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Originally published as Biophys J. BioFAST on May 16, 2008.
doi:10.1529/biophysj.107.125948
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Biophysical Journal 95:1689-1703 (2008)
© 2008 The Biophysical Society

Moment Closure for Local Control Models of Calcium-Induced Calcium Release in Cardiac Myocytes

George S. B. Williams *, Marco A. Huertas *, Eric A. Sobie {dagger}, M. Saleet Jafri {ddagger} and Gregory D. Smith * §

* Department of Applied Science, College of William and Mary, Williamsburg, Virginia; {dagger} Department of Bioinformatics and Computational Biology, George Mason University, Manassas, Virginia; {ddagger} Department of Pharmacology and Systems Therapeutics, Mount Sinai School of Medicine, New York, New York; and § Mathematical Biosciences Institute, The Ohio State University, Columbus, Ohio

Correspondence: Address reprint requests to Gregory D. Smith, E-mail: greg{at}as.wm.edu.

In prior work, we introduced a probability density approach to modeling local control of Ca2+-induced Ca2+ release in cardiac myocytes, where we derived coupled advection-reaction equations for the time-dependent bivariate probability density of subsarcolemmal subspace and junctional sarcoplasmic reticulum (SR) [Ca2+] conditioned on Ca2+ release unit (CaRU) state. When coupled to ordinary differential equations (ODEs) for the bulk myoplasmic and network SR [Ca2+], a realistic but minimal model of cardiac excitation-contraction coupling was produced that avoids the computationally demanding task of resolving spatial aspects of global Ca2+ signaling, while accurately representing heterogeneous local Ca2+ signals in a population of diadic subspaces and junctional SR depletion domains. Here we introduce a computationally efficient method for simulating such whole cell models when the dynamics of subspace [Ca2+] are much faster than those of junctional SR [Ca2+]. The method begins with the derivation of a system of ODEs describing the time-evolution of the moments of the univariate probability density functions for junctional SR [Ca2+] jointly distributed with CaRU state. This open system of ODEs is then closed using an algebraic relationship that expresses the third moment of junctional SR [Ca2+] in terms of the first and second moments. In simulated voltage-clamp protocols using 12-state CaRUs that respond to the dynamics of both subspace and junctional SR [Ca2+], this moment-closure approach to simulating local control of excitation-contraction coupling produces high-gain Ca2+ release that is graded with changes in membrane potential, a phenomenon not exhibited by common pool models. Benchmark simulations indicate that the moment-closure approach is nearly 10,000-times more computationally efficient than corresponding Monte Carlo simulations while leading to nearly identical results. We conclude by applying the moment-closure approach to study the restitution of Ca2+-induced Ca2+ release during simulated two-pulse voltage-clamp protocols.







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Copyright © 2008 by the Biophysical Society.