Theoretical analysis of the Ca2+ spark amplitude distribution

被引:67
作者
Izu, LT
Wier, WG
Balke, CW
机构
[1] Univ Maryland, Sch Med, Dept Physiol, Baltimore, MD 21201 USA
[2] Univ Maryland, Sch Med, Dept Med, Div Cardiol, Baltimore, MD 21201 USA
关键词
D O I
10.1016/S0006-3495(98)74034-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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 fluo3 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 Ca2+-bound fluo-3 is Gaussian, we show the following: I)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.
引用
收藏
页码:1144 / 1162
页数:19
相关论文
共 37 条
[1]   PROCESSES THAT REMOVE CALCIUM FROM THE CYTOPLASM DURING EXCITATION-CONTRACTION COUPLING IN INTACT RAT-HEART CELLS [J].
BALKE, CW ;
EGAN, TM ;
WIER, WG .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 474 (03) :447-462
[2]   INTRINSIC CYTOSOLIC CALCIUM BUFFERING PROPERTIES OF SINGLE-RAT CARDIAC MYOCYTES [J].
BERLIN, JR ;
BASSANI, JWM ;
BERS, DM .
BIOPHYSICAL JOURNAL, 1994, 67 (04) :1775-1787
[3]   INTRACELLULAR DIFFUSION, BINDING, AND COMPARTMENTALIZATION OF THE FLUORESCENT CALCIUM INDICATORS INDO-1 AND FURA-2 [J].
BLATTER, LA ;
WIER, WG .
BIOPHYSICAL JOURNAL, 1990, 58 (06) :1491-1499
[4]   Sarcoplasmic reticulum Ca2+ release flux underlying Ca2+ sparks in cardiac muscle [J].
Blatter, LA ;
Huser, J ;
Rios, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :4176-4181
[5]   THE CONTROL OF CALCIUM-RELEASE IN HEART-MUSCLE [J].
CANNELL, MB ;
CHENG, H ;
LEDERER, WJ .
SCIENCE, 1995, 268 (5213) :1045-1049
[6]   CALCIUM SPARKS - ELEMENTARY EVENTS UNDERLYING EXCITATION-CONTRACTION COUPLING IN HEART-MUSCLE [J].
CHENG, H ;
LEDERER, WJ ;
CANNELL, MB .
SCIENCE, 1993, 262 (5134) :740-744
[7]   Ca2+ diffusion and sarcoplasmic reticulum transport both contribute to [Ca2+](i) decline during Ca2+ sparks in rat ventricular myocytes [J].
Gomez, AM ;
Cheng, HP ;
Lederer, WJ ;
Bers, DM .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 496 (02) :575-581
[8]  
Gyorke S, 1997, J PHYSIOL-LONDON, V500, P297
[9]  
Hague D. N., 1977, CHEM RELAXATION MOL, P84
[10]   RESTING MYOPLASMIC FREE CALCIUM IN FROG SKELETAL-MUSCLE FIBERS ESTIMATED WITH FLUO-3 [J].
HARKINS, AB ;
KUREBAYASHI, N ;
BAYLOR, SM .
BIOPHYSICAL JOURNAL, 1993, 65 (02) :865-881