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

• Published in: Analytical biochemistry Vol. 507; pp. 40 - 46
• Main Authors: Lee, Jacqueline A., Collings, David A., Glover, Chris N.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.08.2016
• Subjects: Amphidromous; Animals; Cell Survival; cell viability; confocal microscopy; dissociation; environmental factors; euryhaline species; excretion; Fish; fluorescence microscopy; fluorescent dyes; Galaxias maculatus; Gill; gills; Gills - cytology; Gills - metabolism; homeostasis; Intracellular sodium concentration; Ion Transport; Ions - metabolism; Laser scanning confocal microscopy; Microscopy, Confocal; Microscopy, Fluorescence; Models, Biological; nitrogen; Osmeriformes - metabolism; saline water; salinity; Salinity acclimation; sodium; Sodium - metabolism; Time Factors; Gill; SW; NKA; DMSO; Intracellular sodium concentration; [Na+]i; NHE; Amphidromous; FW; ANOVA; Fish; Laser scanning confocal microscopy; Salinity acclimation
• ISSN: 0003-2697; 1096-0309; 1096-0309
• DOI: 10.1016/j.ab.2016.05.008

The 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.