粒体自噬
活性氧
线粒体
细胞生物学
线粒体ROS
自噬
生物
细胞内
品脱1
平衡
程序性细胞死亡
氧化应激
细胞
生物化学
细胞凋亡
作者
Akbar Zeb,Vinay Choubey,Ruby Gupta,Vladimir Veksler,Allen Kaasik
出处
期刊:Autophagy
[Taylor & Francis]
日期:2022-01-28
卷期号:18 (9): 2249-2251
被引量:3
标识
DOI:10.1080/15548627.2021.2024702
摘要
If cellular reactive oxygen species (ROS) production surpasses the intracellular antioxidant capacity, thus altering the ROS homeostasis, the cell needs to eradicate faulty mitochondria responsible for these excessive ROS. We have shown that even moderate ROS production breaks the KEAP1-PGAM5 complex, inhibiting the proteasomal removal of PGAM5. This leads to an accumulation of PGAM5 interfering with PINK1 processing that sensitizes mitochondria to autophagic removal. We propose that such a negative feedback system maintains cell ROS homeostasis.
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