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...

Descripción completa

Detalles Bibliográficos
Autores principales: Endlicher, René, Drahota, Zdeněk, Štefková, Kateřina, Červinková, Zuzana, Kučera, Otto
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