Manganese Superoxide Dismutase: Guardian of the Powerhouse
Open accessAbstract
The mitochondrion is vital for many metabolic pathways in the cell, contributing all or important constituent enzymes for diverse functions such as β-oxidation of fatty acids, the urea cycle, the citric acid cycle, and ATP synthesis. The mitochondrion is also a major site of reactive oxygen species (ROS) production in the cell. Aberrant production of mitochondrial ROS can have dramatic effects on cellular function, in part, due to oxidative modification of key metabolic proteins localized in the mitochondrion. The cell is equipped with myriad antioxidant enzyme systems to combat deleterious ROS production in mitochondria, with the mitochondrial antioxidant enzyme manganese superoxide dismutase (MnSOD) acting as the chief ROS scavenging enzyme in the cell. Factors that affect the expression and/or the activity of MnSOD, resulting in diminished antioxidant capacity of the cell, can have extraordinary consequences on the overall health of the cell by altering mitochondrial metabolic function, leading to the development and progression of numerous diseases. A better understanding of the mechanisms by which MnSOD protects cells from the harmful effects of overproduction of ROS, in particular, the effects of ROS on mitochondrial metabolic enzymes, may contribute to the development of novel treatments for various diseases in which ROS are an important component.
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MnSOD catalyzes the conversion of superoxide radical anion into H2O2 and O2.
“MnSOD catalyzes the conversion of superoxide radical anion into H2O2 and O2 [81,82,83]”
From Mitochondrial Oxidative and Nitrosative Stress and Alzheimer Disease (2020) · cites this paper as [81]
MnSOD is the main ROS scavenger in the inner mitochondrial matrix and acts as the first line of defense against mitochondrial oxidative damage.
“MnSOD is the main ROS scavenger in the inner mitochondrial matrix, and acts as the first line of defense against mitochondrial oxidative damage (Holley et al., 2011).”
From mTOR inhibition prevents epithelial stem cell senescence and protects from radiation-induced mucositis (2012) · cites this paper as Holley et al., 2011
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References 412 · Cited by 358
Research works printed but not linked: 2
- [390]Eldridge A Fan M Candas D Chromy B Li JJ Profiling of MnSOD Interaction Proteins in Low-Dose Radiation Induced Adaptive Response Proceedings of the Low Dose Radiation Research Investigators’ Workshop Washington, DC, USA 9–11 May 2011
- [391]Jin C Fan M Liu R Nantajit D Candas D Vaughan ATM Murley JS Woloschak G Grdina DJ Li JJ Cyclin D1 and CDK4 Translocate into Mitochondria and Interact with MnSOD in Low-Dose Radiation-Induced Adaptive Radioprotection Proceedings of the Low Dose Radiation Research Investigators’ Workshop Washington, DC, USA 9–11 May 2011
- Authors
- Holley, A. K., Bakthavatchalu, V., Velez-Roman, J. M., & St. Clair, D. K.
- Affiliations
- University of Kentucky (US)
- Graduate Center for Toxicology, University of Kentucky, 454 HSRB, 1095 VA Drive, Lexington, KY 40536, USA
- Venue
- International Journal of Molecular Sciences
- Publisher
- MDPI AG
- Published
- 2011-10-21
- Volume
- 12
- Issue
- 10
- Pages
- 7114-7162
- ISSN
- 1422-0067 (ISSN-L)
- PMC
- PMC3211030
- OpenAlex
- W2014175688
- Cited by
- 358
- References
- 412
- Citations by year
- 2026: 34 · 2025: 38 · 2024: 36 · 2023: 31 · 2022: 34 · 2021: 40 · 2020: 27 · 2019: 18 · 2018: 17 · 2017: 12 · 2016: 10 · 2015: 12 · 2014: 11 · 2013: 24 · 2012: 14
- FWCI
- 1.42
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- International Journal of Molecular Sciences (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- UKnowledge (University of Kentucky) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health
- National Cancer Institute (R01CA073599, 3R01CA73599-05S1)
- National Institute of Environmental Health Sciences (T32ES007266)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
- Keywords
- manganese superoxide dismutase, mitochondria, reactive oxygen species, oxidative stress, mitochondrial metabolism, antioxidant enzymes, mitochondrial dysfunction, disease
- MeSH terms
- Superoxide Dismutase 2, Animals, Cardiovascular Diseases, Humans, Immunity, Innate, Metabolic Diseases, Mitochondria, Neoplasms, Nervous System Diseases, Superoxide Dismutase, Reactive Oxygen Species, Oxidative Stress, Electron Transport Chain Complex Proteins
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