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Updated: Mar 5, 2026

Isolation of Human Atrial Myocytes for Simultaneous Measurements of Ca2+ Transients and Membrane Currents
Published on: July 3, 2013
Calcium signalling silencing in atrial fibrillation
1Center for Biomedical Engineering and Technology and Department of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Insights
Subcellular calcium signalling silencing is an adaptive response to rapid heart activation during atrial fibrillation (AF). This mechanism reduces calcium instability and arrhythmogenicity, offering a protective effect against AF progression.
Area of Science:
- Cardiology
- Cellular Biology
- Molecular Biology
Background:
- Rapid cardiac activation, as seen in paroxysmal atrial fibrillation (AF), triggers cellular responses.
- Intracellular calcium (Ca2+) signalling instability contributes to arrhythmogenicity in AF.
- Understanding adaptive responses is crucial for managing AF.
Purpose of the Study:
- To investigate subcellular calcium signalling silencing as a novel adaptive response to rapid cardiac activation in AF.
- To elucidate the molecular mechanisms and functional consequences of calcium signalling silencing in AF.
Main Methods:
- Analysis of subcellular calcium signalling in patients with AF and a rabbit model.
- Assessment of calcium release channel (ryanodine receptor, RyR2) expression levels.
- Measurement of Ca2+ sparks, arrhythmogenic Ca2+ waves, action potentials, and L-type Ca2+ current.
Main Results:
- Calcium signalling silencing was observed in patients with AF and a rabbit model, characterized by failed Ca2+ signal propagation.
- This adaptive response significantly reduced ryanodine receptor (RyR2) expression and the frequency of Ca2+ sparks and waves.
- Key features include reduced Ca2+ release, enhanced Ca2+ buffering, shortened action potentials, and decreased intracellular Na+.
Conclusions:
- Calcium signalling silencing is a distinct anti-arrhythmic adaptive mechanism counteracting Ca2+-based arrhythmogenicity in AF.
- This process limits the pro-arrhythmic role of unstable Ca2+ signalling during AF.
- The AF Ca2+ signalling phenotype results from a balance between stabilizing (silencing) and destabilizing factors.
Abstract:
Subcellular calcium signalling silencing is a novel and distinct cellular and molecular adaptive response to rapid cardiac activation. Calcium signalling silencing develops during short-term sustained rapid atrial activation as seen clinically during paroxysmal atrial fibrillation (AF). It is the first 'anti-arrhythmic' adaptive response in the setting of AF and appears to counteract the maladaptive changes that lead to intracellular Ca2+ signalling instability and Ca2+ -based arrhythmogenicity. Calcium signalling silencing results in a failed propagation of the [Ca2+ ]i signal to the myocyte centre both in patients with AF and in a rabbit model. This adaptive mechanism leads to a substantial reduction in the expression levels of calcium release channels (ryanodine receptors, RyR2) in the sarcoplasmic reticulum, and the frequency of Ca2+ sparks and arrhythmogenic Ca2+ waves remains low. Less Ca2+ release per [Ca2+ ]i transient, increased fast Ca2+ buffering strength, shortened action potentials and reduced L-type Ca2+ current contribute to a substantial reduction of intracellular [Na+ ]. These features of Ca2+ signalling silencing are distinct and in contrast to the changes attributed to Ca2+ -based arrhythmogenicity. Some features of Ca2+ signalling silencing prevail in human AF suggesting that the Ca2+ signalling 'phenotype' in AF is a sum of Ca2+ stabilizing (Ca2+ signalling silencing) and Ca2+ destabilizing (arrhythmogenic unstable Ca2+ signalling) factors. Calcium signalling silencing is a part of the mechanisms that contribute to the natural progression of AF and may limit the role of Ca2+ -based arrhythmogenicity after the onset of AF.
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