粒体自噬
生物
细胞生物学
品脱1
自噬
线粒体
逆行信号
功能(生物学)
帕金
自噬体
信号转导
活性氧
磷酸化
细胞信号
贝肯1
调节器
DNA损伤
死孢子体1
机制(生物学)
信号
线粒体ROS
核心
线粒体融合
平衡
作者
Qiqiang Guo,Qi-Qiang Guo,Xiaoyu Song,Xiaoyu Song,Liu Cao
出处
期刊:Autophagy
[Taylor & Francis]
日期:2025-11-19
卷期号:22 (2): 434-435
标识
DOI:10.1080/15548627.2025.2592883
摘要
Mitochondrial reactive oxygen species (mtROS) are typically viewed as harmful byproducts of stress. However, our recent study establishes their fundamental role as essential signaling molecules that activate a protective adaptive response. We discovered that mtROS serve as the specific trigger to activate the ATM-CHEK2/CHK2 DNA damage response pathway, which in turn coordinates the key steps of PINK1-PRKN/Parkin-dependent mitophagy. Upon activation by mtROS, CHEK2 phosphorylates ATAD3A to initiate PINK1 import arrest, OPTN to enhance cargo recognition, and BECN1 (beclin 1) to promote autophagosome formation. This work reveals a novel mtROS-driven signaling cascade, expanding the function of the ATM-CHEK2 pathway beyond the nucleus and positioning it as a central integrator of cellular homeostasis by responding to both genomic and mitochondrial stress.
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