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Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane

A protein referred to as CCDC109A and then renamed to mitochondrial calcium uniporter (MCU) has recently been shown to accomplish mitochondrial Ca(2+) uptake in different cell types. In this study, we investigated whole-mitoplast inward cation currents and single Ca(2+) channel activities in mitopla...

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Autores principales: Bondarenko, Alexander I., Jean-Quartier, Claire, Parichatikanond, Warisara, Alam, Muhammad Rizwan, Waldeck-Weiermair, Markus, Malli, Roland, Graier, Wolfgang F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020763/
https://www.ncbi.nlm.nih.gov/pubmed/24162235
http://dx.doi.org/10.1007/s00424-013-1383-0
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author Bondarenko, Alexander I.
Jean-Quartier, Claire
Parichatikanond, Warisara
Alam, Muhammad Rizwan
Waldeck-Weiermair, Markus
Malli, Roland
Graier, Wolfgang F.
author_facet Bondarenko, Alexander I.
Jean-Quartier, Claire
Parichatikanond, Warisara
Alam, Muhammad Rizwan
Waldeck-Weiermair, Markus
Malli, Roland
Graier, Wolfgang F.
author_sort Bondarenko, Alexander I.
collection PubMed
description A protein referred to as CCDC109A and then renamed to mitochondrial calcium uniporter (MCU) has recently been shown to accomplish mitochondrial Ca(2+) uptake in different cell types. In this study, we investigated whole-mitoplast inward cation currents and single Ca(2+) channel activities in mitoplasts prepared from stable MCU knockdown HeLa cells using the patch-clamp technique. In whole-mitoplast configuration, diminution of MCU considerably reduced inward Ca(2+) and Na(+) currents. This was accompanied by a decrease in occurrence of single channel activity of the intermediate conductance mitochondrial Ca(2+) current (i-MCC). However, ablation of MCU yielded a compensatory 2.3-fold elevation in the occurrence of the extra large conductance mitochondrial Ca(2+) current (xl-MCC), while the occurrence of bursting currents (b-MCC) remained unaltered. These data reveal i-MCC as MCU-dependent current while xl-MCC and b-MCC seem to be rather MCU-independent, thus, pointing to the engagement of at least two molecularly distinct mitochondrial Ca(2+) channels.
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spelling pubmed-40207632014-06-25 Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane Bondarenko, Alexander I. Jean-Quartier, Claire Parichatikanond, Warisara Alam, Muhammad Rizwan Waldeck-Weiermair, Markus Malli, Roland Graier, Wolfgang F. Pflugers Arch Ion Channels, Receptors and Transporters A protein referred to as CCDC109A and then renamed to mitochondrial calcium uniporter (MCU) has recently been shown to accomplish mitochondrial Ca(2+) uptake in different cell types. In this study, we investigated whole-mitoplast inward cation currents and single Ca(2+) channel activities in mitoplasts prepared from stable MCU knockdown HeLa cells using the patch-clamp technique. In whole-mitoplast configuration, diminution of MCU considerably reduced inward Ca(2+) and Na(+) currents. This was accompanied by a decrease in occurrence of single channel activity of the intermediate conductance mitochondrial Ca(2+) current (i-MCC). However, ablation of MCU yielded a compensatory 2.3-fold elevation in the occurrence of the extra large conductance mitochondrial Ca(2+) current (xl-MCC), while the occurrence of bursting currents (b-MCC) remained unaltered. These data reveal i-MCC as MCU-dependent current while xl-MCC and b-MCC seem to be rather MCU-independent, thus, pointing to the engagement of at least two molecularly distinct mitochondrial Ca(2+) channels. Springer Berlin Heidelberg 2013-10-27 2014 /pmc/articles/PMC4020763/ /pubmed/24162235 http://dx.doi.org/10.1007/s00424-013-1383-0 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Ion Channels, Receptors and Transporters
Bondarenko, Alexander I.
Jean-Quartier, Claire
Parichatikanond, Warisara
Alam, Muhammad Rizwan
Waldeck-Weiermair, Markus
Malli, Roland
Graier, Wolfgang F.
Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title_full Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title_fullStr Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title_full_unstemmed Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title_short Mitochondrial Ca(2+) uniporter (MCU)-dependent and MCU-independent Ca(2+) channels coexist in the inner mitochondrial membrane
title_sort mitochondrial ca(2+) uniporter (mcu)-dependent and mcu-independent ca(2+) channels coexist in the inner mitochondrial membrane
topic Ion Channels, Receptors and Transporters
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4020763/
https://www.ncbi.nlm.nih.gov/pubmed/24162235
http://dx.doi.org/10.1007/s00424-013-1383-0
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