A model system using confocal fluorescence microscopy for examining real-time intracellular sodium ion regulation

dc.contributor.authorLee, Jacqueline A.en
dc.contributor.authorCollings, David A.en
dc.contributor.authorGlover, Chris N.en
dc.date.accessioned2025-06-11T10:35:45Z
dc.date.available2025-06-11T10:35:45Z
dc.date.issued2016-08-15en
dc.description.abstractThe gills of euryhaline fish are the ultimate ionoregulatory tissue, achieving ion homeostasis despite rapid and significant changes in external salinity. Cellular handling of sodium is not only critical for salt and water balance but is also directly linked to other essential functions such as acid-base homeostasis and nitrogen excretion. However, although measurement of intracellular sodium ([Na+]i) is important for an understanding of gill transport function, it is challenging and subject to methodological artifacts. Using gill filaments from a model euryhaline fish, inanga (Galaxias maculatus), the suitability of the fluorescent dye CoroNa Green as a probe for measuring [Na+]i in intact ionocytes was confirmed via confocal microscopy. Cell viability was verified, optimal dye loading parameters were determined, and the dye-ion dissociation constant was measured. Application of the technique to freshwater- and 100% seawater-acclimated inanga showed salinity-dependent changes in branchial [Na+]i, whereas no significant differences in branchial [Na+]i were determined in 50% seawater-acclimated fish. This technique facilitates the examination of real-time changes in gill [Na+]i in response to environmental factors and may offer significant insight into key homeostatic functions associated with the fish gill and the principles of sodium ion transport in other tissues and organisms.en
dc.description.sponsorshipThe authors thank Manfred Ingerfeld for invaluable assistance with confocal microscopy and the many volunteers who helped with fish collection. This study was supported by a Royal Society of New Zealand Marsden Grant to C.N.G. ( UOC0711 ). C.N.G. is supported by a Campus Alberta Innovates Program Research Chair .en
dc.description.statusPeer-revieweden
dc.format.extent7en
dc.identifier.issn0003-2697en
dc.identifier.otherPubMed:27235170en
dc.identifier.otherORCID:/0000-0003-3863-5979/work/162946654en
dc.identifier.scopus84973889210en
dc.identifier.urihttp://www.scopus.com/inward/record.url?scp=84973889210&partnerID=8YFLogxKen
dc.identifier.urihttps://hdl.handle.net/1885/733758533
dc.language.isoenen
dc.rightsPublisher Copyright: © 2016 Elsevier Inc. All rights reserved.en
dc.sourceAnalytical Biochemistryen
dc.subjectAmphidromousen
dc.subjectFishen
dc.subjectGillen
dc.subjectIntracellular sodium concentrationen
dc.subjectLaser scanning confocal microscopyen
dc.subjectSalinity acclimationen
dc.titleA model system using confocal fluorescence microscopy for examining real-time intracellular sodium ion regulationen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage46en
local.bibliographicCitation.startpage40en
local.contributor.affiliationLee, Jacqueline A.; University of Canterburyen
local.contributor.affiliationCollings, David A.; School of Biological Sciencesen
local.contributor.affiliationGlover, Chris N.; University of Canterburyen
local.identifier.citationvolume507en
local.identifier.doi10.1016/j.ab.2016.05.008en
local.identifier.pure4ca814a7-ee3f-43a4-ab23-53b0036bcc10en
local.identifier.urlhttps://www.scopus.com/pages/publications/84973889210en
local.type.statusPublisheden

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