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Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging

The radial localization and properties of elementary calcium release events (“puffs”) were studied in Xenopus oocytes using a confocal microscope equipped with a piezoelectric focussing unit to allow rapid (>100 Hz) imaging of calcium signals along a radial line into the cell with a spatial resol...

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Detalles Bibliográficos
Autores principales: Callamaras, Nick, Parker, Ian
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2223371/
https://www.ncbi.nlm.nih.gov/pubmed/9925819
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author Callamaras, Nick
Parker, Ian
author_facet Callamaras, Nick
Parker, Ian
author_sort Callamaras, Nick
collection PubMed
description The radial localization and properties of elementary calcium release events (“puffs”) were studied in Xenopus oocytes using a confocal microscope equipped with a piezoelectric focussing unit to allow rapid (>100 Hz) imaging of calcium signals along a radial line into the cell with a spatial resolution of <0.7 μm. Weak photorelease of caged inositol 1,4,5-trisphosphate (InsP (3)) evoked puffs arising predominantly within a 6-μm thick band located within a few micrometers of the cell surface. Approximately 25% of puffs had a restricted radial spread, consistent with calcium release from a single site. Most puffs, however, exhibited a greater radial spread (3.25 μm), likely involving recruitment of radially neighboring release sites. Calcium waves evoked by just suprathreshold stimuli exhibited radial calcium distributions consistent with inward diffusion of calcium liberated at puff sites, whereas stronger flashes evoked strong, short-latency signals at depths inward from puff sites, indicating deep InsP (3)-sensitive stores activated at higher concentrations of InsP (3). Immunolocalization of InsP (3) receptors showed punctate staining throughout a region corresponding to the localization of puffs and subplasmalemmal endoplasmic reticulum. The radial organization of puff sites a few micrometers inward from the plasma membrane may have important consequences for activation of calcium-dependent ion channels and “capacitative” calcium influx. However, on the macroscopic (hundreds of micrometers) scale of global calcium waves, release can be considered to occur primarily within a thin, essentially two-dimensional subplasmalemmal shell.
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spelling pubmed-22233712008-04-21 Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging Callamaras, Nick Parker, Ian J Gen Physiol Article The radial localization and properties of elementary calcium release events (“puffs”) were studied in Xenopus oocytes using a confocal microscope equipped with a piezoelectric focussing unit to allow rapid (>100 Hz) imaging of calcium signals along a radial line into the cell with a spatial resolution of <0.7 μm. Weak photorelease of caged inositol 1,4,5-trisphosphate (InsP (3)) evoked puffs arising predominantly within a 6-μm thick band located within a few micrometers of the cell surface. Approximately 25% of puffs had a restricted radial spread, consistent with calcium release from a single site. Most puffs, however, exhibited a greater radial spread (3.25 μm), likely involving recruitment of radially neighboring release sites. Calcium waves evoked by just suprathreshold stimuli exhibited radial calcium distributions consistent with inward diffusion of calcium liberated at puff sites, whereas stronger flashes evoked strong, short-latency signals at depths inward from puff sites, indicating deep InsP (3)-sensitive stores activated at higher concentrations of InsP (3). Immunolocalization of InsP (3) receptors showed punctate staining throughout a region corresponding to the localization of puffs and subplasmalemmal endoplasmic reticulum. The radial organization of puff sites a few micrometers inward from the plasma membrane may have important consequences for activation of calcium-dependent ion channels and “capacitative” calcium influx. However, on the macroscopic (hundreds of micrometers) scale of global calcium waves, release can be considered to occur primarily within a thin, essentially two-dimensional subplasmalemmal shell. The Rockefeller University Press 1999-02-01 /pmc/articles/PMC2223371/ /pubmed/9925819 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Callamaras, Nick
Parker, Ian
Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title_full Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title_fullStr Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title_full_unstemmed Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title_short Radial Localization of Inositol 1,4,5-Trisphosphate–sensitive Ca(2+) Release Sites in Xenopus Oocytes Resolved by Axial Confocal Linescan Imaging
title_sort radial localization of inositol 1,4,5-trisphosphate–sensitive ca(2+) release sites in xenopus oocytes resolved by axial confocal linescan imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2223371/
https://www.ncbi.nlm.nih.gov/pubmed/9925819
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