Cargando…
The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State
The mitochondrial permeability transition pore (MPTP) is a calcium-dependent, ion non-selective membrane pore with a wide range of functions. Although the MPTP has been studied for more than 50 years, its molecular structure remains unclear. Short-term (reversible) opening of the MPTP protects cells...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177258/ https://www.ncbi.nlm.nih.gov/pubmed/37174672 http://dx.doi.org/10.3390/cells12091273 |
_version_ | 1785040596088389632 |
---|---|
author | Endlicher, René Drahota, Zdeněk Štefková, Kateřina Červinková, Zuzana Kučera, Otto |
author_facet | Endlicher, René Drahota, Zdeněk Štefková, Kateřina Červinková, Zuzana Kučera, Otto |
author_sort | Endlicher, René |
collection | PubMed |
description | The mitochondrial permeability transition pore (MPTP) is a calcium-dependent, ion non-selective membrane pore with a wide range of functions. Although the MPTP has been studied for more than 50 years, its molecular structure remains unclear. Short-term (reversible) opening of the MPTP protects cells from oxidative damage and enables the efflux of Ca(2+) ions from the mitochondrial matrix and cell signaling. However, long-term (irreversible) opening induces processes leading to cell death. Ca(2+) ions, reactive oxygen species, and changes in mitochondrial membrane potential regulate pore opening. The sensitivity of the pore to Ca(2+) ions changes as an organism ages, and MPTP opening plays a key role in the pathogenesis of many diseases. Most studies of the MPTP have focused on elucidating its molecular structure. However, understanding the mechanisms that will inhibit the MPTP may improve the treatment of diseases associated with its opening. To evaluate the functional state of the MPTP and its inhibitors, it is therefore necessary to use appropriate methods that provide reproducible results across laboratories. This review summarizes our current knowledge of the function and regulation of the MPTP. The latter part of the review introduces two optimized methods for evaluating the functional state of the pore under standardized conditions. |
format | Online Article Text |
id | pubmed-10177258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101772582023-05-13 The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State Endlicher, René Drahota, Zdeněk Štefková, Kateřina Červinková, Zuzana Kučera, Otto Cells Review The mitochondrial permeability transition pore (MPTP) is a calcium-dependent, ion non-selective membrane pore with a wide range of functions. Although the MPTP has been studied for more than 50 years, its molecular structure remains unclear. Short-term (reversible) opening of the MPTP protects cells from oxidative damage and enables the efflux of Ca(2+) ions from the mitochondrial matrix and cell signaling. However, long-term (irreversible) opening induces processes leading to cell death. Ca(2+) ions, reactive oxygen species, and changes in mitochondrial membrane potential regulate pore opening. The sensitivity of the pore to Ca(2+) ions changes as an organism ages, and MPTP opening plays a key role in the pathogenesis of many diseases. Most studies of the MPTP have focused on elucidating its molecular structure. However, understanding the mechanisms that will inhibit the MPTP may improve the treatment of diseases associated with its opening. To evaluate the functional state of the MPTP and its inhibitors, it is therefore necessary to use appropriate methods that provide reproducible results across laboratories. This review summarizes our current knowledge of the function and regulation of the MPTP. The latter part of the review introduces two optimized methods for evaluating the functional state of the pore under standardized conditions. MDPI 2023-04-27 /pmc/articles/PMC10177258/ /pubmed/37174672 http://dx.doi.org/10.3390/cells12091273 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Endlicher, René Drahota, Zdeněk Štefková, Kateřina Červinková, Zuzana Kučera, Otto The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title | The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title_full | The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title_fullStr | The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title_full_unstemmed | The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title_short | The Mitochondrial Permeability Transition Pore—Current Knowledge of Its Structure, Function, and Regulation, and Optimized Methods for Evaluating Its Functional State |
title_sort | mitochondrial permeability transition pore—current knowledge of its structure, function, and regulation, and optimized methods for evaluating its functional state |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10177258/ https://www.ncbi.nlm.nih.gov/pubmed/37174672 http://dx.doi.org/10.3390/cells12091273 |
work_keys_str_mv | AT endlicherrene themitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT drahotazdenek themitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT stefkovakaterina themitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT cervinkovazuzana themitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT kuceraotto themitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT endlicherrene mitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT drahotazdenek mitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT stefkovakaterina mitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT cervinkovazuzana mitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate AT kuceraotto mitochondrialpermeabilitytransitionporecurrentknowledgeofitsstructurefunctionandregulationandoptimizedmethodsforevaluatingitsfunctionalstate |