剂,而 Nrf2 是应激反应基因的关键激活剂。由于 p45 和 Nrf2 具有相似的 DNA 结合特异性,我们假设 p45 与 Nrf2 竞争,抑制应激反应基因,并实现有利的细胞内条件,使 ROS 能够有效地用作信号分子。我们对野生型和 p45 缺失的巨核细胞进行了全面的基因表达谱分析,并研究了 p45 和 Nrf2 之间的功能关系。我们发现,p45 靶基因中存在 2 个特征性基因簇:血小板基因和细胞保护基因。前者是 p45 激活的特有靶点,而后者是 p45 和 Nrf2 的共同靶点。进一步的分析表明,作为一种效力较低的激活剂,p45 通过与 Nrf2 竞争来维持细胞保护基因的适度表达,并促进 ROS 积累。增加的 ROS 增强了血小板基因的表达。这些结果表明,p45 通过促进 ROS 积累而主导 Nrf2,从而增强巨核细胞成熟。

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