Molecular identity of the mitochondrial permeability transition pore and its role in ischemia-reperfusion injury
- PMID: 25172387
- DOI: 10.1016/j.yjmcc.2014.08.015
Molecular identity of the mitochondrial permeability transition pore and its role in ischemia-reperfusion injury
Abstract
The mitochondrial permeability transition is a key event in cell death. Intense research efforts have been focused on elucidating the molecular components of the mitochondrial permeability transition pore (mPTP) to improve the understanding and treatment of various pathologies, including neurodegenerative disorders, cancer and cardiac diseases. Several molecular factors have been proposed as core components of the mPTP; however, further investigation has indicated that these factors are among a wide range of regulators. Thus, the scientific community lacks a clear model of the mPTP. Here, we review the molecular factors involved in the regulation and formation of the mPTP. Furthermore, we propose that the mitochondrial ATP synthase, specifically its c subunit, is the central core component of the mPTP complex. Moreover, we discuss the involvement of the mPTP in ischemia and reperfusion as well as the results of clinical studies targeting the mPTP to ameliorate ischemia-reperfusion injury. This article is part of a Special Issue entitled "Mitochondria: From Basic Mitochondrial Biology to Cardiovascular Disease".
Keywords: Apoptosis; Cell death; Ischemia reperfusion injury; Mitochondrial permeability transition pore, MPTP; Necrosis; Permeability transition pore, PTP.
Copyright © 2014 Elsevier Ltd. All rights reserved.
Similar articles
-
Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stress.Am J Physiol Heart Circ Physiol. 2007 Aug;293(2):H928-38. doi: 10.1152/ajpheart.01135.2006. Epub 2007 May 4. Am J Physiol Heart Circ Physiol. 2007. PMID: 17483234 Free PMC article.
-
The mitochondrial permeability transition pore and its role in myocardial ischemia reperfusion injury.J Mol Cell Cardiol. 2015 Jan;78:23-34. doi: 10.1016/j.yjmcc.2014.11.005. Epub 2014 Nov 14. J Mol Cell Cardiol. 2015. PMID: 25446182 Review.
-
The mitochondrial permeability transition pore: molecular nature and role as a target in cardioprotection.J Mol Cell Cardiol. 2015 Jan;78:100-6. doi: 10.1016/j.yjmcc.2014.09.023. Epub 2014 Sep 28. J Mol Cell Cardiol. 2015. PMID: 25268651 Free PMC article. Review.
-
Mitochondrial permeability transition pore-dependent necrosis.J Mol Cell Cardiol. 2023 Jan;174:47-55. doi: 10.1016/j.yjmcc.2022.11.003. Epub 2022 Nov 21. J Mol Cell Cardiol. 2023. PMID: 36410526 Free PMC article. Review.
-
Interplay between Ca2+ cycling and mitochondrial permeability transition pores promotes reperfusion-induced injury of cardiac myocytes.J Cell Mol Med. 2011 Nov;15(11):2478-85. doi: 10.1111/j.1582-4934.2010.01249.x. J Cell Mol Med. 2011. PMID: 21199327 Free PMC article.
Cited by
-
Comprehensive analysis of mitochondrial permeability transition pore activity in living cells using fluorescence-imaging-based techniques.Nat Protoc. 2016 Jun;11(6):1067-80. doi: 10.1038/nprot.2016.064. Epub 2016 May 12. Nat Protoc. 2016. PMID: 27172167
-
Chronology of mitochondrial and cellular events during skeletal muscle ischemia-reperfusion.Am J Physiol Cell Physiol. 2016 Jun 1;310(11):C968-82. doi: 10.1152/ajpcell.00356.2015. Epub 2016 Apr 13. Am J Physiol Cell Physiol. 2016. PMID: 27076618 Free PMC article. Review.
-
Meldonium, as a potential neuroprotective agent, promotes neuronal survival by protecting mitochondria in cerebral ischemia-reperfusion injury.J Transl Med. 2024 Aug 15;22(1):771. doi: 10.1186/s12967-024-05222-7. J Transl Med. 2024. PMID: 39148053 Free PMC article.
-
The expression of oxidative stress genes related to myocardial ischemia reperfusion injury in patients with ST-elevation myocardial infarction.World J Emerg Med. 2022;13(2):106-113. doi: 10.5847/wjem.j.1920-8642.2022.021. World J Emerg Med. 2022. PMID: 35237363 Free PMC article.
-
Comprehensive Analysis of Mitochondrial Dynamics Alterations in Heart Diseases.Int J Mol Sci. 2023 Feb 8;24(4):3414. doi: 10.3390/ijms24043414. Int J Mol Sci. 2023. PMID: 36834825 Free PMC article. Review.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources