The DOI matches its Crossref record; 60 of the 61 references it cites were found in a registry or an index.
A Mitochondrial Oscillator Dependent on Reactive Oxygen Species
Open accessAbstract
We describe a unique mitochondrial oscillator that depends on oxidative phosphorylation, reactive oxygen species (ROS), and mitochondrial inner membrane ion channels. Cell-wide synchronized oscillations in mitochondrial membrane potential (Delta Psi(m)), NADH, and ROS production have been recently described in isolated cardiomyocytes, and we have hypothesized that the balance between superoxide anion efflux through inner membrane anion channels and the intracellular ROS scavenging capacity play a key role in the oscillatory mechanism. Here, we formally test the hypothesis using a computational model of mitochondrial energetics and Ca(2+) handling including mitochondrial ROS production, cytoplasmic ROS scavenging, and ROS activation of inner membrane anion flux. The mathematical model reproduces the period and phase of the observed oscillations in Delta Psi(m), NADH, and ROS. Moreover, we experimentally verify model predictions that the period of the oscillator can be modulated by altering the concentration of ROS scavengers or the rate of oxidative phosphorylation, and that the redox state of the glutathione pool oscillates. In addition to its role in cellular dysfunction during metabolic stress, the period of the oscillator can be shown to span a wide range, from milliseconds to hours, suggesting that it may also be a mechanism for physiological timekeeping and/or redox signaling.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In endothelial cells, blocking the effect of NO• to compete for O2 at complex IV with an NOS inhibitor enhanced the rate of O2 consumption (respiration) at very low O2 concentrations (89).”
From Mitochondrial reactive oxygen species production in excitable cells: Modulators of mitochondrial and cell function (2009) · cites this paper as [89]
Citations
Cites
Aebi, H. (1984) · Methods in Enzymology · doi:10.1016/s0076-6879(84)05016-3 · Cited by 25,696
Free Radicals in the Physiological Control of Cell Function
Dröge, W. (2002) · Physiological Reviews · doi:10.1152/physrev.00018.2001 · Cited by 9,855
Self-organized criticality: An explanation of the 1/ f noise
Bak, P., Tang, C., & Wiesenfeld, K. A. (1987) · Physical Review Letters · doi:10.1103/physrevlett.59.381 · Cited by 7,644
Hydroperoxide metabolism in mammalian organs.
Chance, B., Sies, H., & Boveris, A. (1979) · Physiological Reviews · doi:10.1152/physrev.1979.59.3.527 · Cited by 5,827
Mitochondrial formation of reactive oxygen species
Turrens, J. F. (2003) · The Journal of Physiology · doi:10.1113/jphysiol.2003.049478 · Cited by 5,084
Oxyl radicals, redox-sensitive signalling cascades and antioxidants
Genestra, M. (2007) · Cellular Signalling · doi:10.1016/j.cellsig.2007.04.009 · Cited by 4,930
Carlberg, I., & Mannervik, B. (1985) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(85)13062-4 · Cited by 3,055
Wendel, A. (1981) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(81)77046-0 · Cited by 3,032
Nìcolis, G., & Prigogine, I. (1977) · CERN Document Server (European Organization for Nuclear Research) · Cited by 2,064
Generation of superoxide anion by the NADH dehydrogenase of bovine heart mitochondria
Turrens, J. F., & Boveris, A. (1980) · Biochemical Journal · doi:10.1042/bj1910421 · Cited by 1,601
Topology of superoxide production from different sites in the mitochondrial electron transport chain
St-Pierre, J., Buckingham, J. A., Roebuck, S. J., & Brand, M. D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207217200 · Cited by 1,545
Reactive Oxygen Species (Ros-Induced) Ros Release
Zorov, D. B., Filburn, C. R., Klotz, L.-O., Zweier, J. L., & Sollott, S. J. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.7.1001 · Cited by 1,412
Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria
Turrens, J. F., Alexandre, A., & Lehninger, A. L. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90293-0 · Cited by 1,214
Critical Phenomena in Natural Sciences
Sornette, D. (2000) · Springer series in synergetics · doi:10.1007/978-3-662-04174-1 · Cited by 1,213
GODDARD, L. S. (1963) · Nature · doi:10.1038/197525a0 · Cited by 1,092
Subcellular Distribution of Superoxide Dismutases (SOD) in Rat Liver
Okado‐Matsumoto, A., & Fridovich, I. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105395200 · Cited by 1,036
Schnakenberg, J. (1978) · Berichte der Bunsengesellschaft für physikalische Chemie · doi:10.1002/bbpc.197800155 · Cited by 818
Repetitive transient rises in cytoplasmic free calcium in hormone-stimulated hepatocytes
Woods, N. M., Cuthbertson, K., & Cobbold, P. H. (1986) · Nature · doi:10.1038/319600a0 · Cited by 793
Molecular and Cellular Aspects of Thiol–Disulfide Exchange
Gilbert, H. (1990) · Advances in enzymology and related areas of molecular biology/Advances in enzymology and related subjects · doi:10.1002/9780470123096.ch2 · Cited by 770
Sturtz, L. A., Diekert, K., Jensen, L. T., Lill, R., & Culotta, V. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105296200 · Cited by 735
Han, D., Antunes, F., Canali, R., Rettori, D., & Cadenas, E. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m210269200 · Cited by 711
McEnery, M. W., Snowman, A. M., Trifiletti, R. R., & Snyder, S. H. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.8.3170 · Cited by 708
Kushnareva, Y., Murphy, A. N., & Andreyev, A. Y. (2002) · Biochemical Journal · doi:10.1042/bj20021121 · Cited by 696
Berridge, M. J., & Galione, A. (1988) · The FASEB Journal · doi:10.1096/fasebj.2.15.2847949 · Cited by 686
Sornette, D. (2014) · doi:10.1007/3-540-33182-4 · Cited by 627
Biochemical Oscillations and Cellular Rhythms
Goldbeter, A., & Berridge, M. J. (1996) · Cambridge University Press eBooks · doi:10.1017/cbo9780511608193 · Cited by 611
Aon, M. A., Cortassa, S., Marbán, E., & O'Rourke, B. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m302673200 · Cited by 521
Self-citationRegulation of brain mitochondrial H 2 O 2 production by membrane potential and NAD(P)H redox state
Starkov, A. A., & Fiskum, G. M. (2003) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2003.01908.x · Cited by 503
Antioxidant and prooxidant mechanisms in the regulation of redox(y)-sensitive transcription factors
Haddad, J. J. (2002) · Cellular Signalling · doi:10.1016/s0898-6568(02)00053-0 · Cited by 430
Reduction and inactivation of superoxide dismutase by hydrogen peroxide
Bray, R. C., Cockle, S. A., Fielden, E. M., Roberts, P. B., Rotilio, G., & Calabrese, L. (1974) · Biochemical Journal · doi:10.1042/bj1390043 · Cited by 394
An Integrated Model of Cardiac Mitochondrial Energy Metabolism and Calcium Dynamics
Cortassa, S. C., Aon, M. A., Marbán, E., Winslow, R. L., & O'Rourke, B. P. (2003) · Biophysical Journal · doi:10.1016/s0006-3495(03)75079-6 · Cited by 389
Self-citationRooney, T. A., Sass, E. J., & Thomas, A. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)71469-5 · Cited by 371
Martin, K. R., & Barrett, J. C. (2002) · Human & Experimental Toxicology · doi:10.1191/0960327102ht213oa · Cited by 363
Superoxide anion permeability of phospholipid membranes and chloroplast thylakoids
Takahashi, M., & Asada, K. (1983) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(83)90325-9 · Cited by 309
Oscillations of Membrane Current and Excitability Driven by Metabolic Oscillations in Heart Cells
O'Rourke, B. P., Ramza, B. M., & Marbán, E. (1994) · Science · doi:10.1126/science.8052856 · Cited by 281
Self-citationPatch-clamping of the inner mitochondrial membrane reveals a voltage-dependent ion channel
Sorgato, M. C., Keller, B. U., & Stühmer, W. (1987) · Nature · doi:10.1038/330498a0 · Cited by 245
Lesnefsky, E. J., Tandler, B., Ye, J., Slabe, T. J., Turkaly, J. S., & Hoppel, C. L. (1997) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1997.273.3.h1544 · Cited by 229
Percolation and criticality in a mitochondrial network
Aon, M. A., Cortassa, S. C., & O'Rourke, B. P. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0307156101 · Cited by 225
Self-citationLongo, E., Tornheim, K., Deeney, J. T., Varnum, B. A., Tillotson, D. L., Prentki, M., & Corkey, B. E. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)31587-4 · Cited by 215
Subcellular metabolic transients and mitochondrial redox waves in heart cells
Romashko, D. N., Marbán, E., & O'Rourke, B. P. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.4.1618 · Cited by 211
Self-citationKinnally, K. W., Zorov, D. B., Antonenko, Y. N., Snyder, S. H., McEnery, M. W., & Tedeschi, H. (1993) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.90.4.1374 · Cited by 205
Antioxidants in myocardial ischemia–reperfusion injury: therapeutic potential and basic mechanisms
Marczin, N., El-Habashi, N., Hoare, G. S., Bundy, R. E., & Yacoub, M. H. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2003.08.037 · Cited by 165
Pathophysiological and protective roles of mitochondrial ion channels
O'Rourke, B. P. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00023.x · Cited by 148
Self-citationThiol labeling with bromobimanes
Kosower, N. S., & Kosower, E. M. (1987) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(87)43015-2 · Cited by 147
Properties of the inner membrane anion channel in intact mitochondria
Beavis, A. D. (1992) · Journal of Bioenergetics and Biomembranes · doi:10.1007/bf00769534 · Cited by 142
Mechanisms of Ischemic Preconditioning in Rat Myocardium
Vuorinen, K. H., Ylitalo, K. V., PEUHKURINEN, K. J., Raatikainen, P. M. J., Ala-Rämi, A., & Hassinen, I. E. (1995) · Circulation · doi:10.1161/01.cir.91.11.2810 · Cited by 130
McAdam, M. E., Fox, R. A., Lavelle, F., & Fielden, E. M. (1977) · Biochemical Journal · doi:10.1042/bj1650071 · Cited by 123
Hardy, L., Clark, J. B., Darley-Usmar, V. M., Smith, D. R., & Stone, D. (1991) · Biochemical Journal · doi:10.1042/bj2740133 · Cited by 123
A model of O·2 -generation in the complex III of the electron transport chain
Demin, O. V., Kholodenko, B. Ν., & Skulachev, V. P. (1998) · Springer eBooks · doi:10.1007/978-1-4615-5653-4_3 · Cited by 98
A model of O·2 - generation in the complex III of the electron transport chain
Demin, O. V., Kholodenko, B. Ν., & Скулачев, В. П. (1998) · Molecular and Cellular Biochemistry · doi:10.1023/a:1006849920918 · Cited by 94
Copper, Zinc Superoxide Dismutase and H2O2
Liochev, S. I., & Fridovich, I. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m204726200 · Cited by 88
Brown, H. F., Kimura, J., Noble, D., Noble, S. J., & Taupignon, A. (1984) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.1984.0067 · Cited by 82
Sustained oscillations of ionic constituents of mitochondria
Chance, B., & Yoshioka, T. (1966) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(66)90435-8 · Cited by 71
108-pS Channel in Brown Fat Mitochondria Might Be Identical to the Inner Membrane Anion Channel
Borecký, J., Ježek, P., & Siemen, D. (1997) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)38955-5 · Cited by 66
Dynamic Biological Organization
Aon, M. A., & Cortassa, S. C. (1997) · Springer eBooks · doi:10.1007/978-94-011-5828-2 · Cited by 63
Self-citationOscillatory systems in mitochondria
Gooch, V. D., & Packer, L. (1974) · Biochimica et Biophysica Acta (BBA) - Reviews on Bioenergetics · doi:10.1016/0304-4173(74)90002-0 · Cited by 54
Cardiac ischemia/reperfusion, aging, and redox-dependent alterations in mitochondrial function
Sadek, H. A., Nulton-Persson, A. C., Szweda, P. A., & Szweda, L. I. (2003) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2003.09.029 · Cited by 52
Dynamic Biological Organization : Fundamentals as Applied to Cellular Systems
Aon, M. A., & Cortassa, S. C. (2012) · Cited by 50
Self-citationCircadian and Ultradian Clock-controlled Rhythms in Unicellular Microorganisms
Lloyd, D. (1997) · Advances in microbial physiology/Advances in Microbial Physiology · doi:10.1016/s0065-2911(08)60019-3 · Cited by 42
Evtodienko, Y. V. (2000) · PubMed · Cited by 6
Research works printed but not linked: 1
- Chance, 1965, Properties and kinetics of reduced pyridine nucleotide fluorescence of the isolated and in vivo rat heart, Biochem. Z., 341, 357
Cited by
Sorted by citations
Mitochondrial ROS-induced ROS release: An update and review
Zorov, D. B., Juhaszova, M., & Sollott, S. J. (2006) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2006.04.029 · Cited by 1,099
Mitochondria in homeostasis of reactive oxygen species in cell, tissues, and organism
Ježek, P., & Plecitá‐Hlavatá, L. (2005) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2005.05.013 · Cited by 753
Mitochondrial Signaling in Mammalian Cells Activated by Red and Near‐IR Radiation
Karu, T. I. (2008) · Photochemistry and Photobiology · doi:10.1111/j.1751-1097.2008.00394.x · Cited by 575
Monogenic Mitochondrial Disorders
Koopman, W. J. H., Willems, P. H. G. M., & Smeitink, J. A. M. (2012) · New England Journal of Medicine · doi:10.1056/nejmra1012478 · Cited by 527
Stowe, D. F., & Camara, A. K. S. (2009) · Antioxidants & Redox Signaling · doi:10.1089/ars.2008.2331 · Cited by 471
Metadata
- Authors
- Cortassa, S., Aon, M. A., Winslow, R. L., & O’Rourke, B.
- Affiliations
- Johns Hopkins University (US)
- Venue
- Biophysical Journal
- Publisher
- Elsevier BV
- Published
- 2004-09
- Volume
- 87
- Issue
- 3
- Pages
- 2060-2073
- ISSN
- 0006-3495 (ISSN-L)
- PMC
- PMC1304608
- OpenAlex
- W2058028795
- Cited by
- 235
- References
- 61
- Citations by year
- 2026: 9 · 2025: 7 · 2024: 10 · 2023: 11 · 2022: 13 · 2021: 5 · 2020: 5 · 2019: 4 · 2018: 12 · 2017: 11 · 2016: 12 · 2015: 9 · 2014: 12 · 2013: 17 · 2012: 16
- FWCI
- 3.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biophysical Journal (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (P50-HL52307, R01-HL-60133-01, R01HL105239, R01HL054598, R01HL060133, P50HL052307, R01HL54598)
- 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
- Physical Sciences › Physics and Astronomy › Statistical and Nonlinear Physics › Nonlinear Dynamics and Pattern Formation
- Keywords
- reactive oxygen species, oxidative phosphorylation, cardiomyocytes, mitochondrial ROS production, glutathione redox state, calcium handling, redox signaling
- MeSH terms
- Animals, Calcium, Cytosol, Glutathione, Glutathione Peroxidase, Glutathione Reductase, Guinea Pigs, Hydrogen Peroxide, Image Processing, Computer-Assisted, Kinetics, Lasers, Membrane Potentials, Microscopy, Fluorescence, Mitochondria, Models, Biological, Models, Theoretical, Oligomycins, Oscillometry, Oxygen, Superoxide Dismutase, Reperfusion Injury, Reactive Oxygen Species, Photons, Myocytes, Cardiac
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review