Back to Search Start Over

International consensus guidelines for the definition, detection, and interpretation of autophagy-dependent ferroptosis.

Authors :
Chen, Xin
Tsvetkov, Andrey S.
Shen, Han-Ming
Isidoro, Ciro
Ktistakis, Nicholas T.
Linkermann, Andreas
Koopman, Werner J.H.
Simon, Hans-Uwe
Galluzzi, Lorenzo
Luo, Shouqing
Xu, Daqian
Gu, Wei
Peulen, Olivier
Cai, Qian
Rubinsztein, David C.
Chi, Jen-Tsan
Zhang, Donna D.
Li, Changfeng
Toyokuni, Shinya
Liu, Jinbao
Source :
Autophagy; Jun2024, Vol. 20 Issue 6, p1213-1246, 34p
Publication Year :
2024

Abstract

Macroautophagy/autophagy is a complex degradation process with a dual role in cell death that is influenced by the cell types that are involved and the stressors they are exposed to. Ferroptosis is an iron-dependent oxidative form of cell death characterized by unrestricted lipid peroxidation in the context of heterogeneous and plastic mechanisms. Recent studies have shed light on the involvement of specific types of autophagy (e.g. ferritinophagy, lipophagy, and clockophagy) in initiating or executing ferroptotic cell death through the selective degradation of anti-injury proteins or organelles. Conversely, other forms of selective autophagy (e.g. reticulophagy and lysophagy) enhance the cellular defense against ferroptotic damage. Dysregulated autophagy-dependent ferroptosis has implications for a diverse range of pathological conditions. This review aims to present an updated definition of autophagy-dependent ferroptosis, discuss influential substrates and receptors, outline experimental methods, and propose guidelines for interpreting the results. Abbreviation: 3-MA:3-methyladenine; 4HNE: 4-hydroxynonenal; ACD: accidentalcell death; ADF: autophagy-dependentferroptosis; ARE: antioxidant response element; BH2:dihydrobiopterin; BH4: tetrahydrobiopterin; BMDMs: bonemarrow-derived macrophages; CMA: chaperone-mediated autophagy; CQ:chloroquine; DAMPs: danger/damage-associated molecular patterns; EMT,epithelial-mesenchymal transition; EPR: electronparamagnetic resonance; ER, endoplasmic reticulum; FRET: Försterresonance energy transfer; GFP: green fluorescent protein;GSH: glutathione;IF: immunofluorescence; IHC: immunohistochemistry; IOP, intraocularpressure; IRI: ischemia-reperfusion injury; LAA: linoleamide alkyne;MDA: malondialdehyde; PGSK: Phen Green™ SK;RCD: regulatedcell death; PUFAs: polyunsaturated fatty acids; RFP: red fluorescentprotein;ROS: reactive oxygen species; TBA: thiobarbituricacid; TBARS: thiobarbituric acid reactive substances; TEM:transmission electron microscopy. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15548627
Volume :
20
Issue :
6
Database :
Complementary Index
Journal :
Autophagy
Publication Type :
Academic Journal
Accession number :
178134512
Full Text :
https://doi.org/10.1080/15548627.2024.2319901