13
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Cell Volume Changes Regulate Slick (Slo2.1), but Not Slack (Slo2.2) K + Channels

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          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.

          Related collections

          Most cited references31

          • Record: found
          • Abstract: found
          • Article: not found

          Physiology of cell volume regulation in vertebrates.

          The ability to control cell volume is pivotal for cell function. Cell volume perturbation elicits a wide array of signaling events, leading to protective (e.g., cytoskeletal rearrangement) and adaptive (e.g., altered expression of osmolyte transporters and heat shock proteins) measures and, in most cases, activation of volume regulatory osmolyte transport. After acute swelling, cell volume is regulated by the process of regulatory volume decrease (RVD), which involves the activation of KCl cotransport and of channels mediating K(+), Cl(-), and taurine efflux. Conversely, after acute shrinkage, cell volume is regulated by the process of regulatory volume increase (RVI), which is mediated primarily by Na(+)/H(+) exchange, Na(+)-K(+)-2Cl(-) cotransport, and Na(+) channels. Here, we review in detail the current knowledge regarding the molecular identity of these transport pathways and their regulation by, e.g., membrane deformation, ionic strength, Ca(2+), protein kinases and phosphatases, cytoskeletal elements, GTP binding proteins, lipid mediators, and reactive oxygen species, upon changes in cell volume. We also discuss the nature of the upstream elements in volume sensing in vertebrate organisms. Importantly, cell volume impacts on a wide array of physiological processes, including transepithelial transport; cell migration, proliferation, and death; and changes in cell volume function as specific signals regulating these processes. A discussion of this issue concludes the review.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Alterations in conserved Kir channel-PIP2 interactions underlie channelopathies.

            Inwardly rectifying K(+) (Kir) channels are important regulators of resting membrane potential and cell excitability. The activity of Kir channels is critically dependent on the integrity of channel interactions with phosphatidylinositol 4,5-bisphosphate (PIP(2)). Here we identify and characterize channel-PIP(2) interactions that are conserved among Kir family members. We find basic residues that interact with PIP(2), two of which have been associated with Andersen's and Bartter's syndromes. We show that several naturally occurring mutants decrease channel-PIP(2) interactions, leading to disease.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              The sodium-activated potassium channel is encoded by a member of the Slo gene family.

              Na(+)-activated potassium channels (K(Na)) have been identified in cardiomyocytes and neurons where they may provide protection against ischemia. We now report that K(Na) is encoded by the rSlo2 gene (also called Slack), the mammalian ortholog of slo-2 in C. elegans. rSlo2, heterologously expressed, shares many properties of native K(Na) including activation by intracellular Na(+), high conductance, and prominent subconductance states. In addition to activation by Na(+), we report that rSLO-2 channels are cooperatively activated by intracellular Cl(-), similar to C. elegans SLO-2 channels. Since intracellular Na(+) and Cl(-) both rise in oxygen-deprived cells, coactivation may more effectively trigger the activity of rSLO-2 channels in ischemia. In C. elegans, mutational and physiological analysis revealed that the SLO-2 current is a major component of the delayed rectifier. We demonstrate in C. elegans that slo-2 mutants are hypersensitive to hypoxia, suggesting a conserved role for the slo-2 gene subfamily.
                Bookmark

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                27 October 2014
                : 9
                : 10
                : e110833
                Affiliations
                [1 ]Department of Physiology and Biochemistry (IKVH), Faculty of Health and Medical Sciences, University of Copenhagen, Frederiksberg, Copenhagen, Denmark
                [2 ]Department of Biology, Faculty of Science, University of Copenhagen, Copenhagen, Denmark
                Dalhousie University, Canada
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MT KS AKM DK. Performed the experiments: MT KS SHB ANP. Analyzed the data: MT KS SHB. Contributed reagents/materials/analysis tools: AKM DK. Wrote the paper: MT AKM ANP DK.

                Article
                PONE-D-14-27018
                10.1371/journal.pone.0110833
                4210196
                25347289
                a39def08-94f1-45cb-90af-7bb08925fbf2
                Copyright @ 2014

                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 credited.

                History
                : 24 June 2014
                : 5 September 2014
                Page count
                Pages: 8
                Funding
                The work was supported by grants from the Danish Medical Research Council (Grant 0602-00021B), the Novonordisk Foundation, The Lundbeck Foundation (Lucens), The Fouger_Hartmann Foundation and Danish National Foundation for Advanced Technology. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Biochemistry
                Proteins
                Ion Channels
                Potassium Channels
                Calcium-Activated Potassium Channels
                Biophysics
                Cell Biology
                Cell Physiology
                Membrane Trafficking
                Cell Processes
                Actin Polymerization
                Protein Transport
                Osmotic Shock
                Custom metadata
                The authors confirm that all data underlying the findings are fully available without restriction. All data files are available from the Institutional Repository CURIS (Copenhagen University Research Information System). Specific URLs are located in the Supporting Information.

                Uncategorized
                Uncategorized

                Comments

                Comment on this article