Affiliation:
1. Laboratory of Heart Electrophysiology Cardiology Research Centre Moscow Russian Federation
2. Department of Medicine Cardiovascular Medicine University of Wisconsin‐Madison School of Medicine and Public Health Madison WI
3. Department of Pediatrics Pediatric Cardiology University of Wisconsin‐Madison School of Medicine and Public Health Madison WI
Abstract
Background
Atrial fibrillation often occurs in the setting of hypertension and associated atrial dilation with pathologically increased cardiomyocyte stretch. In the setting of atrial dilation, mechanoelectric feedback has been linked to the development of ectopic beats that trigger paroxysmal atrial fibrillation mainly originating from pulmonary veins (
PVs
). However, the precise mechanisms remain poorly understood.
Methods and Results
We identify mechanosensitive, swelling‐activated chloride ion channels (
I
C
l,swell
) as a crucial component of the caveolar mechanosensitive complex in rat and human cardiomyocytes. In vitro optical mapping of rat
PV
, single rat
PV
, and human cardiomyocyte patch clamp studies showed that stretch‐induced activation of
I
Cl,swell
leads to membrane depolarization and decreased action potential amplitude, which trigger conduction discontinuities and both ectopic and reentrant activities within the
PV
. Reverse transcription quantitative polymerase chain reaction, immunofluorescence, and coimmunoprecipitation studies showed that
I
Cl,swell
likely consists of at least 2 components produced by mechanosensitive ClC‐3 (chloride channel‐3) and
SWELL
1 (also known as LRRC8A [leucine rich repeat containing protein 8A]) chloride channels, which form a macromolecular complex with caveolar scaffolding protein Cav3 (caveolin 3). Downregulation of Cav3 protein expression and disruption of caveolae structures during chronic hypertension in spontaneously hypertensive rats facilitates activation of
I
Cl,swell
and increases
PV
sensitivity to stretch 10‐ to 50‐fold, promoting the development of atrial fibrillation.
Conclusions
Our findings identify caveolae‐mediated activation of mechanosensitive
I
Cl,swell
as a critical cause of
PV
ectopic beats that can initiate atrial arrhythmias including atrial fibrillation. This mechanism is exacerbated in the setting of chronically elevated blood pressures.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine
Cited by
30 articles.
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