Quantitative localization of Na-K pump sites in the frog sacculus
- 31 July 1984
- journal article
- research article
- Published by Springer Nature in Journal of Neurocytology
- Vol. 13 (4), 617-638
- https://doi.org/10.1007/bf01148082
Abstract
The Na-K pump site distribution within the macula, perimacula, and wall epithelia of the sacculus in the frog inner ear was examined with quantitative [3H]ouabain autoradiography. Excised tissue was incubated for 10–30 min (23 ° C) in micromolar concentrations of high specific activity [3H]ouabain (14–70 βCi mT−1, 5–15 Ci mmor−1), washed for 30 min (4 ° C), then rapidly frozen (−175 ° C) and processed for light and electron microscope autoradiography. Control experiments based on (1) high K+ (50 mm) in the incubation and (2) low specific activity [3H]Jouabain (1 mM, 0.013–0.025 Ci mmol−1) indicated negligible nonspecific binding of the [3H]ouabain. Measurable levels of specific [3H]ouabain binding occurred in all saccular regions examined. Binding was localized to the basolateral cell membranes with no detectable binding to the apical membranes. [3H]ouabain binding across the apical-basal axis of the saccule macular epithelium was nonuniform. Binding was low in the apical region, rose to a peak in the middle two-thirds, and then fell again close to the basement membrane. Electron microscope autoradiography suggested that this peak was due to ouabain binding to nerve terminals. Denervation of the sacculus eliminated the peak in [3H]ouabain binding and quantitative grain density analysis revealed that 45% of the Na-K pumps within the saccule macula were located on the nerve terminals. Na-K pump site density per unit volume was estimated by quantitative grain density analysis and the following values were obtained (sites μm−3 × 103, means ± S.E.M.): saccule macula, 1.9 ± 0.2; saccule perimacula, 1.1 ± 0.1; saccule wall, 2.3 ± 0.3. Stereological analysis of conventionally fixed tissue was used to estimate overall plasma membrane surface area per unit volume (S v). Na-K pump site densities per unit membrane area for the various regions were calculated by combining the autoradiographical and Stereological data. The following values were obtained (sites μm−2 ± 25%): saccule macula, 2500; saccule perimacula, 2500. Values for individual cells within the macula (sites μm−2 ± 25%) were: hair cells, 3000; nerve terminals, 3000; supporting cells, 1500.This publication has 37 references indexed in Scilit:
- Distribution of transport proteins over animal cell membranesThe Journal of Membrane Biology, 1984
- Ultrastructure of Na,K-transport vesicles reconstituted with purified renal Na,K-ATPase.The Journal of cell biology, 1980
- [3H]ouabain autoradiography of frog retina.The Journal of cell biology, 1980
- Immunocytochemical localization of the sodium, potassium activated ATPase in knifefish brainJournal of Neurocytology, 1977
- Localization of Na+-pump sites in frog skin.The Journal of cell biology, 1977
- Histochemical localization of potassium-stimulated P-nitrophenylphosphatase activity in the somatosensory cortex of the rat.Journal of Histochemistry & Cytochemistry, 1976
- Production and role of inner ear fluidProgress in Neurobiology, 1975
- Histochemical demonstration of (Na+ + K+)-activated ATPase activity of synaptosomes and synaptosomal membranesExperimental Neurology, 1975
- The Effects of Sodium and Potassium on Ouabain Binding by Human ErythrocytesThe Journal of general physiology, 1972
- Adenosine Triphosphatase Distribution in the Organ of Corti: Histochemical Study by Light and Electron MicroscopyActa Oto-Laryngologica, 1967