Elucidating Mitochondrial Electron Transport Chain Supercomplexes in the Heart During Ischemia–Reperfusion
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AIMS: Mitochondrial supercomplexes (SCs) are the large supramolecular assembly of individual electron transport chain (ETC) complexes that apparently provide highly efficient ATP synthesis and reduce electron leakage and reactive oxygen species (ROS) production. Oxidative stress during cardiac ischemia-reperfusion (IR) can result in degradation of SCs through oxidation of cardiolipin (CL). Also, IR induces calcium overload and enhances reactive oxygen species (mitROS) in mitochondria that result in the opening of the nonselective permeability transition pores (PTP). The opening of the PTP further compromises cellular energetics and increases mitROS ultimately leading to cell death. Here, we examined the role of PTP-induced mitROS in disintegration of SCs during cardiac IR. The relationship between mitochondrial PTP, ROS, and SCs was investigated using Langendorff-perfused rat hearts subjected to global ischemia (25 min) followed by short-time (5 min) or long-time (60 min) reperfusion in the presence or absence of the PTP inhibitor, sanglifehrin A (SfA), and the mitochondrial targeted ROS and electron scavenger, XJB-5-131. Also, the effects of CL deficiency on SC degradation, PTP, and mitROS were investigated in tafazzin knockdown (TazKD) mice. RESULTS: Cardiac IR induced PTP opening and mitROS generation, inhibited by SfA. Percent distributions of SCs were significantly affected by IR, and the effects were dependent on the reperfusion time and reversed by SfA and XJB-5-131. TazKD mice demonstrated a 40% lower SC I + III+IV with reduced basal mitochondrial PTP, ROS, and ETC complex activity. Innovation and Conclusion: Sustained reperfusion after cardiac ischemia induces disintegration of mitochondrial SCs, and PTP-induced ROS presumably play a causal role in SC disassembly. Antioxid. Redox Signal. 27, 57-69.
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Pharmacological inhibitors of CYPD including CsA, SfA, and JW47 limit MPT-driven necrosis and confer protection in multiple rodent models of disease in which oxidative stress and cytosolic Ca2+ overload constitute major etiological determinants (e.g., neuronal, cardiac, renal ischemia/reperfusion).
“Accordingly, pharmacological inhibitors of CYPD including cyclosporin A (CsA) [376 379–381], sanglifehrin A (SfA) [382, 383], and JW47 [384] limit MPT-driven necrosis and confer protection in multiple rodent models of disease in which oxidative stress and cytosolic Ca2+ overload constitute major etiological determinants (e.g., neuronal, cardiac, and renal ischemia/reperfusion).”
From Molecular mechanisms of cell death: recommendations of the nomenclature committee on cell death 2018. (2018) · cites this paper as [383]
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- Authors
- Jang, S., Lewis, T. S., Powers, C., Khuchua, Z., Baines, C. P., Wipf, P., & Javadov, S.
- Affiliations
- University of Puerto Rico, Medical Sciences Campus (PR)
- University of Pittsburgh (US)
- Cincinnati Children's Hospital Medical Center (US)
- University of Missouri (US)
- Corresponding author
- Javadov, Sabzali
- Venue
- Antioxidants & Redox Signaling
- Publisher
- SAGE Publications
- Published
- 2017-07
- Volume
- 27
- Issue
- 1
- Pages
- 57-69
- ISSN
- 1523-0864 (ISSN-L)
- 1557-7716
- PMC
- PMC5488255
- OpenAlex
- W2556127230
- Cited by
- 103
- References
- 69
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 14 · 2023: 7 · 2022: 11 · 2021: 10 · 2020: 9 · 2019: 10 · 2018: 11 · 2017: 15
- FWCI
- 6.23
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Antioxidants and Redox Signaling (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (R01HL094404, SC1HL118669, R01HL108867)
- National Center for Research Resources (G12RR003051)
- National Institute on Minority Health and Health Disparities (G12MD007600)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Pathology and Forensic Medicine › Cardiac Ischemia and Reperfusion
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- mitochondrial supercomplexes, electron transport chain, cardiac ischemia-reperfusion, mitochondrial permeability transition pore, mitochondrial reactive oxygen species, cardiolipin, tafazzin, sanglifehrin A, oxidative stress, calcium overload, mitochondrial dysfunction
- MeSH terms
- Mitochondrial Permeability Transition Pore, Animals, Cyclic N-Oxides, Disease Models, Animal, Electron Transport, Female, Lactones, Male, Mitochondria, Heart, Spiro Compounds, Myocardial Reperfusion Injury, Reactive Oxygen Species, Oxidative Stress, Mitochondrial Membrane Transport Proteins, Rats
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