Mitochondrial Regulation of Cell-Death

Author(s):  
Richard Jäger ◽  
Howard O. Fearnhead
Autophagy ◽  
2011 ◽  
Vol 7 (7) ◽  
pp. 793-794 ◽  
Author(s):  
Elizabeth A. Tanner ◽  
Kim McCall

2021 ◽  
Vol 220 (9) ◽  
Author(s):  
Boyi Gan

Ferroptosis is a form of iron-dependent regulated cell death driven by uncontrolled lipid peroxidation. Mitochondria are double-membrane organelles that have essential roles in energy production, cellular metabolism, and cell death regulation. However, their role in ferroptosis has been unclear and somewhat controversial. In this Perspective, I summarize the diverse metabolic processes in mitochondria that actively drive ferroptosis, discuss recently discovered mitochondria-localized defense systems that detoxify mitochondrial lipid peroxides and protect against ferroptosis, present new evidence for the roles of mitochondria in regulating ferroptosis, and outline outstanding questions on this fascinating topic for future investigations. An in-depth understanding of mitochondria functions in ferroptosis will have important implications for both fundamental cell biology and disease treatment.


1999 ◽  
Vol 19 (5) ◽  
pp. 3842-3847 ◽  
Author(s):  
Atsushi Suzuki ◽  
Yumi Tsutomi ◽  
Naoe Yamamoto ◽  
Tomoko Shibutani ◽  
Kouichi Akahane

ABSTRACT Death receptor Fas transduces cell death signaling upon stimulation by Fas ligand, and this death signaling is mediated by caspase. Recently, we reported that the cell cycle regulator p21 interacts with procaspase 3 to resist Fas-mediated cell death. In the present study, the molecular characterization and functional region of the procaspase 3-p21 complex was further investigated. We observed the p21 expression in the mitochondrial fraction of HepG2 cells and detected Fas-mediated cell death only in the presence of actinomycin D. However, mitochondrial-DNA-lacking HepG2 (MDLH) cells showed this effect even in the absence of actinomycin D. Both p21 and procaspase 3 were expressed in MDLH cells, but the procaspase 3-p21 complex formation was not observed. Interestingly, the resistance to Fas-mediated cell death in the MDLH cells without actinomycin D was recovered after microinjection of HepG2-derived mitochondria into the MDLH cells. We conclude that mitochondria are necessary for procaspase 3-p21 complex formation and propose that the mitochondrial role during cell death is not only death induction but also death suppression.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Adam Z. Spitz ◽  
Emmanouil Zacharioudakis ◽  
Denis E. Reyna ◽  
Thomas P. Garner ◽  
Evripidis Gavathiotis

AbstractThe BCL-2 family protein BAX has essential activity in mitochondrial regulation of cell death. While BAX activity ensures tissue homeostasis, when dysregulated it contributes to aberrant cell death in several diseases. During cellular stress BAX is transformed from an inactive cytosolic conformation to a toxic mitochondrial oligomer. Although the BAX transformation process is not well understood, drugs that interfere with this process are useful research tools and potential therapeutics. Here, we show that Eltrombopag,  an FDA-approved drug,  is a direct inhibitor of BAX. Eltrombopag binds the BAX trigger site distinctly from BAX activators, preventing them from triggering BAX conformational transformation and simultaneously promoting stabilization of the inactive BAX structure. Accordingly, Eltrombopag is capable of inhibiting BAX-mediated apoptosis induced by cytotoxic stimuli. Our data demonstrate structure-function insights into a mechanism of BAX inhibition and reveal a mechanism for Eltrombopag that may expand its use in diseases of uncontrolled cell death.


2013 ◽  
Vol 5 (9) ◽  
pp. a008706-a008706 ◽  
Author(s):  
S. W. G. Tait ◽  
D. R. Green

2016 ◽  
Vol 3 (3) ◽  
pp. 101-108 ◽  
Author(s):  
Lorenzo Galluzzi ◽  
Oliver Kepp ◽  
Guido Kroemer

2006 ◽  
Vol 163 (1-2) ◽  
pp. 4-14 ◽  
Author(s):  
Vladimir Gogvadze ◽  
Sten Orrenius

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