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Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels
Slick (Slo2.1) and Slack (Slo2.2) channels belong to the family of high-conductance K(+) channels and have been found widely distributed in the CNS. Both channels are activated by Na(+) and Cl(−) and, in addition, Slick channels are regulated by ATP. Therefore, the roles of these channels in regulat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210196/ https://www.ncbi.nlm.nih.gov/pubmed/25347289 http://dx.doi.org/10.1371/journal.pone.0110833 |
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author | Tejada, Maria A. Stople, Kathleen Hammami Bomholtz, Sofia Meinild, Anne-Kristine Poulsen, Asser Nyander Klaerke, Dan A. |
author_facet | Tejada, Maria A. Stople, Kathleen Hammami Bomholtz, Sofia Meinild, Anne-Kristine Poulsen, Asser Nyander Klaerke, Dan A. |
author_sort | Tejada, Maria A. |
collection | PubMed |
description | Slick (Slo2.1) and Slack (Slo2.2) channels belong to the family of high-conductance K(+) channels and have been found widely distributed in the CNS. Both channels are activated by Na(+) and Cl(−) and, in addition, Slick channels are regulated by ATP. Therefore, the roles of these channels in regulation of cell excitability as well as ion transport processes, like regulation of cell volume, have been hypothesized. It is the aim of this work to evaluate the sensitivity of Slick and Slack channels to small, fast changes in cell volume and to explore mechanisms, which may explain this type of regulation. For this purpose Slick and Slack channels were co-expressed with aquaporin 1 in Xenopus laevis oocytes and cell volume changes of around 5% were induced by exposure to hypotonic or hypertonic media. Whole-cell currents were measured by two electrode voltage clamp. Our results show that Slick channels are dramatically stimulated (196% of control) by cell swelling and inhibited (57% of control) by a decrease in cell volume. In contrast, Slack channels are totally insensitive to similar cell volume changes. The mechanism underlining the strong volume sensitivity of Slick channels needs to be further explored, however we were able to show that it does not depend on an intact actin cytoskeleton, ATP release or vesicle fusion. In conclusion, Slick channels, in contrast to the similar Slack channels, are the only high-conductance K(+) channels strongly sensitive to small changes in cell volume. |
format | Online Article Text |
id | pubmed-4210196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-42101962014-10-30 Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels Tejada, Maria A. Stople, Kathleen Hammami Bomholtz, Sofia Meinild, Anne-Kristine Poulsen, Asser Nyander Klaerke, Dan A. PLoS One Research Article Slick (Slo2.1) and Slack (Slo2.2) channels belong to the family of high-conductance K(+) channels and have been found widely distributed in the CNS. Both channels are activated by Na(+) and Cl(−) and, in addition, Slick channels are regulated by ATP. Therefore, the roles of these channels in regulation of cell excitability as well as ion transport processes, like regulation of cell volume, have been hypothesized. It is the aim of this work to evaluate the sensitivity of Slick and Slack channels to small, fast changes in cell volume and to explore mechanisms, which may explain this type of regulation. For this purpose Slick and Slack channels were co-expressed with aquaporin 1 in Xenopus laevis oocytes and cell volume changes of around 5% were induced by exposure to hypotonic or hypertonic media. Whole-cell currents were measured by two electrode voltage clamp. Our results show that Slick channels are dramatically stimulated (196% of control) by cell swelling and inhibited (57% of control) by a decrease in cell volume. In contrast, Slack channels are totally insensitive to similar cell volume changes. The mechanism underlining the strong volume sensitivity of Slick channels needs to be further explored, however we were able to show that it does not depend on an intact actin cytoskeleton, ATP release or vesicle fusion. In conclusion, Slick channels, in contrast to the similar Slack channels, are the only high-conductance K(+) channels strongly sensitive to small changes in cell volume. Public Library of Science 2014-10-27 /pmc/articles/PMC4210196/ /pubmed/25347289 http://dx.doi.org/10.1371/journal.pone.0110833 Text en © 2014 Tejada et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Tejada, Maria A. Stople, Kathleen Hammami Bomholtz, Sofia Meinild, Anne-Kristine Poulsen, Asser Nyander Klaerke, Dan A. Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title | Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title_full | Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title_fullStr | Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title_full_unstemmed | Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title_short | Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K(+) Channels |
title_sort | cell volume changes regulate slick (slo2.1), but not slack (slo2.2) k(+) channels |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4210196/ https://www.ncbi.nlm.nih.gov/pubmed/25347289 http://dx.doi.org/10.1371/journal.pone.0110833 |
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