An algorithm for the calculation of Ca2+ release flux underlying Ca2+ 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 Ca2+ from a spherical source, in a homogeneous three-dimensional space that contained components representing cytoplasmic molecules and Ca2+ 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 Ca2+ concentration, was 8 pA. Such a current would require simultaneous opening of between 8 and 60 release channels with unitary Ca2+ 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.
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1 July 1999
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July 01 1999
Calcium Release Flux Underlying Ca2+ Sparks of Frog Skeletal Muscle
Eduardo Ríos,
Eduardo Ríos
aFrom the Department of Molecular Biophysics and Physiology, Rush University, Chicago, Illinois 60612
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Michael D. Stern,
Michael D. Stern
bLaboratory of Cardiovascular Science, Gerontology Research Center, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224
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Gonzalo Pizarro,
Gonzalo Pizarro
cDepartamento de Biofísica, Facultad de Medicina, Universidad de la República, G. Flores 2125, Montevideo, Uruguay
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Natalia Shirokova
Natalia Shirokova
aFrom the Department of Molecular Biophysics and Physiology, Rush University, Chicago, Illinois 60612
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Eduardo Ríos
aFrom the Department of Molecular Biophysics and Physiology, Rush University, Chicago, Illinois 60612
Michael D. Stern
bLaboratory of Cardiovascular Science, Gerontology Research Center, National Institute on Aging, National Institutes of Health, Baltimore, Maryland 21224
Adom González
Gonzalo Pizarro
cDepartamento de Biofísica, Facultad de Medicina, Universidad de la República, G. Flores 2125, Montevideo, Uruguay
Natalia Shirokova
aFrom the Department of Molecular Biophysics and Physiology, Rush University, Chicago, Illinois 60612
1used in this paper: FDHM, full duration at half magnitude; FWHM, full width at half magnitude; PSF, point spread function; SR, sarcoplasmic reticulum
Dr. Shirokova's permanent address is A.A. Bogomoletz Institute of Physiology, Bogomoletz St. 4, Kiev, Ukraine.
Received:
October 13 1998
Revision Requested:
May 07 1999
Accepted:
May 10 1999
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 1999 The Rockefeller University Press
1999
The Rockefeller University Press
J Gen Physiol (1999) 114 (1): 31–48.
Article history
Received:
October 13 1998
Revision Requested:
May 07 1999
Accepted:
May 10 1999
Citation
Eduardo Ríos, Michael D. Stern, Adom González, Gonzalo Pizarro, Natalia Shirokova; Calcium Release Flux Underlying Ca2+ Sparks of Frog Skeletal Muscle. J Gen Physiol 1 July 1999; 114 (1): 31–48. doi: https://doi.org/10.1085/jgp.114.1.31
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