Abstract

Through their many and varied metabolic functions, mitochondria power life. Paradoxically, mitochondria also have a central role in apoptotic cell death. Upon induction of mitochondrial apoptosis, mitochondrial outer membrane permeabilization (MOMP) usually commits a cell to die. Apoptotic signalling downstream of MOMP involves cytochrome c release from mitochondria and subsequent caspase activation. As such, targeting MOMP in order to manipulate cell death holds tremendous therapeutic potential across different diseases, including neurodegenerative diseases, autoimmune disorders and cancer. In this Review, we discuss new insights into how mitochondria regulate apoptotic cell death. Surprisingly, recent data demonstrate that besides eliciting caspase activation, MOMP engages various pro-inflammatory signalling functions. As we highlight, together with new findings demonstrating cell survival following MOMP, this pro-inflammatory role suggests that mitochondria-derived signalling downstream of pro-apoptotic cues may also have non-lethal functions. Finally, we discuss the importance and roles of mitochondria in other forms of regulated cell death, including necroptosis, ferroptosis and pyroptosis. Collectively, these new findings offer exciting, unexplored opportunities to target mitochondrial regulation of cell death for clinical benefit.

Keywords

MitochondrionProgrammed cell deathCell biologyPyroptosisNecroptosisBiologyApoptosisCellCaspaseIntrinsic apoptosisBiochemistry

MeSH Terms

AnimalsApoptosisCaspasesCytochromes cHumansMitochondriaMitochondrial MembranesSignal Transduction

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Publication Info

Year
2019
Type
review
Volume
21
Issue
2
Pages
85-100
Citations
2214
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

2214
OpenAlex
37
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Cite This

Florian J. Bock, Stephen W. G. Tait (2019). Mitochondria as multifaceted regulators of cell death. Nature Reviews Molecular Cell Biology , 21 (2) , 85-100. https://doi.org/10.1038/s41580-019-0173-8

Identifiers

DOI
10.1038/s41580-019-0173-8
PMID
31636403

Data Quality

Data completeness: 81%