Dynamic local changes in sarcoplasmic reticulum calcium: physiological and pathophysiological roles.

Evidence obtained in recent years indicates that, in cardiac myocytes, release of Ca(2+) from the sarcoplasmic reticulum (SR) is regulated by changes in the concentration of Ca(2+) within the SR. In this review, we summarize recent advances in our understanding of this regulatory role, with a particular emphasis on dynamic and local changes in SR [Ca(2+)]. We focus on five important questions that are to some extent unresolved and controversial. These questions concern: (1) the importance of SR [Ca(2+)] depletion in the termination of Ca(2+) release; (2) the quantitative extent of depletion during local release events such as Ca(2+) sparks; (3) the influence of SR [Ca(2+)] refilling on release refractoriness and the propensity for pathological Ca(2+) release; (4) dynamic changes in SR [Ca(2+)] during propagating Ca(2+) waves; and (5) the speed of Ca(2+) diffusion within the SR. With each issue, we discuss data supporting alternative viewpoints, and we identify fundamental questions that are being actively investigated. We conclude with a discussion of experimental and computational advances that will help to resolve controversies. This article is part of a special issue entitled "Local Signaling in Myocytes."

[1]  Sandor Györke,et al.  The role of luminal Ca2+ in the generation of Ca2+ waves in rat ventricular myocytes , 1999, The Journal of physiology.

[2]  Donald M. Bers,et al.  Ca2+ Scraps: Local Depletions of Free [Ca2+] in Cardiac Sarcoplasmic Reticulum During Contractions Leave Substantial Ca2+ Reserve , 2003, Circulation research.

[3]  D. Roden,et al.  Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia. , 2006, The Journal of clinical investigation.

[4]  Donald M Bers,et al.  Sarcoplasmic Reticulum and Nuclear Envelope Are One Highly Interconnected Ca2+ Store Throughout Cardiac Myocyte , 2006, Circulation research.

[5]  W. Lederer,et al.  The control of calcium release in heart muscle. , 1995, Science.

[6]  Heping Cheng,et al.  Putting out the fire: what terminates calcium-induced calcium release in cardiac muscle? , 2004, Cell calcium.

[7]  S Coombes,et al.  A bidomain threshold model of propagating calcium waves , 2008, Journal of mathematical biology.

[8]  Heping Cheng,et al.  Polymorphism of Ca2+ sparks evoked from in-focus Ca2+ release units in cardiac myocytes. , 2004, Biophysical journal.

[9]  M. Diaz,et al.  Sarcoplasmic Reticulum Calcium Content Fluctuation Is the Key to Cardiac Alternans , 2004, Circulation research.

[10]  M. Cannell,et al.  Allosteric activation of Na+-Ca2+ exchange by L-type Ca2+ current augments the trigger flux for SR Ca2+ release in ventricular myocytes. , 2008, Biophysical journal.

[11]  W. Lederer,et al.  Calcium Sparks and Excitation–Contraction Coupling in Phospholamban‐Deficient Mouse Ventricular Myocytes , 1997, The Journal of physiology.

[12]  M. Diaz,et al.  Measurement of sarcoplasmic reticulum Ca2+ content and sarcolemmal Ca2+ fluxes in isolated rat ventricular myocytes during spontaneous Ca2+ release , 1997, The Journal of physiology.

[13]  M. Cannell,et al.  Local control in cardiac E-C coupling. , 2012, Journal of molecular and cellular cardiology.

[14]  Stephen Coombes,et al.  Calcium signalling during excitation-contraction coupling in mammalian atrial myocytes , 2006, Journal of Cell Science.

[15]  C. Ward,et al.  Subcellular Ca2+ signaling in the heart: the role of ryanodine receptor sensitivity , 2010, The Journal of general physiology.

[16]  D. Bers,et al.  Potentiation of fractional sarcoplasmic reticulum calcium release by total and free intra-sarcoplasmic reticulum calcium concentration. , 2000, Biophysical journal.

[17]  S. Priori,et al.  Unexpected Structural and Functional Consequences of the R33Q Homozygous Mutation in Cardiac Calsequestrin: A Complex Arrhythmogenic Cascade in a Knock In Mouse Model , 2008, Circulation research.

[18]  Alan Garfinkel,et al.  Spark-Induced Sparks As a Mechanism of Intracellular Calcium Alternans in Cardiac Myocytes , 2010, Circulation research.

[19]  Katherine A. Sheehan,et al.  Local calcium gradients during excitation–contraction coupling and alternans in atrial myocytes , 2003, The Journal of physiology.

[20]  W. Lederer,et al.  Calcium sparks and [Ca2+]i waves in cardiac myocytes. , 1996, The American journal of physiology.

[21]  D. Terentyev,et al.  Luminal Ca2+ Controls Termination and Refractory Behavior of Ca2+-Induced Ca2+ Release in Cardiac Myocytes , 2002, Circulation research.

[22]  E. Ríos,et al.  Unitary Ca2+ Current through Mammalian Cardiac and Amphibian Skeletal Muscle Ryanodine Receptor Channels under Near-physiological Ionic Conditions , 2003, The Journal of general physiology.

[23]  Donald M. Bers,et al.  Excitation-Contraction Coupling and Cardiac Contractile Force , 1991, Developments in Cardiovascular Medicine.

[24]  Petter Laake,et al.  T‐tubule disorganization and reduced synchrony of Ca2+ release in murine cardiomyocytes following myocardial infarction , 2006, The Journal of physiology.

[25]  Dmitry Terentyev,et al.  Modulation of SR Ca release by luminal Ca and calsequestrin in cardiac myocytes: effects of CASQ2 mutations linked to sudden cardiac death. , 2008, Biophysical journal.

[26]  A. J. Williams,et al.  Evidence for Ca(2+) activation and inactivation sites on the luminal side of the cardiac ryanodine receptor complex. , 2000, Circulation research.

[27]  Eric A Sobie,et al.  Moment closure for local control models of calcium-induced calcium release in cardiac myocytes. , 2008, Biophysical journal.

[28]  Heping Cheng,et al.  RyR2 mutations linked to ventricular tachycardia and sudden death reduce the threshold for store-overload-induced Ca2+ release (SOICR). , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[29]  Eric A. Sobie,et al.  Regression Analysis for Constraining Free Parameters in Electrophysiological Models of Cardiac Cells , 2009, PLoS Comput. Biol..

[30]  W. Lederer,et al.  The Ca2+ leak paradox and “rogue ryanodine receptors”: SR Ca2+ efflux theory and practice , 2006 .

[31]  D. Bers Cardiac excitation–contraction coupling , 2002, Nature.

[32]  Donald M Bers,et al.  Regulation of cardiac sarcoplasmic reticulum Ca release by luminal [Ca] and altered gating assessed with a mathematical model. , 2005, Biophysical journal.

[33]  D. Laver Ca2+ stores regulate ryanodine receptor Ca2+ release channels via luminal and cytosolic Ca2+ sites. , 2007, Biophysical journal.

[34]  M. Stern,et al.  Calcium-dependent Inactivation Terminates Calcium Release in Skeletal Muscle of Amphibians , 2008, The Journal of general physiology.

[35]  A. Garfinkel,et al.  Alternans and Arrhythmias: From Cell to Heart , 2011, Circulation research.

[36]  E. Sobie Parameter sensitivity analysis in electrophysiological models using multivariable regression. , 2009, Biophysical journal.

[37]  J. Shadid,et al.  Interplay of ryanodine receptor distribution and calcium dynamics. , 2006, Biophysical journal.

[38]  Eric A Sobie,et al.  Termination of cardiac Ca(2+) sparks: an investigative mathematical model of calcium-induced calcium release. , 2002, Biophysical journal.

[39]  Godfrey L. Smith,et al.  Assessment of sarcoplasmic reticulum Ca2+ depletion during spontaneous Ca2+ waves in isolated permeabilized rabbit ventricular cardiomyocytes. , 2009, Biophysical journal.

[40]  S. Huke,et al.  Ablation of triadin causes loss of cardiac Ca2+ release units, impaired excitation–contraction coupling, and cardiac arrhythmias , 2009, Proceedings of the National Academy of Sciences.

[41]  M. Diaz,et al.  Coordinated Control of Cell Ca 2 1 Loading and Triggered Release From the Sarcoplasmic Reticulum Underlies the Rapid Inotropic Response to Increased L-Type Ca 2 1 Current , 2001 .

[42]  Huihui Kong,et al.  Enhanced Store Overload–Induced Ca2+ Release and Channel Sensitivity to Luminal Ca2+ Activation Are Common Defects of RyR2 Mutations Linked to Ventricular Tachycardia and Sudden Death , 2005, Circulation research.

[43]  Pawel Swietach,et al.  Modeling calcium waves in cardiac myocytes: importance of calcium diffusion. , 2010, Frontiers in Bioscience.

[44]  W. Lederer,et al.  Calcium sparks: elementary events underlying excitation-contraction coupling in heart muscle. , 1993, Science.

[45]  E. Sobie,et al.  Complex and rate-dependent beat-to-beat variations in Ca2+ transients of canine Purkinje cells. , 2011, Journal of molecular and cellular cardiology.

[46]  D. Bers,et al.  Quantitative Assessment of the SR Ca2+ Leak-Load Relationship , 2002, Circulation research.

[47]  Clara Franzini-Armstrong,et al.  Ca2+ blinks: rapid nanoscopic store calcium signaling. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[48]  C W Balke,et al.  Ca(2+) release mechanisms, Ca(2+) sparks, and local control of excitation-contraction coupling in normal heart muscle. , 1999, Circulation research.

[49]  J. Seidman,et al.  Calsequestrin 2 (CASQ2) mutations increase expression of calreticulin and ryanodine receptors, causing catecholaminergic polymorphic ventricular tachycardia. , 2007, The Journal of clinical investigation.

[50]  C. Yin,et al.  Ryanodine receptor arrays: not just a pretty pattern? , 2008, Trends in cell biology.

[51]  M. Egger,et al.  Sarcoplasmic Reticulum Ca2+ Refilling Controls Recovery From Ca2+-Induced Ca2+ Release Refractoriness in Heart Muscle , 2004, Circulation research.

[52]  Willem Flameng,et al.  Reduced synchrony of Ca2+ release with loss of T-tubules-a comparison to Ca2+ release in human failing cardiomyocytes. , 2004, Cardiovascular research.

[53]  D. Allen,et al.  The use of the indicator fluo‐5N to measure sarcoplasmic reticulum calcium in single muscle fibres of the cane toad , 2001, The Journal of physiology.

[54]  Pawel Swietach,et al.  Ca2+-mobility in the sarcoplasmic reticulum of ventricular myocytes is low. , 2008, Biophysical journal.

[55]  Eric A Sobie,et al.  Excitation–contraction coupling gain in ventricular myocytes: insights from a parsimonious model , 2009, The Journal of physiology.

[56]  Sandor Györke,et al.  The role of calsequestrin, triadin, and junctin in conferring cardiac ryanodine receptor responsiveness to luminal calcium. , 2004, Biophysical journal.

[57]  Cardiac Excitation–Contraction Coupling , 2013 .

[58]  F. Protasi,et al.  Shape, size, and distribution of Ca(2+) release units and couplons in skeletal and cardiac muscles. , 1999, Biophysical journal.

[59]  D. Terentyev,et al.  Protein–protein interactions between triadin and calsequestrin are involved in modulation of sarcoplasmic reticulum calcium release in cardiac myocytes , 2007, The Journal of physiology.

[60]  Isuru D. Jayasinghe,et al.  Optical single-channel resolution imaging of the ryanodine receptor distribution in rat cardiac myocytes , 2009, Proceedings of the National Academy of Sciences.

[61]  Ernst Niggli,et al.  Calcium signalling in cardiac muscle: refractoriness revealed by coherent activation , 1999, Nature Cell Biology.

[62]  W Yuan,et al.  Fractional SR Ca release is regulated by trigger Ca and SR Ca content in cardiac myocytes. , 1995, The American journal of physiology.

[63]  S. Priori,et al.  Abnormal Interactions of Calsequestrin With the Ryanodine Receptor Calcium Release Channel Complex Linked to Exercise-Induced Sudden Cardiac Death , 2006, Circulation research.

[64]  S. Priori,et al.  Luminal Ca2+ Regulation of Single Cardiac Ryanodine Receptors: Insights Provided by Calsequestrin and its Mutants , 2008, The Journal of general physiology.

[65]  Eduardo Ríos,et al.  The quantal nature of Ca2+ sparks and in situ operation of the ryanodine receptor array in cardiac cells. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[66]  Christopher W. Ward,et al.  Time Course of Individual Ca2+ Sparks in Frog Skeletal Muscle Recorded at High Time Resolution , 1999, The Journal of general physiology.

[67]  Eric A Sobie,et al.  Recovery of cardiac calcium release is controlled by sarcoplasmic reticulum refilling and ryanodine receptor sensitivity. , 2011, Cardiovascular research.

[68]  W. Lederer,et al.  Quarky Calcium Release in the Heart , 2011, Circulation research.

[69]  Eric A Sobie,et al.  Orphaned ryanodine receptors in the failing heart. , 2006, Proceedings of the National Academy of Sciences of the United States of America.

[70]  S. Priori,et al.  Abnormal Calcium Signaling and Sudden Cardiac Death Associated With Mutation of Calsequestrin , 2004, Circulation research.

[71]  N. Torres,et al.  Na+ currents are required for efficient excitation–contraction coupling in rabbit ventricular myocytes: a possible contribution of neuronal Na+ channels , 2010, The Journal of physiology.

[72]  D Noble,et al.  A meta‐analysis of cardiac electrophysiology computational models , 2009, Experimental physiology.

[73]  Donald M. Bers,et al.  Termination of Cardiac Ca2+ Sparks: Role of Intra-SR [Ca2+], Release Flux, and Intra-SR Ca2+ Diffusion , 2008, Circulation research.

[74]  N. Macquaide,et al.  Dyssynchrony of Ca2+ release from the sarcoplasmic reticulum as subcellular mechanism of cardiac contractile dysfunction. , 2011, Journal of molecular and cellular cardiology.

[75]  Eric A Sobie,et al.  Local recovery of Ca2+ release in rat ventricular myocytes , 2005, The Journal of physiology.

[76]  Godfrey L. Smith,et al.  Measurement and modeling of Ca2+ waves in isolated rabbit ventricular cardiomyocytes. , 2007, Biophysical journal.

[77]  Donald M Bers,et al.  Cardiac Alternans Do Not Rely on Diastolic Sarcoplasmic Reticulum Calcium Content Fluctuations , 2006, Circulation research.

[78]  Joseph L Greenstein,et al.  Role of CaMKII in RyR leak, EC coupling and action potential duration: a computational model. , 2010, Journal of molecular and cellular cardiology.

[79]  W. Giles,et al.  Location of the initiation site of calcium transients and sparks in rabbit heart Purkinje cells , 2001, The Journal of physiology.

[80]  Eric A Sobie,et al.  Spontaneous Ca2+ sparks and Ca2+ homeostasis in a minimal model of permeabilized ventricular myocytes. , 2010, American journal of physiology. Heart and circulatory physiology.

[81]  Michael J. Holst,et al.  Numerical Analysis of Ca2+ Signaling in Rat Ventricular Myocytes with Realistic Transverse-Axial Tubular Geometry and Inhibited Sarcoplasmic Reticulum , 2010, PLoS Comput. Biol..

[82]  Christian Soeller,et al.  Three-dimensional distribution of ryanodine receptor clusters in cardiac myocytes. , 2006, Biophysical journal.

[83]  Karin Sipido,et al.  Remodeling of T-Tubules and Reduced Synchrony of Ca2+ Release in Myocytes From Chronically Ischemic Myocardium , 2008, Circulation research.

[84]  A. Di Maio,et al.  Di Maio, A , 2012 .

[85]  I. Györke,et al.  Regulation of the cardiac ryanodine receptor channel by luminal Ca2+ involves luminal Ca2+ sensing sites. , 1998, Biophysical journal.

[86]  Donald M Bers,et al.  Partial inhibition of sarcoplasmic reticulum ca release evokes long-lasting ca release events in ventricular myocytes: role of luminal ca in termination of ca release. , 2008, Biophysical journal.

[87]  Dmitry Terentyev,et al.  Calsequestrin determines the functional size and stability of cardiac intracellular calcium stores: Mechanism for hereditary arrhythmia , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[88]  D. Rosenbaum,et al.  Cellular mechanisms of arrhythmogenic cardiac alternans. , 2008, Progress in biophysics and molecular biology.

[89]  Joseph L Greenstein,et al.  Mechanisms of excitation-contraction coupling in an integrative model of the cardiac ventricular myocyte. , 2006, Biophysical journal.

[90]  Eric A Sobie,et al.  Predicting local SR Ca(2+) dynamics during Ca(2+) wave propagation in ventricular myocytes. , 2010, Biophysical journal.

[91]  Alan Garfinkel,et al.  Intracellular Ca alternans: coordinated regulation by sarcoplasmic reticulum release, uptake, and leak. , 2008, Biophysical journal.

[92]  A. Trafford,et al.  What role does modulation of the ryanodine receptor play in cardiac inotropy and arrhythmogenesis? , 2009, Journal of molecular and cellular cardiology.

[93]  Y. Shiferaw,et al.  Variability in Timing of Spontaneous Calcium Release in the Intact Rat Heart Is Determined by the Time Course of Sarcoplasmic Reticulum Calcium Load , 2010, Circulation research.

[94]  Dmitry Terentyev,et al.  Intra‐sarcoplasmic reticulum Ca2+ oscillations are driven by dynamic regulation of ryanodine receptor function by luminal Ca2+ in cardiomyocytes , 2009, The Journal of physiology.

[95]  Donald M Bers,et al.  Dynamic Calcium Movement Inside Cardiac Sarcoplasmic Reticulum During Release , 2011, Circulation research.

[96]  C W Balke,et al.  Local calcium transients triggered by single L-type calcium channel currents in cardiac cells. , 1995, Science.

[97]  D. Bers,et al.  Ca2+ diffusion and sarcoplasmic reticulum transport both contribute to [Ca2+]i decline during Ca2+ sparks in rat ventricular myocytes. , 1996, The Journal of physiology.

[98]  M. Diaz,et al.  Modulation of CICR has no maintained effect on systolic Ca2+: simultaneous measurements of sarcoplasmic reticulum and sarcolemmal Ca2+ fluxes in rat ventricular myocytes , 2000, The Journal of physiology.

[99]  Juan G Restrepo,et al.  Positive Feedback Mechanisms among Local Ca Releases, NCX, and ICaL Ignite Pacemaker Action Potentials. , 2018, Biophysical journal.