Cargando…

Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle

An algorithm for the calculation of Ca(2+) release flux underlying Ca(2+) sparks (Blatter, L.A., J. Hüser, and E. Ríos. 1997. Proc. Natl. Acad. Sci. USA. 94:4176–4181) was modified and applied to sparks obtained by confocal microscopy in single frog skeletal muscle fibers, which were voltage clamped...

Descripción completa

Detalles Bibliográficos
Autores principales: Ríos, Eduardo, Stern, Michael D., González, Adom, Pizarro, Gonzalo, Shirokova, Natalia
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2229636/
https://www.ncbi.nlm.nih.gov/pubmed/10398690
_version_ 1782150174396645376
author Ríos, Eduardo
Stern, Michael D.
González, Adom
Pizarro, Gonzalo
Shirokova, Natalia
author_facet Ríos, Eduardo
Stern, Michael D.
González, Adom
Pizarro, Gonzalo
Shirokova, Natalia
author_sort Ríos, Eduardo
collection PubMed
description An algorithm for the calculation of Ca(2+) release flux underlying Ca(2+) sparks (Blatter, L.A., J. Hüser, and E. Ríos. 1997. Proc. Natl. Acad. Sci. USA. 94:4176–4181) was modified and applied to sparks obtained by confocal microscopy in single frog skeletal muscle fibers, which were voltage clamped in a two-Vaseline gap chamber or permeabilized and immersed in fluo-3–containing internal solution. The performance of the algorithm was characterized on sparks obtained by simulation of fluorescence due to release of Ca(2+) from a spherical source, in a homogeneous three-dimensional space that contained components representing cytoplasmic molecules and Ca(2+) removal processes. Total release current, as well as source diameter and noise level, was varied in the simulations. Derived release flux or current, calculated by volume integration of the derived flux density, estimated quite closely the current used in the simulation, while full width at half magnitude of the derived release flux was a good monitor of source size only at diameters >0.7 μm. On an average of 157 sparks of amplitude >2 U resting fluorescence, located automatically in a representative voltage clamp experiment, the algorithm reported a release current of 16.9 pA, coming from a source of 0.5 μm, with an open time of 6.3 ms. Fewer sparks were obtained in permeabilized fibers, so that the algorithm had to be applied to individual sparks or averages of few events, which degraded its performance in comparable tests. The average current reported for 19 large sparks obtained in permeabilized fibers was 14.4 pA. A minimum estimate, derived from the rate of change of dye-bound Ca(2+) concentration, was 8 pA. Such a current would require simultaneous opening of between 8 and 60 release channels with unitary Ca(2+) currents of the level recorded in bilayer experiments. Real sparks differ from simulated ones mainly in having greater width. Correspondingly, the algorithm reported greater spatial extent of the source for real sparks. This may again indicate a multichannel origin of sparks, or could reflect limitations in spatial resolution.
format Text
id pubmed-2229636
institution National Center for Biotechnology Information
language English
publishDate 1999
publisher The Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-22296362008-04-22 Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle Ríos, Eduardo Stern, Michael D. González, Adom Pizarro, Gonzalo Shirokova, Natalia J Gen Physiol Original Article An algorithm for the calculation of Ca(2+) release flux underlying Ca(2+) sparks (Blatter, L.A., J. Hüser, and E. Ríos. 1997. Proc. Natl. Acad. Sci. USA. 94:4176–4181) was modified and applied to sparks obtained by confocal microscopy in single frog skeletal muscle fibers, which were voltage clamped in a two-Vaseline gap chamber or permeabilized and immersed in fluo-3–containing internal solution. The performance of the algorithm was characterized on sparks obtained by simulation of fluorescence due to release of Ca(2+) from a spherical source, in a homogeneous three-dimensional space that contained components representing cytoplasmic molecules and Ca(2+) removal processes. Total release current, as well as source diameter and noise level, was varied in the simulations. Derived release flux or current, calculated by volume integration of the derived flux density, estimated quite closely the current used in the simulation, while full width at half magnitude of the derived release flux was a good monitor of source size only at diameters >0.7 μm. On an average of 157 sparks of amplitude >2 U resting fluorescence, located automatically in a representative voltage clamp experiment, the algorithm reported a release current of 16.9 pA, coming from a source of 0.5 μm, with an open time of 6.3 ms. Fewer sparks were obtained in permeabilized fibers, so that the algorithm had to be applied to individual sparks or averages of few events, which degraded its performance in comparable tests. The average current reported for 19 large sparks obtained in permeabilized fibers was 14.4 pA. A minimum estimate, derived from the rate of change of dye-bound Ca(2+) concentration, was 8 pA. Such a current would require simultaneous opening of between 8 and 60 release channels with unitary Ca(2+) currents of the level recorded in bilayer experiments. Real sparks differ from simulated ones mainly in having greater width. Correspondingly, the algorithm reported greater spatial extent of the source for real sparks. This may again indicate a multichannel origin of sparks, or could reflect limitations in spatial resolution. The Rockefeller University Press 1999-07-01 /pmc/articles/PMC2229636/ /pubmed/10398690 Text en © 1999 The Rockefeller University Press 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 Original Article
Ríos, Eduardo
Stern, Michael D.
González, Adom
Pizarro, Gonzalo
Shirokova, Natalia
Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title_full Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title_fullStr Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title_full_unstemmed Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title_short Calcium Release Flux Underlying Ca(2+) Sparks of Frog Skeletal Muscle
title_sort calcium release flux underlying ca(2+) sparks of frog skeletal muscle
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2229636/
https://www.ncbi.nlm.nih.gov/pubmed/10398690
work_keys_str_mv AT rioseduardo calciumreleasefluxunderlyingca2sparksoffrogskeletalmuscle
AT sternmichaeld calciumreleasefluxunderlyingca2sparksoffrogskeletalmuscle
AT gonzalezadom calciumreleasefluxunderlyingca2sparksoffrogskeletalmuscle
AT pizarrogonzalo calciumreleasefluxunderlyingca2sparksoffrogskeletalmuscle
AT shirokovanatalia calciumreleasefluxunderlyingca2sparksoffrogskeletalmuscle