活性氧
脂质过氧化
GPX4
过氧化氢
氧化应激
谷胱甘肽
程序性细胞死亡
诱导剂
细胞生物学
化学
过氧化脂质
生物物理学
生物
生物化学
细胞凋亡
酶
谷胱甘肽过氧化物酶
基因
作者
Yuting Wang,Huming Yan,Yongkang Yue,Yongbin Zhang,Fangjun Huo,Fangqin Cheng,Caixia Yin
标识
DOI:10.1016/j.cej.2023.142496
摘要
Ferroptosis is a cell death mode of lipid peroxidation caused by iron metabolism disorder and redox imbalance, which is closely associated with the evolution of tumour and ischemia reperfusion injury and other diseases, and it involves the excessive accumulation of reactive oxygen species promoting ferroptosis pathway and thiols-associated anti-ferroptosis pathway. To study the dynamic correlation between reactive oxygen species and active sulfur in the two pathways is of great significance for revealing the precise regulation mechanism of ferroptosis. Hydrogen peroxide (H2O2) and glutathione (GSH), as very active redox species in organisms, participate dynamically in the ferroptosis process. In this study, hemicyanine dye conjugated H2O2 specific response site were coupled with coumarin derivative containing GSH specific response site, realizing distinguishing simultaneous detection of H2O2 and GSH through near-infrared and cyan fluorescence emission after response. At the cellular level, the dynamic correlation between H2O2 and GSH in the ferroptosis pathway was explored, and the synergistic ferroptosis inducer was screened for further application at the tumor level, then monitoring the process of ferroptosis inducer used for tumor ablation and ferroptosis inhibitor used to alleviate kidney ischemia–reperfusion injury by fluorescence imaging.
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