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Updated: Jul 19, 2026

Isolation of Atrial Myocytes from Adult Mice
Published on: July 25, 2019
Extended atrial conduction system characterised by the expression of the HCN4 channel and connexin45
Mitsuru Yamamoto1, Halina Dobrzynski, James Tellez
1Research Institute of Environmental Medicine, Nagoya University, Nagoya 464-8601, Japan.
Insights
The hyperpolarization-activated cyclic nucleotide-gated channel 4 (HCN4) is widely distributed in the atria, explaining pacemaker site variations and ectopic foci in atrial tachycardia.
Area of Science:
- Cardiovascular Physiology
- Cardiac Electrophysiology
- Molecular Cardiology
Background:
- The heart utilizes multiple supraventricular pacemakers for normal rhythm and arrhythmias.
- HCN4 is the primary isoform responsible for the pacemaker current, I(f).
Purpose of the Study:
- To investigate the distribution of HCN4 within the atria.
- To correlate HCN4 distribution with pacemaker activity and potential arrhythmia origins.
Main Methods:
- Immunohistochemistry was used to localize HCN4 and connexins in rat atria.
- Extracellular electrodes recorded electrical activity to identify pacemaker sites.
Main Results:
- HCN4 and connexin 45 (Cx45) were found in the sinoatrial node and a novel nodal-like tract.
- This HCN4-expressing tract demonstrated pacemaking capability, suggesting a pacemaker hierarchy.
- HCN4 was also present in the atrioventricular ring around the tricuspid valve but not the mitral valve or pulmonary veins.
Conclusions:
- The extensive distribution of HCN4 in the atria explains the variable location of the leading pacemaker site.
- Widespread HCN4 expression accounts for the broad area requiring ablation to control sinus rhythm.
- It also clarifies the origin of ectopic foci causing atrial tachycardia.
Objective:
In the heart, there are multiple supraventricular pacemakers involved in normal pacemaking as well as arrhythmias and the objective was to determine the distribution of HCN4 (major isoform underlying the pacemaker current, I(f)) in the atria.
Methods:
In the atria of the rat, the localisation of HCN4 and connexins was determined using immunohistochemistry, and electrical activity was recorded using extracellular electrodes.
Results:
As expected, HCN4 and Cx45 (but not Cx43) were expressed in the sinoatrial node extending from the superior vena cava down the crista terminalis. The same pattern of expression of HCN4 and connexins was observed in a novel tract of nodal-like cells extending from the superior vena cava down the interatrial groove. Although the sinoatrial node was usually the leading pacemaker site, the novel tract of HCN4-expressing cells was capable of pacemaking and could act as the leading pacemaker site; there was evidence of a hierarchy of pacemakers. The same pattern of expression of HCN4 and connexins was also observed in the atrioventricular ring bundle (including the atrioventricular node) encircling the tricuspid valve, but not in the atrioventricular ring bundle encircling the mitral valve. HCN4 was not expressed in the pulmonary veins.
Conclusions:
The widespread distribution of HCN4 can explain the widespread location of the leading pacemaker site during sinus rhythm, the extensive region of tissue that has to be ablated to stop sinus rhythm, and the widespread distribution of ectopic foci responsible for atrial tachycardia.
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