Mitophagy mediated by BNIP3 and NIX protects against ferroptosis by downregulating mitochondrial reactive oxygen species
Abstract
Mitophagy plays an important role in the maintenance of mitochondrial homeostasis and can be categorized into two types: ubiquitin-mediated and receptor-mediated pathways. During receptor-mediated mitophagy, mitophagy receptors facilitate mitophagy by tethering the isolation membrane to mitochondria. Although at least five outer mitochondrial membrane proteins have been identified as mitophagy receptors, their individual contribution and interrelationship remain unclear. Here, we show that HeLa cells lacking BNIP3 and NIX, two of the five receptors, exhibit a complete loss of mitophagy in various conditions. Conversely, cells deficient in the other three receptors show normal mitophagy. Using BNIP3/NIX double knockout (DKO) cells as a model, we reveal that mitophagy deficiency elevates mitochondrial reactive oxygen species (mtROS), which leads to activation of the Nrf2 antioxidant pathway. Notably, BNIP3/NIX DKO cells are highly sensitive to ferroptosis when Nrf2-driven antioxidant enzymes are compromised. Moreover, the sensitivity of BNIP3/NIX DKO cells is fully rescued upon the introduction of wild-type BNIP3 and NIX, but not the mutant forms incapable of facilitating mitophagy. Consequently, our results demonstrate that BNIP3 and NIX-mediated mitophagy plays a role in regulating mtROS levels and protects cells from ferroptosis.
Copyright and License
© The Author(s), under exclusive licence to ADMC Associazione Differenziamento e Morte Cellulare 2024.
Copyright and License
We thank Feng Zhang (Broad Institute of MIT and Harvard) and Eric Campeau (University of Massachusetts Medical School) for providing plasmids and CCRF (Niigata University) for supporting FACS analysis.
Funding
This work was supported in part by the Japan Society for the Promotion of Science KAKENHI grants (16KK0162 and 22K07207 to SY and 19H05712, 18H04858, and 18H04691, to TK), AMED grant (JP21gm6110013, JP23ek0109647 and JP23gm1710006 to TK), and the Takeda Science Foundation (to SY).
Contributions
SY, YS, and TK designed the experiments. SY generated receptor KO cell lines using the CRIPSR/Cas9 genome editing system. SY performed all cellular analyses. YS, YM, and RM performed the metabolomic analysis. SY, KI, KF, TF, DCC, and TK wrote the manuscript.
Data Availability
All relevant data are available from the authors. Original immunoblot data are provided in the Supplemental Material.
Conflict of Interest
The authors declare no competing interests.
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Additional details
- ISSN
- 1476-5403
- PMCID
- PMC11094013
- Japan Society for the Promotion of Science
- 16KK0162
- Japan Society for the Promotion of Science
- 22K07207
- Japan Society for the Promotion of Science
- 19H05712
- Japan Society for the Promotion of Science
- 18H04858
- Japan Society for the Promotion of Science
- 18H04691
- Japan Agency for Medical Research and Development
- JP21gm6110013
- Japan Agency for Medical Research and Development
- JP23ek0109647
- Japan Agency for Medical Research and Development
- JP23gm1710006
- Takeda Science Foundation
- Caltech groups
- Division of Biology and Biological Engineering, Tianqiao and Chrissy Chen Institute for Neuroscience