The Emergence of a General Theory of the Initiation and Strength of the Heartbeat

Abstract

Sarcoplasmic reticulum (SR) Ca²⁺ cycling, that is, the Ca²⁺ clock, entrained by externally delivered action potentials has been a major focus in ventricular myocyte research for the past 5 decades. In contrast, the focus of pacemaker cell research has largely been limited to membrane-delimited pacemaker mechanisms (membrane clock) driven by ion channels, as the immediate cause for excitation. Recent robust experimental evidence, based on confocal cell imaging, and supported by numerical modeling suggests a novel concept: the normal rhythmic heart beat is governed by the tight integration of both intracellular Ca²⁺ and membrane clocks. In pacemaker cells the intracellular Ca²⁺ clock is manifested by spontaneous, rhythmic submembrane local Ca²⁺ releases from SR, which are tightly controlled by a high degree of basal and reserve PKA-dependent protein phosphorylation. The Ca²⁺ releases rhythmically activate Na⁺/Ca²⁺ exchange inward currents that ignite action potentials, whose shape and ion fluxes are tuned by the membrane clock which, in turn, sustains operation of the intracellular Ca²⁺ clock. The idea that spontaneous SR Ca²⁺ releases initiate and regulate normal automaticity provides the key that reunites pacemaker and ventricular cell research, thus evolving a general theory of the initiation and strength of the heartbeat.