Literature DB >> 9726917

Theoretical analysis of the Ca2+ spark amplitude distribution.

L T Izu1, W G Wier, C W Balke.   

Abstract

A difficulty of using confocal microscopy to study Ca2+ sparks is the uncertainty of the linescan position with respect to the source of Ca2+ release. Random placement of the linescan is expected to result in a broad distribution of measured Ca2+ spark amplitudes (a) even if all Ca2+ sparks were generated identically. Thus variations in Ca2+ spark amplitude due to positional differences between confocal linescans and Ca2+ release site are intertwined with variations due to intrinsic differences in Ca2+ release properties. To separate these two sources of variations on the Ca2+ spark amplitude, we determined the effect changes of channel current or channel open time--collectively called the source strength, alpha--had on the measured Ca2+ spark amplitude histogram, N(a). This was done by 1) simulating Ca2+ release, Ca2+ and fluo-3 diffusion, and Ca2+ binding reactions; 2) simulation of image formation of the Ca2+ spark by a confocal microscope; and 3) using a novel automatic Ca2+ spark detector. From these results we derived an integral equation relating the probability density function of source strengths, f alpha (alpha), to N(a), which takes into account random positional variations between the source and linescan. In the special, but important, case that the spatial distribution of Ca(2+)-bound fluo-3 is Gaussian, we show the following: 1) variations of Ca2+ spark amplitude due to positional or intrinsic differences can be separated, and 2) f alpha (alpha) can, in principle, be calculated from the Ca2+ spark amplitude histogram since N(a) is the sum of shifted hyperbolas, where the magnitudes of the shifts and weights depend on f alpha (alpha). In particular, if all Ca2+ sparks were generated identically, then the plot of 1/N(a) against a will be a straight line. Multiple populations of channels carrying distinct currents are revealed by discontinuities in the 1/N(a) plot. 3) Although the inverse relationship between Ca2+ spark amplitude and decay time might be used to distinguish Ca2+ sparks from different channel populations, noise can render the measured decay times meaningless for small amplitude Ca2+ sparks.

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Year:  1998        PMID: 9726917      PMCID: PMC1299790          DOI: 10.1016/s0006-3495(98)74034-2

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  32 in total

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Authors:  S R Shorofsky; L Izu; W G Wier; C W Balke
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2.  Partial depletion of sarcoplasmic reticulum calcium does not prevent calcium sparks in rat ventricular myocytes.

Authors:  L S Song; M D Stern; E G Lakatta; H Cheng
Journal:  J Physiol       Date:  1997-12-15       Impact factor: 5.182

3.  A high-resolution, confocal laser-scanning microscope and flash photolysis system for physiological studies.

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4.  Small event Ca2+ release: a probable precursor of Ca2+ sparks in frog skeletal muscle.

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Journal:  J Physiol       Date:  1997-07-01       Impact factor: 5.182

5.  Ca2+ 'sparks' and waves in intact ventricular muscle resolved by confocal imaging.

Authors:  W G Wier; H E ter Keurs; E Marban; W D Gao; C W Balke
Journal:  Circ Res       Date:  1997-10       Impact factor: 17.367

6.  Effects of [Ca2+]i, SR Ca2+ load, and rest on Ca2+ spark frequency in ventricular myocytes.

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9.  Factors shaping the confocal image of the calcium spark in cardiac muscle cells.

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  40 in total

1.  Large currents generate cardiac Ca2+ sparks.

Authors:  L T Izu; J R Mauban; C W Balke; W G Wier
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

2.  A preferred amplitude of calcium sparks in skeletal muscle.

Authors:  E Ríos; N Shirokova; W G Kirsch; G Pizarro; M D Stern; H Cheng; A González
Journal:  Biophys J       Date:  2001-01       Impact factor: 4.033

3.  Involvement of multiple intracellular release channels in calcium sparks of skeletal muscle.

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4.  Estimation of the sarcoplasmic reticulum Ca2+ release flux underlying Ca2+ sparks.

Authors:  Christian Soeller; Mark B Cannell
Journal:  Biophys J       Date:  2002-05       Impact factor: 4.033

5.  Polymorphism of Ca2+ sparks evoked from in-focus Ca2+ release units in cardiac myocytes.

Authors:  Jian-Xin Shen; ShiQiang Wang; Long-Sheng Song; Taizhen Han; Heping Cheng
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

6.  Thermodynamically irreversible gating of ryanodine receptors in situ revealed by stereotyped duration of release in Ca(2+) sparks.

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Journal:  Biophys J       Date:  2002-07       Impact factor: 4.033

7.  Stochastic properties of Ca(2+) release of inositol 1,4,5-trisphosphate receptor clusters.

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Journal:  Biophys J       Date:  2002-07       Impact factor: 4.033

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9.  Theory and applications of geometric scaling of localized calcium release events.

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Journal:  Am J Physiol Cell Physiol       Date:  2010-08-11       Impact factor: 4.249

10.  A Novel Technique of Quantifying Flexural Stiffness of Rod-Like Structures.

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Journal:  Cell Mol Bioeng       Date:  2008-03-18       Impact factor: 2.321

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