Cargando…
Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria
Previous studies have demonstrated several molecularly distinct players involved in mitochondrial Ca(2+) uptake. In the present study, electrophysiological recordings on mitoplasts that were isolated from HeLa cells were performed in order to biophysically and pharmacologically characterize Ca(2+) c...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3696464/ https://www.ncbi.nlm.nih.gov/pubmed/23397170 http://dx.doi.org/10.1007/s00424-013-1224-1 |
_version_ | 1782275124413595648 |
---|---|
author | Bondarenko, Alexander I. Jean-Quartier, Claire Malli, Roland Graier, Wolfgang F. |
author_facet | Bondarenko, Alexander I. Jean-Quartier, Claire Malli, Roland Graier, Wolfgang F. |
author_sort | Bondarenko, Alexander I. |
collection | PubMed |
description | Previous studies have demonstrated several molecularly distinct players involved in mitochondrial Ca(2+) uptake. In the present study, electrophysiological recordings on mitoplasts that were isolated from HeLa cells were performed in order to biophysically and pharmacologically characterize Ca(2+) currents across the inner mitochondrial membrane. In mitoplast-attached configuration with 105 mM Ca(2+) as a charge carrier, three distinct channel conductances of 11, 23, and 80 pS were observed. All types of mitochondrial currents were voltage-dependent and essentially depended on the presence of Ca(2+) in the pipette. The 23 pS channel exhibited burst kinetics. Though all channels were sensitive to ruthenium red, their sensitivity was different. The 11 and 23 pS channels exhibited a lower sensitivity to ruthenium red than the 80 pS channel. The activities of all channels persisted in the presence of cylosporin A, CGP 37187, various K(+)-channel inhibitors, and Cl(−) channel blockers disodium 4,4′-diisothiocyanatostilbene-2,2′-disulfonate and niflumic acid. Collectively, our data identified multiple conductances of Ca(2+) currents in mitoplasts isolated from HeLa cells, thus challenging the dogma of only one unique mitochondrial Ca(2+) uniporter. |
format | Online Article Text |
id | pubmed-3696464 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-36964642013-07-02 Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria Bondarenko, Alexander I. Jean-Quartier, Claire Malli, Roland Graier, Wolfgang F. Pflugers Arch Ion Channels, Receptors and Transporters Previous studies have demonstrated several molecularly distinct players involved in mitochondrial Ca(2+) uptake. In the present study, electrophysiological recordings on mitoplasts that were isolated from HeLa cells were performed in order to biophysically and pharmacologically characterize Ca(2+) currents across the inner mitochondrial membrane. In mitoplast-attached configuration with 105 mM Ca(2+) as a charge carrier, three distinct channel conductances of 11, 23, and 80 pS were observed. All types of mitochondrial currents were voltage-dependent and essentially depended on the presence of Ca(2+) in the pipette. The 23 pS channel exhibited burst kinetics. Though all channels were sensitive to ruthenium red, their sensitivity was different. The 11 and 23 pS channels exhibited a lower sensitivity to ruthenium red than the 80 pS channel. The activities of all channels persisted in the presence of cylosporin A, CGP 37187, various K(+)-channel inhibitors, and Cl(−) channel blockers disodium 4,4′-diisothiocyanatostilbene-2,2′-disulfonate and niflumic acid. Collectively, our data identified multiple conductances of Ca(2+) currents in mitoplasts isolated from HeLa cells, thus challenging the dogma of only one unique mitochondrial Ca(2+) uniporter. Springer Berlin Heidelberg 2013-02-09 2013 /pmc/articles/PMC3696464/ /pubmed/23397170 http://dx.doi.org/10.1007/s00424-013-1224-1 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/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 Malli, Roland Graier, Wolfgang F. Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title | Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title_full | Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title_fullStr | Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title_full_unstemmed | Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title_short | Characterization of distinct single-channel properties of Ca(2+) inward currents in mitochondria |
title_sort | characterization of distinct single-channel properties of ca(2+) inward currents in mitochondria |
topic | Ion Channels, Receptors and Transporters |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3696464/ https://www.ncbi.nlm.nih.gov/pubmed/23397170 http://dx.doi.org/10.1007/s00424-013-1224-1 |
work_keys_str_mv | AT bondarenkoalexanderi characterizationofdistinctsinglechannelpropertiesofca2inwardcurrentsinmitochondria AT jeanquartierclaire characterizationofdistinctsinglechannelpropertiesofca2inwardcurrentsinmitochondria AT malliroland characterizationofdistinctsinglechannelpropertiesofca2inwardcurrentsinmitochondria AT graierwolfgangf characterizationofdistinctsinglechannelpropertiesofca2inwardcurrentsinmitochondria |