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

Authors :
Chen X
Tsvetkov AS
Shen HM
Isidoro C
Ktistakis NT
Linkermann A
Koopman WJH
Simon HU
Galluzzi L
Luo S
Xu D
Gu W
Peulen O
Cai Q
Rubinsztein DC
Chi JT
Zhang DD
Li C
Toyokuni S
Liu J
Roh JL
Dai E
Juhasz G
Liu W
Zhang J
Yang M
Liu J
Zhu LQ
Zou W
Piacentini M
Ding WX
Yue Z
Xie Y
Petersen M
Gewirtz DA
Mandell MA
Chu CT
Sinha D
Eftekharpour E
Zhivotovsky B
Besteiro S
Gabrilovich DI
Kim DH
Kagan VE
Bayir H
Chen GC
Ayton S
Lünemann JD
Komatsu M
Krautwald S
Loos B
Baehrecke EH
Wang J
Lane JD
Sadoshima J
Yang WS
Gao M
Münz C
Thumm M
Kampmann M
Yu D
Lipinski MM
Jones JW
Jiang X
Zeh HJ
Kang R
Klionsky DJ
Kroemer G
Tang D
Source :
Autophagy [Autophagy] 2024 Jun; Vol. 20 (6), pp. 1213-1246. Date of Electronic Publication: 2024 Mar 24.
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.

Details

Language :
English
ISSN :
1554-8635
Volume :
20
Issue :
6
Database :
MEDLINE
Journal :
Autophagy
Publication Type :
Academic Journal
Accession number :
38442890
Full Text :
https://doi.org/10.1080/15548627.2024.2319901