An integrative model of the cardiac ventricular myocyte incorporating local control of Ca2+ release

Joseph L. Greenstein, Raimond L. Winslow

Research output: Contribution to journalArticle

Abstract

The local control theory of excitation-contraction (EC) coupling in cardiac muscle asserts that L-type Ca2+ current tightly controls Ca2+ release from the sarcoplasmic reticulum (SR) via local interaction of closely apposed L-type Ca2+ channels (LCCs) and ryanodine receptors (RyRs). These local interactions give rise to smoothly graded Ca2+-induced Ca2+ release (CICR), which exhibits high gain. In this study we present a biophysically detailed model of the normal canine ventricular myocyte that conforms to local control theory. The model formulation incorporates details of microscopic EC coupling properties in the form of Ca2+ release units (CaRUs) in which individual sarcolemmal LCCs interact in a stochastic manner with nearby RyRs in localized regions where junctional SR membrane and transverse-tubular membrane are in close proximity. The CaRUs are embedded within and interact with the global systems of the myocyte describing ionic and membrane pump/exchanger currents, SR Ca2+ uptake, and time-varying cytosolic ion concentrations to form a model of the cardiac action potential (AP). The model can reproduce both the detailed properties of EC coupling, such as variable gain and graded SR Ca2+ release, and whole-cell phenomena, such as modulation of AP duration by SR Ca2+ release. Simulations indicate that the local control paradigm predicts stable APs when the L-type Ca2+ current is adjusted in accord with the balance between voltage- and Ca2+-dependent inactivation processes as measured experimentally, a scenario where common pool models become unstable. The local control myocyte model provides a means for studying the interrelationship between microscopic and macroscopic behaviors in a manner that would not be possible in experiments.

Original languageEnglish (US)
Pages (from-to)2918-2945
Number of pages28
JournalBiophysical journal
Volume83
Issue number6
DOIs
StatePublished - Dec 1 2002

ASJC Scopus subject areas

  • Biophysics

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