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Role for Mitochondrial Oxidants as Regulators of Cellular Metabolism
Open accessAbstract
Leakage of mitochondrial oxidants contributes to a variety of harmful conditions ranging from neurodegenerative diseases to cellular senescence. We describe here, however, a physiological and heretofore unrecognized role for mitochondrial oxidant release. Mitochondrial metabolism of pyruvate is demonstrated to activate the c-Jun N-terminal kinase (JNK). This metabolite-induced rise in cytosolic JNK1 activity is shown to be triggered by increased release of mitochondrial H(2)O(2). We further demonstrate that in turn, the redox-dependent activation of JNK1 feeds back and inhibits the activity of the metabolic enzymes glycogen synthase kinase 3beta and glycogen synthase. As such, these results demonstrate a novel metabolic regulatory pathway activated by mitochondrial oxidants. In addition, they suggest that although chronic oxidant production may have deleterious effects, mitochondrial oxidants can also function acutely as signaling molecules to provide communication between the mitochondria and the cytosol.
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“The impairment of mitochondrial ETC activity in mitochondrial metabolism leads to an increase of reactive oxygen species (ROS) production which occurs mainly at Complex I and Complex III [31].”
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Cites
Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage
Nishikawa, T., Edelstein, D., Du, X. L., Yamagishi, S.-I., Matsumura, T., Kaneda, Y., Yorek, M. A., Beebe, D., Oates, P. J., Hammes, H.-P., et al. (2000) · Nature · doi:10.1038/35008121 · Cited by 4,277
The Free Radical Theory of Aging Matures
BECKMAN, K. B., & AMES, B. N. (1998) · Physiological Reviews · doi:10.1152/physrev.1998.78.2.547 · Cited by 3,879
Oxidative Stress, Caloric Restriction, and Aging
Sohal, R. S., & Weindruch, R. H. (1996) · Science · doi:10.1126/science.273.5271.59 · Cited by 3,133
Angiotensin II stimulates NADH and NADPH oxidase activity in cultured vascular smooth muscle cells.
Griendling, K. K., Minieri, C. A., Ollerenshaw, J. D., & Alexander, R. W. (1994) · Circulation Research · doi:10.1161/01.res.74.6.1141 · Cited by 2,735
Boveris, A., & Chance, B. (1973) · Biochemical Journal · doi:10.1042/bj1340707 · Cited by 2,626
Requirement for Generation of H 2 O 2 for Platelet-Derived Growth Factor Signal Transduction
Sundaresan, M., Yu, Z.-X., Ferrans, V. J., Irani, K., & Finkel, T. (1995) · Science · doi:10.1126/science.270.5234.296 · Cited by 2,520
Self-citationMitogenic Signaling Mediated by Oxidants in Ras-Transformed Fibroblasts
Irani, K., Xia, Y., Zweier, J. L., Sollott, S. J., Der, C. J., Fearon, E. R., Sundaresan, M., Finkel, T., & Goldschmidt-Clermont, P. J. (1997) · Science · doi:10.1126/science.275.5306.1649 · Cited by 1,588
Self-citationCell transformation by the superoxide-generating oxidase Mox1
Suh, Y.-A., Arnold, R. S., Lassegue, B., Shi, J., Xu, X., Sorescu, D., Chung, A. B., Griendling, K. K., & Lambeth, J. D. (1999) · Nature · doi:10.1038/43459 · Cited by 1,480
Epidermal Growth Factor (EGF)-induced Generation of Hydrogen Peroxide
Bae, Y. S., Kang, S. W., Seo, M. S., Baines, I., Tekle, E., Chock, P. B., & Rhee, S. G. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.1.217 · Cited by 1,208
Finkel, T. (1998) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(98)80147-6 · Cited by 1,170
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- Haring H., 1995, Herz, 20, 5
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Tata, D. B., & Waynant, R. W. (2008) · Proceedings of SPIE, the International Society for Optical Engineering/Proceedings of SPIE · doi:10.1117/12.763526 · Cited by 7
Reactive Oxygen Species and Antioxidants in Pancreatic β-Cell Function – Yin and Yang
Pi, J., Zhang, Q., & Andersen, M. E. (2014) · Springer eBooks · doi:10.1007/978-3-642-30018-9_159 · Cited by 7
Li, W., Shi, Y., Yang, R., Cui, J., Xiao, Y., & Le, G. (2010) · Free Radical Research · doi:10.3109/10715761003713549 · Cited by 6
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Brookes, P. S. (2007) · Springer eBooks · doi:10.1007/978-0-387-30411-3_19 · Cited by 7
Gao, Q., Hägglund, P., Gamon, L. F., & Davies, M. J. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.09.024 · Cited by 5
Yang, E. S., Huh, Y. J., & Park, J. (2013) · PubMed · Cited by 6
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Purves-Tyson, T. D., & Tomlinson, D. R. (2002) · International review of neurobiology · doi:10.1016/s0074-7742(02)50074-x · Cited by 6
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Sack, M. N. (2006) · Circulation · doi:10.1161/circulationaha.106.653485 · Cited by 6
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Gorenne, I., & Bennett, M. R. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-602-3_10 · Cited by 5
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Rashidi, A., Kirkwood, T. B. L., & Shanley, D. P. (2009) · Springer eBooks · doi:10.1007/978-3-642-00952-5_6 · Cited by 5
Globus, R. K., Caiozzo, V. J., Acharya, M. M., Fike, J. R., & Limoli, C. L. (2011) · Humana Press eBooks · doi:10.1007/978-1-61779-397-4_9 · Cited by 5
Rosenson-Schloss, R. S., Chnari, E., Brieva, T., Dang, A., & Moghe, P. (2005) · Experimental biology and medicine · doi:10.1177/153537020523000105 · Cited by 7
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Dandekar, M. P., Guin, S., Sammeta, S. S., Saha, C., Bhalerao, H. A., & Sonti, R. (2025) · Journal of Ayurveda and Integrative Medicine · doi:10.1016/j.jaim.2025.101131 · Cited by 4
Wu, Y. N., Sudarshan, V. K., Zhu, S., Shao, Y., Kim, S. J., & Zhang, Y. H. (2020) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s00424-020-02458-2 · Cited by 4
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Hawrylyshyn, K., Yin, H. R., O’Neil, C. H., Watson, A., & Pickering, J. G. (2015) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2015.07.477 · Cited by 4
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Liang, L. (2007) · OhioLink ETD Center (Ohio Library and Information Network) · Cited by 2
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Metadata
- Authors
- Nemoto, S., Takeda, K., Yu, Z.-X., Ferrans, V. J., & Finkel, T.
- Affiliations
- National Institutes of Health (US)
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 2000-10-15
- Volume
- 20
- Issue
- 19
- Pages
- 7311-7318
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC86285
- OpenAlex
- W2123273404
- Cited by
- 393
- References
- 42
- Citations by year
- 2026: 1 · 2025: 5 · 2024: 6 · 2023: 9 · 2022: 9 · 2021: 15 · 2020: 12 · 2019: 21 · 2018: 12 · 2017: 12 · 2016: 17 · 2015: 18 · 2014: 17 · 2013: 10 · 2012: 19
- FWCI
- 5.66
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Molecular and Cellular Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- hydrogen peroxide, c-Jun N-terminal kinase, JNK1, glycogen synthase kinase-3β, glycogen synthase, redox signaling, metabolic regulation, oxidative stress
- MeSH terms
- Animals, Antimycin A, Cells, Cultured, Cytosol, Endothelium, Vascular, Energy Metabolism, Enzyme Activation, Feedback, Glycogen Synthase, HeLa Cells, Humans, Hydrogen Peroxide, Kidney, Mitochondria, Neoplasm Proteins, Oxidation-Reduction, Umbilical Veins, 3T3 Cells, Oxidants, Reactive Oxygen Species, Calcium-Calmodulin-Dependent Protein Kinases, Muscle, Skeletal, Pyruvic Acid, Ribosomal Protein S6 Kinases, Mitogen-Activated Protein Kinases, MAP Kinase Signaling System, Glycogen Synthase Kinases, Glycogen Synthase Kinase 3, JNK Mitogen-Activated Protein Kinases, Mice
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