OF WORK The 2D phenomenalogical model has been exercised extensively to generate statistics showing how periodicity of the calcium clock emerges as the RyR calcium release current is increased, allowing the clock to entrain with membrane currents to regulate the heart rate. The results of those simulations have been published in Biophysical Journal. The full Monte-Carlo couplon model with a single cytosolic compartment has been updated to include the effects of local depletion of calcium at individual calcium release terminals of the junctional SR. Simulations of the parallelized model run on Biowulf confirm that local depletion makes a critical contribution to calcium spark termination and that it suffices as the only termination mechanism. However, in that case, there is a critical relationship between the intra-lumenal diffusion rate of SR calcium and the gating kinetics of the RyR that must be satisfied to prevent instability of sparks with delayed termination. Under calcium overload, the single-cytosol couplon model does not osciallate. This makes it clear that it is necessary to use a 3D couplon model to simulate the propagated local releases responsible for calcium clock action. The new 3D algorithm, combining the full couplon model with a spatially resolved cytosolic space using an operator splitting method, has now been completed and demonstrates the local and global propagation of local calcium releases (LCRs) in simulated sino-atrial node cells. The model now explicitly includes coupling to a full set of surface membrane currents, and demonstrates the Lakatta-Maltsev mechanism by which LCRs can drive the spontaneous action potential rhythm of these pacemaker cells. Preliminary results show that this mechanism, together with the presumed role of local SR calcium depletion to terminate release, places significant and previously unrecognized constraints on the placement and clustering of ryanodine receptors in these cells. A more general study of the large parameter space of this model is underway.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIAAG000844-16
Application #
8552484
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
16
Fiscal Year
2012
Total Cost
$432,031
Indirect Cost
Name
National Institute on Aging
Department
Type
DUNS #
City
State
Country
Zip Code
Stern, Michael D; Maltseva, Larissa A; Juhaszova, Magdalena et al. (2014) Hierarchical clustering of ryanodine receptors enables emergence of a calcium clock in sinoatrial node cells. J Gen Physiol 143:577-604
Maltsev, Victor A; Yaniv, Yael; Maltsev, Anna V et al. (2014) Modern perspectives on numerical modeling of cardiac pacemaker cell. J Pharmacol Sci 125:6-38
Stern, Michael D; Ríos, Eduardo; Maltsev, Victor A (2013) Life and death of a cardiac calcium spark. J Gen Physiol 142:257-74
Yaniv, Yael; Stern, Michael D; Lakatta, Edward G et al. (2013) Mechanisms of beat-to-beat regulation of cardiac pacemaker cell function by Ca²⁺ cycling dynamics. Biophys J 105:1551-61
Maltsev, Anna V; Yaniv, Yael; Stern, Michael D et al. (2013) RyR-NCX-SERCA local cross-talk ensures pacemaker cell function at rest and during the fight-or-flight reflex. Circ Res 113:e94-e100
Stern, Michael D (2012) Coagulation makes waves. Biophys J 103:2049
Zahanich, Ihor; Sirenko, Syevda G; Maltseva, Larissa A et al. (2011) Rhythmic beating of stem cell-derived cardiac cells requires dynamic coupling of electrophysiology and Ca cycling. J Mol Cell Cardiol 50:66-76
Yaniv, Yael; Maltsev, Victor A; Escobar, Ariel L et al. (2011) Beat-to-beat Ca(2+)-dependent regulation of sinoatrial nodal pacemaker cell rate and rhythm. J Mol Cell Cardiol 51:902-5
Maltsev, Victor A; Vinogradova, Tatiana M; Stern, Michael D et al. (2011) Letter to the editor: ""Validating the requirement for beat-to-beat coupling of the Ca2+ clock and M clock in pacemaker cell normal automaticity"". Am J Physiol Heart Circ Physiol 300:H2323-4; author reply H2325-6
Maltsev, Anna V; Maltsev, Victor A; Mikheev, Maxim et al. (2011) Synchronization of stochastic Ca²(+) release units creates a rhythmic Ca²(+) clock in cardiac pacemaker cells. Biophys J 100:271-83

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