Cited by 358Redox biology and oxidative stressMitochondrial Function and PathologyGlutathione Transferases and Polymorphisms

Manganese Superoxide Dismutase: Guardian of the Powerhouse

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Holley, Aaron K., Bakthavatchalu, Vasudevan, Velez-Roman, Joyce M., St. Clair, Daret K.·2011·International Journal of Molecular Sciences

Abstract

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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References 412 · Cited by 358

Research works printed but not linked: 2

  1. [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
  2. [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)
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
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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