Identification of essential sites of lipid peroxidation in ferroptosis

被引:0
|
作者
A. Nikolai von Krusenstiern
Ryan N. Robson
Naixin Qian
Baiyu Qiu
Fanghao Hu
Eduard Reznik
Nailah Smith
Fereshteh Zandkarimi
Verna M. Estes
Marcel Dupont
Tal Hirschhorn
Mikhail S. Shchepinov
Wei Min
K. A. Woerpel
Brent R. Stockwell
机构
[1] Columbia University,Department of Biological Sciences
[2] New York University,Department of Chemistry
[3] Columbia University,Department of Chemistry
[4] Retrotope,undefined
[5] Inc.,undefined
来源
Nature Chemical Biology | 2023年 / 19卷
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摘要
Ferroptosis, an iron-dependent form of cell death driven by lipid peroxidation, provides a potential treatment avenue for drug-resistant cancers and may play a role in the pathology of some degenerative diseases. Identifying the subcellular membranes essential for ferroptosis and the sequence of their peroxidation will illuminate drug discovery strategies and ferroptosis-relevant disease mechanisms. In this study, we employed fluorescence and stimulated Raman scattering imaging to examine the structure–activity–distribution relationship of ferroptosis-modulating compounds. We found that, although lipid peroxidation in various subcellular membranes can induce ferroptosis, the endoplasmic reticulum (ER) membrane is a key site of lipid peroxidation. Our results suggest an ordered progression model of membrane peroxidation during ferroptosis that accumulates initially in the ER membrane and later in the plasma membrane. Thus, the design of ER-targeted inhibitors and inducers of ferroptosis may be used to optimally control the dynamics of lipid peroxidation in cells undergoing ferroptosis.
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页码:719 / 730
页数:11
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