作为对氧化应激的反应,DNA损伤反应途径调节Nrf2
Xiao-You Jiang1,2, Qi-Qiang Guo1,2, Shan-Shan Wang1,2
1The College of Basic Medical Science, Health Sciences Institute, China Medical University, Shenyang, Liaoning Province 110122, China.
Science advances
|July 25, 2025
概括
活性氧物种 (ROS) 激活DNA损伤反应 (DDR) 途径,调节Nrf2的稳定性和活性. 这种机制增强了细胞的抗氧化能力,并保护细胞免受氧化应激引起的损伤.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 核因子红色素2相关因子2 (Nrf2) 是抗氧化反应和氧化还原平衡的关键调节者.
- 将氧化应激信号转化为Nrf2激活的精确细胞机制尚未完全理解.
研究的目的:
- 阐明将氧化应激与Nrf2介导的抗氧化反应联系起来的信号通路.
- 研究DNA损伤反应 (DDR) 途径在Nrf2调控中的作用.
主要方法:
- 研究了活性氧物种 (ROS) 作为信号分子的作用.
- 利用基于细胞的测试来检查蛋白质-蛋白质相互作用和酸化事件.
- 采用了淘汰赛小鼠模型 (Chk2-/-) 和缺血/反损伤模型.
主要成果:
- ROS激活了DDR通路,特别是CHK2激酶.
- CHK2 酸化 p62,破坏 Keap1-Nrf2 相互作用并稳定 Nrf2.
- CHK2直接酸化Nrf2,增强其转录活性.
- 在氧化应激模型中,Chk2-/-小鼠表现出受损的Nrf2信号和增加的损伤.
结论:
- 在DDR路径和ROS诱导的Nrf2激活之间建立了直接联系.
- 这一途径增强了细胞抗氧化剂防御机制.
- 这些发现提供了关于细胞对氧化应激保护的关键见解.
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