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Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome

Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell dea...

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Published in:Journal of cellular physiology 2020-10, Vol.235 (10), p.6767-6778
Main Authors: Lee, Young‐Sun, Kalimuthu, Kalishwaralal, Seok Park, Yong, Makala, Hima, Watkins, Simon C., Choudry, M. Haroon A., Bartlett, David L., Tae Kwon, Yong, Lee, Yong J.
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creator Lee, Young‐Sun
Kalimuthu, Kalishwaralal
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Lee, Yong J.
description Ferroptosis has been reported as a unique form of cell death. However, in recent years, researchers have increasingly challenged the uniqueness of ferroptosis compared to other types of cell death. In this study, we examined whether ferroptosis shares cell death pathways with other types of cell death, especially autophagy, via the autophagic process. Here, we observed that ferroptosis inducers (artesunate [ART] and erastin [ERA]) and autophagy inducers (bortezomib [BOR] and XIE62‐1004) led to autophagosome formation via the endoplasmic reticulum (ER) stress response. Unlike XIE62‐1004, ART, ERA, and BOR, which affect glutathione production or utilization, induced oxidative stress responses—an increase in the levels of heme oxygenase‐1 and lipid peroxidation. Oxidative stress responses were attenuated by deletion of autophagy‐related gene‐5 or treatment with autophagy inhibitors (bafilomycin and chloroquine). Our studies provide an overview of common death pathways—the ER stress response‐associated autophagic process in ferroptosis and autophagy. We also highlight the role played by glutathione redox system in the outcome of the autophagic process. The role played by glutathione redox system in the outcome of the autophagic process.
doi_str_mv 10.1002/jcp.29571
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subjects Apoptosis
Apoptosis - physiology
Artesunate
Autophagosomes - metabolism
Autophagosomes - physiology
Autophagy
Autophagy - physiology
Bortezomib
Cell death
Cell Line, Tumor
Cellular stress response
Chloroquine
Endoplasmic reticulum
endoplasmic reticulum stress
Endoplasmic Reticulum Stress - physiology
Ferroptosis
Ferroptosis - physiology
Gene deletion
Glutathione
Glutathione - metabolism
HCT116 Cells
Heme
Heme Oxygenase-1 - metabolism
Humans
Lipid peroxidation
Lipid Peroxidation - physiology
Lipids
Mortality
Oxidation-Reduction
Oxidative stress
Oxidative Stress - physiology
Oxygenase
Peroxidation
Phagocytosis
Signal Transduction - physiology
title Ferroptotic agent‐induced endoplasmic reticulum stress response plays a pivotal role in the autophagic process outcome
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