Skip to main content


Front. Physiol., 09 October 2018
Sec. Cardiac Electrophysiology
Volume 9 - 2018 |

Profibrotic, Electrical, and Calcium-Handling Remodeling of the Atria in Heart Failure Patients With and Without Atrial Fibrillation

Cristina E. Molina1,2,3† Issam H. Abu-Taha1† Qiongling Wang4 Elena Roselló-Díez5 Marcus Kamler6 Stanley Nattel1,7,8 Ursula Ravens9,10 Xander H. T. Wehrens4 Leif Hove-Madsen2 Jordi Heijman11 Dobromir Dobrev1*
  • 1Institute of Pharmacology, West German Heart and Vascular Center, University Duisburg-Essen, Essen, Germany
  • 2Biomedical Research Institute Barcelona (IIBB-CSIC) and Biomedical Research Institute Sant Pau, Hospital de Sant Pau, Barcelona, Spain
  • 3Institute of Experimental Cardiovascular Research, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
  • 4Cardiovascular Research Institute – Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, TX, United States
  • 5Cardiac Surgery Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
  • 6Department of Thoracic and Cardiovascular Surgery, West German Heart and Vascular Center Essen, University Hospital Essen, Essen, Germany
  • 7Department of Medicine, Montreal Heart Institute and Université de Montréal, Montreal, QC, Canada
  • 8Department of Pharmacology and Therapeutics, McGill University, Montreal, QC, Canada
  • 9Institute of Experimental Cardiovascular Medicine, University Heart Center Freiburg, University of Freiburg, Bad Krozingen, Germany
  • 10Institute of Physiology, Medical Faculty Carl Gustav Carus, TU Dresden, Dresden, Germany
  • 11Department of Cardiology, CARIM School for Cardiovascular Diseases, Maastricht University, Maastricht, Netherlands

Atrial fibrillation (AF) and heart failure (HF) are common cardiovascular diseases that often co-exist. Animal models have suggested complex AF-promoting atrial structural, electrical, and Ca2+-handling remodeling in the setting of HF, but data in human samples are scarce, particularly regarding Ca2+-handling remodeling. Here, we evaluated atrial remodeling in patients with severe left ventricular (LV) dysfunction (HFrEF), long-standing persistent (‘chronic’) AF (cAF) or both (HFrEF-cAF), and sinus rhythm controls with normal LV function (Ctl) using western blot in right-atrial tissue, sharp-electrode action potential (AP) measurements in atrial trabeculae and voltage-clamp experiments in isolated right-atrial cardiomyocytes. Compared to Ctl, expression of profibrotic markers (collagen-1a, fibronectin, periostin) was higher in HFrEF and HFrEF-cAF patients, indicative of structural remodeling. Connexin-43 expression was reduced in HFrEF patients, but not HFrEF-cAF patients. AP characteristics were unchanged in HFrEF, but showed classical indices of electrical remodeling in cAF and HFrEF-cAF (prolonged AP duration at 20% and shorter AP duration at 50% and 90% repolarization). L-type Ca2+ current (ICa,L) was significantly reduced in HFrEF, cAF and HFrEF-cAF, without changes in voltage-dependence. Potentially proarrhythmic spontaneous transient-inward currents were significantly more frequent in HFrEF and HFrEF-cAF compared to Ctl, likely resulting from increased sarcoplasmic reticulum (SR) Ca2+ load (integrated caffeine-induced current) in HFrEF and increased ryanodine-receptor (RyR2) single-channel open probability in HFrEF and HFrEF-cAF. Although expression and phosphorylation of the SR Ca2+-ATPase type-2a (SERCA2a) regulator phospholamban were unchanged in HFrEF and HFrEF-cAF patients, protein levels of SERCA2a were increased in HFrEF-cAF and sarcolipin expression was decreased in both HFrEF and HFrEF-cAF, likely increasing SR Ca2+ uptake and load. RyR2 protein levels were decreased in HFrEF and HFrEF-cAF patients, but junctin levels were higher in HFrEF and relative Ser2814-RyR2 phosphorylation levels were increased in HFrEF-cAF, both potentially contributing to the greater RyR2 open probability. These novel insights into the molecular substrate for atrial arrhythmias in HF-patients position Ca2+-handling abnormalities as a likely trigger of AF in HF patients, which subsequently produces electrical remodeling that promotes the maintenance of the arrhythmia. Our new findings may have important implications for the development of novel treatment options for AF in the context of HF.


Atrial fibrillation (AF) and heart failure (HF) are common cardiovascular diseases, negatively affecting morbidity and mortality of millions of patients worldwide (Benjamin et al., 2018). AF and HF frequently co-exist, and HF is a strong independent risk factor for the development of AF (Ling et al., 2016; Sartipy et al., 2017). AF prevalence increases with the severity of HF, ranging from 5% in NYHA Class I to 40–50% in NYHA Class IV (Andrade et al., 2014). The presence of AF in HF patients is associated with a worse prognosis (Wang et al., 2003; Mogensen et al., 2017). In agreement, the CASTLE-AF study has recently demonstrated that maintenance of sinus rhythm in HF patients with reduced left ventricular (LV) ejection fraction (HFrEF) through catheter ablation of AF significantly reduces mortality (Marrouche et al., 2018).

The common clinical coincidence of AF and HF may in part be due to their shared dependence on risk factors such as hypertension and diabetes. In addition, several bidirectional mechanistic interactions between AF and HF may promote the co-existence of both diseases in patients (Heijman et al., 2013; Hohendanner et al., 2018). For example, the atrial contribution to cardiac output is lost in the setting of AF and AF may promote ventricular dysfunction when ventricular rate is not well controlled. On the other hand, HF chronically elevates atrial pressure and causes atrial stretch, while activating systemic neurohumoral signaling pathways that affect the atria. Both components are expected to produce AF-promoting atrial remodeling. Indeed, AF is increasingly regarded as a symptom of an atrial cardiomyopathy produced by a wide variety of pathophysiological processes (Goette et al., 2017), which might be the first clinical sign of compromised ventricular function.

Animal models have identified complex atrial electrical remodeling in HF, which differs depending on species, as well as type (myocardial infarction vs. ventricular tachypacing) and duration of HF (Pandit and Workman, 2016). By contrast, structural remodeling, including activation of profibrotic signaling pathways, is a consistent finding in most HF models (Li et al., 1999; Cardin et al., 2003; Milliez et al., 2005; Yamada et al., 2017). Finally, accumulating evidence also suggests an important role for Ca2+-handling abnormalities in the increased susceptibility to AF in various HF models (Yeh et al., 2008; Lugenbiel et al., 2015; Pluteanu et al., 2018).

Multiple components of atrial remodeling in patients have been characterized for different forms of AF (Brundel et al., 2002; Schotten et al., 2011; Jalife and Kaur, 2015; Simon et al., 2016). Electrical remodeling (notably shortening of action potential [AP] duration [APD]) (Dobrev et al., 2001; Voigt et al., 2012; Schmidt et al., 2015) and structural remodeling (hypertrophy and increased fibrosis) are consistent findings in patients with long-standing persistent (‘chronic’) AF (cAF) (Polyakova et al., 2008; Cao et al., 2010). Ca2+-handling abnormalities have been identified in both paroxysmal AF and cAF, although the underlying molecular mechanisms are distinct (Voigt et al., 2012, 2014; Beavers et al., 2013). However, information about AF-promoting atrial remodeling in HFrEF patients is limited and inconsistent (Ling et al., 2016; Pandit and Workman, 2016), with reduced, unchanged or prolonged cardiomyocyte APD being reported in HFrEF patients (Schreieck et al., 2000; Workman et al., 2009; Schmidt et al., 2017). On electroanatomical mapping, APDs are rather prolonged in HF patients (Sanders et al., 2003), paralleling findings in animal models (Li et al., 2000). Similar to animal models, atrial structural remodeling, including fibrosis, is commonly observed in HF patients (Xu et al., 2004; Akkaya et al., 2013). However, whether HF is associated with atrial Ca2+-handling abnormalities in humans and whether the underlying mechanisms are similar to those observed in patients with AF is not known. Moreover, patients with HF-dependent AF are subjected to both HF- and AF-related remodeling. Due to the cross-talk between both processes, the resulting remodeling is likely different from and more complex than the sum of the individual processes (Cha et al., 2004; Heijman et al., 2013; Goette et al., 2017), but has not yet been characterized in atrial samples from patients.

Here, we assessed for the first time atrial profibrotic, electrical and Ca2+-handling remodeling in atrial samples from patients with HFrEF and HFrEF-cAF to sinus-rhythm patients with normal LV ejection fraction (Ctl). We obtained evidence for substantial profibrotic and Ca2+-handling remodeling in HFrEF patients, but did not find indices of classical electrical remodeling. Proarrhythmic diastolic Ca2+-release events and profibrotic remodeling were similarly observed in HFrEF-cAF patients, along with classical AF-related electrical remodeling, consistent with the more complex pathophysiology present in these patients. Overall, our new data position Ca2+-handling abnormalities as a potential early component of HF-related atrial remodeling, which in fibrotic atria may initiate AF episodes that induce electrical remodeling, promoting arrhythmia-stabilizing reentry and AF persistence.

Materials and Methods

Human Tissue Samples

Right-atrial (RA) appendages were obtained from 79 Ctl patients (LV ejection fraction > 50%), 40 patients with HFrEF, 35 patients with cAF and 36 HFrEF-cAF undergoing open-heart surgery. Mean LV ejection fraction was <35% for HFrEF and HFrEF-cAF. Patient characteristics are provided in Tables 13. Experimental protocols were approved by ethical review boards of Dresden University of Technology, Hospital de la Santa Creu i Sant Pau and University Hospital Essen, and were conducted in accordance with the Declaration of Helsinki. Each patient gave written informed consent. The tissue samples were collected just prior to atrial cannulation for extracorporeal circulatory bypass, stored in Tyrode solution and transferred to the laboratory for AP recordings in trabeculae, cardiomyocyte isolation for voltage-clamp studies, or freezing in liquid nitrogen for biochemical and biophysical experiments, as detailed below.


TABLE 1. Clinical characteristics of patient samples employed for multicellular action potential recordings.


TABLE 2. Clinical characteristics of patient samples used for voltage-clamp recordings in isolated atrial cardiomyocytes.


TABLE 3. Clinical characteristics of patient samples employed for biochemical experiments.

Western Blot Analysis

Western blot analyses were performed as previously described (El-Armouche et al., 2006; Shanmugam et al., 2011). In brief, atrial lysates were subjected to electrophoresis on 5% or 10% acrylamide gels, or 10% Bis-Tris gels (Thermo Fisher Scientific, Waltham, MA, United States) for analyses of sarcolipin, followed by transfer onto polyvinyl difluoride (PVDF) or nitrocellulose membranes. Protein levels of α smooth-muscle actin (αSMA, 1:500, A5228, Sigma-Aldrich, St. Louis, MO, United States), calsequestrin (CSQ, 1:2,500, PA1-913, Thermo Fisher Scientific), collagen 1α (Col1a, 1:1,000, sc-293182, Santa Cruz Biotechnology, Santa Cruz, CA, United States), connexin-40 (Cx40, 1:1,000, ab1726, Merck Millipore, Burlington, MA, United States), total and Ser368-phosphorylated connexin-43 (Cx43, 1:1,000, 3511, Cell Signaling Technology, Danvers, MA, United States), fibronectin (1:1,000, sc-8422, Santa Cruz Biotechnology), GAPDH (1:20,000, 5G4 6C5, HyTest, Turku, Finland), junctin (1:2,000, LS-C196703, LifeSpan BioSciences, Seattle, WA, United States), junctophilin-2 (1:1,000, sc-134875, Santa Cruz), matrix metallopeptidase 9 (MMP9, 1:200, ab38898, Abcam, Cambridge, United Kingdom), Na+-Ca2+-exchanger type-1 (NCX1, 1:1,000, R3F1, Swant, Marly, Switzerland), periostin (1:1,000, sc-134875, Santa Cruz Biotechnology), total, Ser16- and Thr17-phosphorylated phospholamban (PLB, all 1:1,000, ab2865 and ab92697, Abcam, Cambridge, United Kingdom and A010-13, Badrilla Ltd., Leeds, United Kingdom), total ryanodine receptor type-2 channel (RyR2, 1:1,000, MA3-916, Thermo Fisher Scientific), sarcolipin (1:100, ABT13, Merck Millipore), sarcoplasmic reticulum (SR) Ca2+-ATPase type-2a (SERCA2a; 1:2,000, sc-8095, Santa Cruz Biotechnology), transforming growth factor β1 (TGF-β1, 1:1000, ab9758, Abcam), and vimentin (1:1,000, sc373717, Santa Cruz Biotechnology) were determined using appropriate primary antibodies. The Ser2808-RyR2 and Ser2814-RyR2 phospho-epitope-specific antibodies (both 1:2,000) were custom generated, as previously described (Voigt et al., 2012). Appropriate near-infrared fluorophore dyes (IRDye, all 1:20,000, LI-COR Biosciences, Lincoln, NE, United States) were employed as secondary antibodies and imaged with an Odyssey Infrared Imaging System (LI-COR Biosciences). Protein expression was normalized to GAPDH.

Electrophysiological Recordings

Action potentials were recorded in trabeculae isolated from RA appendages using the standard microelectrode technique as previously described, with microelectrode tip resistance of 10–25 MΩ and 1 ms stimulus, 25% above threshold intensity applied at a frequency of 1 Hz (Wettwer et al., 2004; Loose et al., 2014). The bath solution contained (in mmol/L): NaCl 127, KCl 4.5, MgCl2 1.5, CaCl2 1.8, glucose 10, NaHCO3 22, and NaH2PO4 0.42, equilibrated with O2/CO2 (95:5) at 35 ± 2°C and pH = 7.4.

Cardiomyocyte isolation was performed according to previously established protocols (Llach et al., 2011; Molina et al., 2012; Voigt et al., 2015). Briefly, enzymatic digestion was carried out in a Ca2+-free Tyrode solution containing 0.5 mg/ml collagenase (Worthington type 2, 300 u/mg), 0.25 mg/ml proteinase (Sigma type XXIV, 11 u/mg solid) and 5% bovine fatty acid-free albumin. After 30 min at 37°C, the tissue was removed from the enzyme solution, and cells were disaggregated in Ca2+-free solution. The remaining tissue was digested for 3 × 15 min in a fresh Ca2+-free solution containing 0.4 mg/ml collagenase. Only elongated cells with clear cross striations and without granulation were used for experiments. Total membrane currents were measured at room temperature in the perforated-patch configuration with an EPC-10 amplifier (HEKA Elektronik, Germany), as previously described (Llach et al., 2011; Molina et al., 2012). The extracellular solution contained (in mmol/L): NaCl 127, TEA 5, HEPES 10, NaHCO3 4, NaH2PO4 0.33, glucose 10, pyruvic acid 5, CaCl2 2, MgCl2 1.8 (pH = 7.4) and the pipette solution contained (in mmol/L): aspartic acid 109, CsCl 47, Mg2ATP 3, MgCl2 1, Na2-phosphocreatine 5, Li2GTP 0.42, HEPES 10 (pH = 7.2 with CsOH). Amphotericin B (250 μg/ml) was added to the pipette solution before starting the experiment. All chemicals were acquired from Sigma-Aldrich.

The L-type calcium current (ICa,L) was measured using a 50 ms prepulse from -80 to -45 mV to inactivate the fast Na+ current, followed by a 200 ms depolarization to +10 mV and ICa,L amplitude was determined as the difference between the peak inward current and the current at the end of the depolarization (Llach et al., 2011; Molina et al., 2012). The current–voltage relationship for ICa,L and the voltage-dependent inactivation were obtained using test potentials between -40 and +50 mV. The time constants of ICa,L inactivation were determined from a bi-exponential fit of the decaying phase of ICa,L. Recovery of ICa,L from inactivation was assessed using a two-pulse protocol with increasing intervals between the first and the second pulse used to elicit ICa,L.

The SR Ca2+ content was measured at room temperature as the time integral of the current elicited by rapid exposure to 10 mmol/L caffeine to release all Ca2+ from the SR, activating NCX1, and was converted to amoles (10-18 mol) of calcium released from the SR, assuming a stoichiometry of 3 Na+ to 1 Ca2+ for NCX1. Spontaneous calcium releases were examined as transient-inward currents (INCX) with the membrane potential clamped at -80 mV, as previously described (Hove-Madsen et al., 2004; Llach et al., 2011; Molina et al., 2012; Voigt et al., 2012).

RyR2 Single-Channel Recordings

RyR2 single-channel recordings were obtained as previously described (Wehrens et al., 2003). In brief, SR membrane-preparations were incorporated into lipid-bilayer membranes made of a 3:1 mixture of phosphatidylethanolamine and phosphatidylserine (Avanti Polar Lipids, Alabaster, AL, United States) dissolved in n-decane (25 mg/ml). Bilayers were formed across a 150 μm aperture of a polystyrene cuvette. The trans chamber (luminal side of the SR) contained (in mmol/L): HEPES 250, KCl 50 and Ca(OH)2 53. The cis chamber (cytosolic side of the SR) contained (in mmol/L): HEPES 250, Tris-base 125, KCl 50, EGTA 1, CaCl2 0.5 (pH = 7.35). At the end of each experiment, ryanodine (5 μmol/L) was applied to the cis chamber to confirm identity of RyR2 channels. Data were collected using Digidata 1322A (Molecular Devices, Sunnyvale, CA, United States) and Warner Bilayer Clamp Amplifier BC-535 (Warner Instruments, Hamden, CT, United States) at 0 mV under voltage-clamp conditions. Cytosolic free Ca2+ was calculated with WinMax32. Data were analyzed from digitized current recordings using pCLAMP-9.2 software (Molecular Devices).

Data Analysis and Statistics

Data are presented as mean ± standard error (SEM) or scatter plots of individual measurements with 95% confidence interval and interquartile ranges. Normality was assessed using D’Agostino and Pearson omnibus test. For multicellular AP recordings, biochemical experiments, and clinical parameters, for which each patient contributed a single data point, one-way ANOVA followed by a post hoc Bonferroni t-test was used to compare means between groups for normally distributed continuous data. Continuous data which did not follow a normal distribution or for which normality could not be assessed were compared using a Kruskal–Wallis test with Dunn’s multiple comparison t-test. Categorical data were analyzed using a Chi-squared test with Bonferroni correction for multiple comparisons when comparing more than two groups. For patch-clamp and RyR2 single-channel recordings, in which each patient may contribute multiple data points, hierarchical statistics were employed according to recently published methods (Sikkel et al., 2017). Logarithmic transformations were applied to non-normal-distributed data (RyR2 properties and frequency of spontaneous SR Ca2+-release events) before applying hierarchical statistical analyses. P < 0.05 was considered statistically significant.


Patient Characteristics

Major clinical parameters for all patient groups are provided in Table 1 (for patient samples employed for multicellular AP recordings), Table 2 (for patient samples used for cardiomyocyte isolation and voltage-clamp experiments), and Table 3 (for patient samples used for biochemical experiments). By definition, LV ejection fractions were significantly lower in HFrEF and HFrEF-cAF groups compared to Ctl and cAF. In addition, there was a strong trend toward increased left atrial diameter in HFrEF patients, which was even more pronounced in cAF and HFrEF-cAF patients. As expected, HFrEF patients also tended to take more β-blockers, whereas AF patients more often received digitalis. There were no other major differences in clinical parameters between the three groups.

Profibrotic Remodeling

Patients with HFrEF have increased macroscopic fibrosis and conduction slowing (Sanders et al., 2003; Akkaya et al., 2013). Moreover, animal models of HF consistently show increased molecular markers of profibrotic remodeling (Cardin et al., 2003). We evaluated protein expression levels of key extracellular matrix components (col1a, fibronectin, MMP9), activated fibroblast/(myo)fibroblast markers (vimentin, periostin, αSMA) and profibrotic signaling molecules (TGF-β1) in atrial tissue homogenates of Ctl, HFrEF and HFrEF-cAF patients (Figure 1A). Compared to Ctl patients, col1a, fibronectin and periostin were significantly increased in HFrEF and HFrEF-cAF patients, consistent with increased fibrosis in these patients.


FIGURE 1. Atrial profibrotic and connexin remodeling. (A) Representative Western blot examples (top) and quantification of protein expression (bottom; mean ± SEM) of periostin, vimentin, α-smooth muscle actin (α-SMA), matrix metallopeptidase 9 (MMP9), transforming growth factor-β1 (TGF-β1), fibronectin and collagen 1α (col1a) in right-atrial tissue homogenates from Ctl (white bars), HFrEF (blue bars) or HFrEF-cAF (red/blue-striped bars) patients. Vertical white lines separate non-adjacent lanes on the same blot. (B) Representative Western blot examples (top) and quantification of protein expression (bottom; mean ± SEM) of total connexin-40 (Cx40), total and Ser368-phosphorylated connexin-43 (Cx43). GAPDH was used as loading control and is shown for the samples used for Western blots of periostin, vimentin, α-SMA and MMP9, for TGF-β1, and for fibronectin and col1a. Numbers in bars indicate number of patients. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF.

Electrical Remodeling

First we assessed the protein expression of connexin isoforms contributing to electrical cell-to-cell coupling and signaling. Protein levels of Cx40 were not different between the three groups, whereas protein expression of total Cx43 was reduced by ∼41% (P = 0.078) in atrial homogenates of HFrEF patients, but was not different between Ctl and HFrEF-cAF patients (Figure 1B). Similarly, steady-state phosphorylation levels of Cx43 at Ser368, which control internalization of connexins (Cone et al., 2014), were reduced by ∼36% in HFrEF only (Figure 1B), potentially contributing to the conduction slowing observed in vivo (Sanders et al., 2003).

Next, we recorded APs in multicellular preparations from Ctl, HFrEF, cAF and HFrEF-cAF patients (Figure 2A). There were no significant differences in resting membrane potential, upstroke velocity (maximum dV/dt), conduction time, plateau potential or APD at 20%, 50%, or 90% of repolarization between Ctl and HFrEF patients (Figure 2B). By contrast, patients with cAF or HFrEF-cAF had a significantly increased plateau potential, significantly prolonged APD at 20% repolarization, and significantly shorter APD at 50% and 90% repolarization compared to Ctl (P < 0.01 for all; Figure 2B). There was a trend toward an increased AP amplitude in HFrEF (P = 0.077 vs. Ctl), which was significant in patients with cAF or HFrEF-cAF.


FIGURE 2. Electrical remodeling in multicellular human atrial trabeculae. (A) Representative action potential (AP) recordings in multicellular preparations from Ctl, HFrEF, cAF or HFrEF-cAF patients (from left to right). (B) Quantification of AP parameters in Ctl (white bars), HFrEF (blue bars), cAF (red bars) or HFrEF-cAF (red/blue-striped bars) patients. Top row shows (from left to right): resting membrane potential (RMP), AP amplitude (APA), maximal AP upstroke velocity (dV/dtmax) and conduction time (note different n-numbers). Bottom row shows (from left to right): level of AP plateau and AP duration (APD) at 20%, 50%, and 90% of repolarization. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF. Numbers indicate number of patients.

Then, we investigated ICa,L properties in isolated human atrial cardiomyocytes as a potential contributor to electrical remodeling and marker of Ca2+-handling remodeling. HFrEF, cAF and HFrEF-cAF patients all had a significant decrease in peak ICa,L amplitude (Figure 3A). Voltage-dependence of peak ICa,L (Figure 3B), inactivation (Figures 3C,D), and the time constant of recovery from inactivation (Figure 3F) were not different between Ctl, HFrEF, cAF and HFrEF-cAF patients. We determined the fast and slow time constants of ICa,L inactivation through a biexponential fit. Although the fast time constant was not different between Ctl, HFrEF and HFrEF-cAF (Ctl: 13.6 ± 0.95 ms, HFrEF: 18.8 ± 4.2 ms, and HFrEF-cAF: 18.1 ± 1.2 ms), it was increased in cAF (20.7 ± 2.9 ms). The slow time constant was significantly larger in HFrEF-cAF patients (131.8 ± 12.1 ms) and slightly increased in HFrEF (90.1 ± 3.2 ms; P = 0.058) compared to Ctl patients (63.2 ± 2.2 ms; Figure 3E). Taken together, these data point to potential remodeling of atrial Ca2+ handling in patients with HFrEF and HFrEF-cAF.


FIGURE 3. L-type Ca2+ current (ICa,L) measurements in isolated human atrial cardiomyocytes. (A) Representative ICa,L recording during a 200-ms depolarizing pulse to +10 mV in a Ctl (black), HFrEF (blue), cAF (red) or HFrEF-cAF (blue/red) atrial cardiomyocyte (left) and quantification of ICaL amplitude (right). (B) Current-voltage relationship of peak ICa,L. (C) Representative examples of ICa,L inactivation protocol (left) and voltage dependence of inactivation (right) (D) midpoint of inactivation in Ctl, HFrEF, cAF and HFrEF-cAF patients. (E) Fast and slow time constants of inactivation during a depolarization to +10 mV in Ctl, HFrEF, cAF and HFrEF-cAF patients. (F) Representative examples (left) and quantification (right) of ICa,L recovery from inactivation with various interpulse intervals. Numbers in bars indicate number of cells/number of patients. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF, $ indicates P < 0.05 vs. cAF.

Ca2+-Handling Remodeling

We first assessed indices of dysfunctional diastolic Ca2+ handling by measuring spontaneous occurrence of depolarizing transient-inward currents at -80 mV with perforated patch-clamp technique (Figure 4A), as described (Hove-Madsen et al., 2004). These currents, which are mediated by NCX, represent a well-accepted proarrhythmic consequence of spontaneous SR Ca2+-release events (Hove-Madsen et al., 2004; Llach et al., 2011; Heijman et al., 2014). The frequency of spontaneous INCX was larger in HFrEF (2.3 ± 0.49 min-1), cAF (2.0 ± 0.41 min-1), and HFrEF-cAF (1.5 ± 0.42 min-1) compared to Ctl (0.51 ± 0.14 min-1; Figure 4B), with unchanged INCX amplitude between the groups (Figure 4C).


FIGURE 4. Spontaneous Ca2+-release events in isolated human atrial cardiomyocytes. (A) Representative recordings of NCX-mediated transient-inward current (INCX) in atrial cardiomyocytes from Ctl, HFrEF, cAF or HFrEF-cAF patients. (B,C) Frequency (B) and amplitude (C) of spontaneous INCX in the four groups. Numbers in bars indicate number of cells/number of patients. indicates P < 0.05 vs. Ctl.

Spontaneous SR Ca2+-release events could be promoted by an increased SR Ca2+ load. Therefore, we quantified SR Ca2+ load during caffeine-mediated SR Ca2+ release, which produces a large INCX, the integral of which is a reliable measure of SR Ca2+ content (Hove-Madsen et al., 2004; Voigt et al., 2012, 2014). SR Ca2+ load was significantly larger in HFrEF (10.1 ± 0.75 amol/pF) compared to Ctl (6.6 ± 0.50 amol/pF; P < 0.01; Figures 5A,B), but unchanged in cAF or HFrEF-cAF. The time constant of the caffeine-induced INCX was not different between the groups, pointing to an unaltered NCX function (Figure 5C). Accordingly, NCX1 protein expression was unchanged in HFrEF and HFrEF-cAF patients (Figure 6).


FIGURE 5. Sarcoplasmic reticulum (SR) Ca2+ load in isolated human atrial cardiomyocytes. (A) Representative recordings of NCX-mediated inward current (INCX) induced by caffeine (10 mmol/l) application in atrial cardiomyocytes from Ctl, HFrEF, cAF or HFrEF-cAF patients (top panels). The bottom panels show the integral of membrane current over time, the amplitude of which is an accepted index of SR Ca2+ load. (B,C) SR Ca2+ load (B) and time constant of caffeine-induced INCX (an indicator of NCX function) in the four groups. Numbers in bars indicate number of cells/number of patients. indicates P < 0.05 vs. Ctl.


FIGURE 6. Molecular determinants of increased sarcoplasmic reticulum (SR) Ca2+ load. (A) Representative Western blot examples of protein expression of Na+-Ca2+-exchanger type-1 (NCX1; full-length protein of 160 kDa with proteolytic fragment at 120 kDa), SR Ca2+-ATPase type-2a (SERCA2a) and its inhibitory regulators phospholamban (PLB; total PLB as well as Ser16- and Thr17-phosphorylated PLB) and sarcolipin (SLN). GAPDH was used as loading control. Ser16-PLB of HFrEF-cAF represents an extreme example. (B) Quantification of NCX1, SERCA2a, total PLB, Ser16- and Thr17-phosphorylated PLB, Ser16/total PLB, Thr17/total PLB, and SLN in right-atrial tissue homogenates of Ctl (white bars), HFrEF (blue bars) or HFrEF-cAF (red/blue-striped bars). Numbers in bars indicate number of patients. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF.

The increased SR Ca2+ load could be mediated by increased SR Ca2+ uptake via SERCA2a. Protein levels of SERCA2a were unchanged in HFrEF, but strongly increased in patients with HFrEF-cAF (Figure 6). Protein expression of the inhibitory SERCA2a regulator PLB, along with phosphorylation of PLB at the protein kinase-A site (Ser16) or the Ca2+/calmodulin-dependent protein kinase-II site (Thr17) were not different between Ctl, HFrEF and HFrEF-cAF patients (Figure 6). By contrast, expression of the atrial-specific SERCA2a inhibitor sarcolipin was decreased by ∼66% in HFrEF and by ∼72% in HFrEF-cAF (P < 0.05 vs. Ctl for both), likely increasing SR Ca2+ uptake.

Besides increased SR Ca2+ load, spontaneous SR Ca2+-release events often result from RyR2 dysfunction (Voigt et al., 2012, 2014; Beavers et al., 2013; Li et al., 2014). To address this directly we investigated RyR2 single-channel open probability in lipid bilayer experiments (Figure 7A). At 150 nmol/L intracellular [Ca2+], mimicking diastolic conditions, RyR2 open probability was significantly larger in both HFrEF (5.7 ± 1.6%) and HFrEF-cAF (30.9 ± 11.8%) patients compared to Ctl (0.6 ± 0.2%) patients (P < 0.05 for both; Figure 7B). The increased open probability was primarily due to a decrease in closed time (Figure 7D), although single-channel open time was significantly prolonged in HFrEF-cAF patients (Figure 7C), further increasing open probability. Finally, we assessed the molecular basis of the increased RyR2 open probability using Western blotting (Figure 8A). Compared to Ctl the relative RyR2 protein levels were decreased by ∼45% in HFrEF patients (P < 0.01), along with a similar non-significant trend (∼28% reduction) in HFrEF-cAF (P = 0.10; Figure 8B). Phosphorylation levels at Ser2808-RyR2 normalized to total RyR2 were not different between the three groups, whereas relative phosphorylation at Ser2814-RyR2 was increased by ∼97% in HFrEF-cAF compared to Ctl or HFrEF patients (P < 0.05 for both), potentially underlying the increased RyR2 open probability in these patients (Figure 8B). We also investigated the protein levels of other validated components of the RyR2 macromolecular complex (CSQ, junctin, and junctophilin-2) (Landstrom et al., 2017). Protein levels of CSQ were unchanged in HFrEF or HFrEF-cAF compared to Ctl (Figure 8C), whereas junctin expression was ∼65% higher in HFrEF vs Ctl patients (P = 0.011) and there was a trend toward increased levels of junctophilin-2 in HFrEF compared to Ctl patients (P = 0.059; Figure 8C).


FIGURE 7. Single-channel recordings of cardiac ryanodine receptor type-2 (RyR2) channels. (A) Representative RyR2 single-channel recording in a right-atrial sample from a Ctl, HFrEF or HFrEF-cAF patient. Upward deflections reflect channel opening. (B–D) Quantification of open probability (B), mean open time (C), and mean closed time (D) of single RyR2 channels from Ctl (white bars/symbols), HFrEF (blue bars/symbols) or HFrEF-cAF (red/blue-striped bars/symbols) patients. Numbers represent number of channels/number of patients. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF.


FIGURE 8. Molecular determinants of ryanodine receptor type-2 (RyR2) dysfunction. (A) Representative Western blot examples of total RyR2, Ser2808-, and Ser2814-phosphorylated RyR2 and calsequestrin (CSQ; left), as well as junctin and junctophilin-2 (JPH2; right) protein expression levels. GAPDH was used as loading control. (B) Quantification of total RyR2, Ser2808-, and Ser2814-phosphorylated RyR2, Ser2808/total RyR2, and Ser2814/total RyR2 protein expression levels in Ctl (white bars), HFrEF (blue bars) and HFrEF-cAF (red/blue-striped bars) patients. (C) Protein expression levels of the RyR2-interacting proteins CSQ, junctin, and JPH2 in Ctl, HFrEF and HFrEF-cAF patients. Data are shown relative to Ctl. Numbers in bars indicate number of patients. indicates P < 0.05 vs. Ctl, # indicates P < 0.05 vs. HFrEF.


In the present study, we have detailed for the first time profibrotic, electrical and Ca2+-handling remodeling in patients with HFrEF alone and HFrEF-cAF. Our data show (1) that profibrotic markers are upregulated in patients with HFrEF, independent of the presence of AF; (2) that protein expression and phosphorylation of connexin-43 are reduced in HFrEF only; (3) that classical indices of AF-related atrial electrical remodeling only occur in cAF and HFrEF-cAF; and (4) that potentially proarrhythmic atrial Ca2+-handling abnormalities are a typical finding in both HFrEF and HFrEF-cAF patients. Together, these data provide novel insights into the cellular and molecular mechanisms of AF in patients with HFrEF and HFrEF-cAF, which may have important implications for the development of novel therapeutic option for AF patients in the context of HF.

Comparison to Previous Work

Atrial structural remodeling is a consistent finding in patients with HFrEF. At the tissue level, increased atrial fibrosis assessed using late gadolinium enhancement magnetic resonance imaging has been reported (Akkaya et al., 2013). Atrial fibrosis is also a common finding in animal models of HFrEF (Li et al., 1999; Milliez et al., 2005; Yamada et al., 2017; Pluteanu et al., 2018), and the underlying pathways have been investigated in detail (Cardin et al., 2003). Our data similarly point to prominent profibrotic remodeling, with increased expression of col1a, periostin and fibronectin. The associated alterations in atrial structure are expected to cause reentry-promoting slow, heterogeneous conduction, which has been directly observed in vivo in atria of HFrEF patients (Sanders et al., 2003). We also identified reduced expression and Ser368 phosphorylation of Cx43 in HFrEF patients, which may also contribute to conduction abnormalities.

Reentry-promoting electrical remodeling, characterized by shortening of APD and hyperpolarization of the resting membrane potential, is a hallmark of cAF and is a consistent finding in animal models with atrial tachycardia remodeling (Heijman et al., 2014). By contrast, APD and resting membrane potential of patients with paroxysmal AF are not different from Ctl patients (Voigt et al., 2014; Schmidt et al., 2015). Similarly, in the present study we found no significant differences in AP properties in patients with HFrEF only, suggesting that electrical remodeling may be primarily a consequence of the rapid atrial rate during cAF. At the cardiomyocyte level various inconsistent results have been published about atrial electrical remodeling in the setting of HF. Workman et al. (2009) reported shortened APD and effective refractory period (ERP) in atrial cardiomyocytes from HFrEF patients undergoing cardiac surgery, whereas Schreieck et al. (2000) detected no differences in atrial cardiomyocyte APD between HFrEF and Ctl patients or healthy donors. Finally, other studies in atrial cardiomyocytes (Koumi et al., 1994), ex vivo multicellular preparations (Fedorov et al., 2011) and in vivo recordings in patients (Sanders et al., 2003) have reported prolonged APD and/or ERP.

The inconsistent results between studies related to APD in HFrEF patients might at least in part be explained by the use of isolated cardiomyocytes vs. multicellular preparations and the techniques used to assess APD/ERP. Cardiomyocyte isolation procedures from human atria are known to affect function of a number of ion channels, often resulting in depolarized resting membrane potentials that require injection of a hyperpolarizing current in order to record APs. Such a current may differentially affect APs from Ctl or HFrEF patients. In addition, remodeling of individual ion currents in HFrEF patients appears highly variable between studies. For example, both reduced and unchanged inward-rectifier K+ current, as well as reduced, unchanged and increased transient-outward K+ current have been reported (Koumi et al., 1994; Van Wagoner et al., 1997; Schreieck et al., 2000; Workman et al., 2009). Differences in patient characteristics, including the use of explanted end-stage failing hearts and healthy donor hearts in some studies (Koumi et al., 1994; Van Wagoner et al., 1997; Fedorov et al., 2011), compared to patients undergoing open-heart surgery with normal or impaired LV function in our and other studies (Schreieck et al., 2000; Workman et al., 2009), may also contribute to the variable findings. Similarly, work from animal models suggest that the duration of HF differentially affects electrical remodeling, with 2 weeks of ventricular tachypacing resulting in ERP prolongation (Cha et al., 2004), 5 weeks of ventricular tachypacing associating with unchanged ERP (Li et al., 1999) and 4 months of ventricular tachypacing abbreviating atrial ERP (Sridhar et al., 2009). Since the duration of HFrEF is usually not controlled in patients, differences in HFrEF duration between the human studies are expected. Here we employed sharp-electrode AP recordings in multicellular preparations, which avoided cell-isolation-induced effects, minimized the variability in individual ion currents and produced stable resting membrane potentials at physiological levels. Our results suggest that even if remodeling in some ion currents might exist in HFrEF patients, resting membrane potential and APD shape do not differ between Ctl and HFrEF patients. Clearly, validation of our multicellular findings in other patient cohorts is needed to confirm whether alterations in atrial APD occur with HFrEF.

Our current data indicate that also in the presence of HFrEF, AF produces typical atrial tachycardia-related remodeling, including reentry-promoting APD shortening. These data are consistent with results from Cha et al. who showed that atrial tachycardia shortened ERP in dogs with pacing-induced HF, albeit to a lesser degree than dogs with normal LV function (Cha et al., 2004). By contrast, in a pig model the combined presence of AF and HF resulted in prolonged APD (Lugenbiel et al., 2015). However, in this model AF was the primary initiator of a (mild) ventricular tachycardiomyopathy, which is different from patients in whom HF is mainly due to advanced cardiovascular disease, notably hypertension and myocardial infarction (Benjamin et al., 2018), as in our study. Overall, despite the fact that potential APD changes can occur with HFrEF, once AF develops it produces the APD shortening that typifies the electrophysiological profile in patients with cAF.

To the best of our knowledge, functional Ca2+-handling remodeling has not been studied in atria of patients with HFrEF. Here we identified extensive indices of abnormal Ca2+-handling in these patients, both in the absence and presence of AF, including greater incidence of spontaneous INCX, increased SR Ca2+ load, and RyR2 dysfunction. Protein levels of sarcolipin and RyR2 were decreased in HFrEF patients, but we did not find significant changes in SERCA2a or NCX1 expression, PLB expression or phosphorylation, or RyR2 phosphorylation in these patients. Our results are consistent with data from Shanmugam et al. (2011) who also identified decreased sarcolipin expression, unchanged SERCA2a expression and a tendency toward decreased RyR2 expression in atria from HF patients. The present results are also in line with data in atrial cardiomyocytes from rabbits with chronic myocardial infarction (Kettlewell et al., 2013), failing hearts from spontaneously hypertensive rats (Pluteanu et al., 2018), and a dog model of ventricular tachypacing-induced HF (Stambler et al., 2003; Yeh et al., 2008), all of which showed an increased incidence of spontaneous SR Ca2+-release events. Moreover, HF dogs also had increased SR Ca2+ load, decreased RyR2 expression, unaltered RyR2 phosphorylation and unchanged expression of PLB or NCX1 (Yeh et al., 2008), similar to our data. In contrast to our findings, SERCA2a expression was decreased in this model and the significantly increased SR Ca2+ load was explained by an increase in PLB phosphorylation at Thr17 (Yeh et al., 2008). Finally, our data in HFrEF patients are similar to our previous findings in patients with paroxysmal AF (Voigt et al., 2014). Paroxysmal AF patients also exhibited increased SR Ca2+ load and spontaneous SR Ca2+-release events, although the underlying molecular mechanisms appear somewhat distinct, involving increased RyR2 expression and decreased SERCA2a expression. Interestingly, despite a similar functional phenotype, there also appear to be mechanistic differences at the molecular level between HFrEF and HFrEF-cAF patients. For example, although protein levels of sarcolipin and RyR2 are decreased in both HFrEF and HFrEF-cAF patients, only the latter group have upregulated SERCA2a expression along with increased RyR2-Ser2814 phosphorylation, which sensitizes RyR2 to cytosolic Ca2+. The higher RyR2-Ser2814 phosphorylation level is consistent with the significantly greater RyR2 single-channel open probability in HFrEF-cAF compared to Ctl or HFrEF patients, likely explaining why SR Ca2+ load is not increased in HFrEF-cAF. The increased SERCA2a expression might also help to maintain SR Ca2+ load despite the strong increase in RyR2 open probability, which is expected to increase SR Ca2+ leak and to decrease SR Ca2+ load. Finally, protein levels of junctin were higher in HFrEF, but not HFrEF-cAF patients and mice with cardiac restricted junctin overexpression develop spontaneous AF (Hong et al., 2002). Thus junctin-mediated RyR2 dysfunction might contribute to the development of AF in the context of HF.

Clinical Implications

Despite the important progress being made in our understanding, diagnosis and treatment of AF, it remains a major clinical problem (Heijman et al., 2018). Basic science has provided a lot of insights about the fundamental mechanisms underlying AF, identifying ectopic (triggered) activity promoted by Ca2+-handling abnormalities and reentry promoted by APD shortening and slow, heterogeneous conduction as the major arrhythmia mechanisms (Heijman et al., 2014, 2016). Nonetheless, a number of important translational challenges remain (Heijman et al., 2018), including the identification of the dominant arrhythmia mechanisms in specific subgroups of AF patients to enable tailored therapy. There is increasing awareness that AF is a common endpoint of many different pathophysiological processes that promote an atrial cardiomyopathy (Andrade et al., 2014; Goette et al., 2017). However, the nature of the underlying atrial remodeling is likely distinct for different comorbidities, risk factors and stages of the disease. In agreement, we have previously shown that there are important differences in atrial remodeling between patients with paroxysmal AF and those with cAF (Voigt et al., 2012, 2014; Beavers et al., 2013). Atrial remodeling in patients with HFrEF or HFrEF-cAF has not previously been characterized in detail, particularly with respect to atrial Ca2+-handling, despite the very common clinical coexistence of AF and HF (Ling et al., 2016; Sartipy et al., 2017).

Together with previous studies, our current data suggest that Ca2+-handling abnormalities and Ca2+-mediated triggered activity are a common motif shared by cAF patients and HF patients in sinus rhythm, who are at an increased risk of developing AF. Atrial arrhythmias have a focal initiation pattern in dogs with ventricular tachypacing-induced HF (Fenelon et al., 2003) and their inducibility is suppressed by Ca2+-antagonists (Stambler et al., 2003), supporting a major role for Ca2+-mediated ectopic activity in the initiation of AF in the setting of HF. In addition, there is evidence for a significant role of focal ectopy in AF patients (Haissaguerre et al., 1998; Lee et al., 2015).

Accumulating evidence suggests that Ca2+-handling abnormalities may promote structural remodeling. For example, CREM-IbΔC-X transgenic mice develop progressive atrial remodeling and spontaneous AF, which is prevented by genetic inhibition of RyR2 dysfunction and associated SR Ca2+ leak (Li et al., 2014). Similarly, the PLB-R14del mutation produces Ca2+-handling abnormalities and exhibits a clinical phenotype characterized initially by an increased risk of ventricular arrhythmias at young age, with a subsequent predisposition to dilated cardiomyopathy and HF (van Rijsingen et al., 2014). Thus, abnormal Ca2+-handling might be an early event in the pathogenesis of AF, apart from promotion of ectopic activity per se. In particular, the HFrEF-induced atrial Ca2+-handling remodeling that we identified may serve both as an initiator of AF episodes and a promoter of atrial electrical and structural remodeling, creating a substrate for the maintenance and progression of AF. Thus, our present findings may have important clinical implications. They point to an urgent need for methods to assess potential cardiomyocyte Ca2+-handling abnormalities in patients during the early stages of the remodeling process, when the disease is still amenable to therapy, and a need for better therapeutic options to treat these abnormalities based on our understanding of the underlying molecular mechanisms in specific patient subgroups (Heijman et al., 2018). Moreover, since atrial Ca2+-handling remodeling in HFrEF patients is characterized by both RyR2 and SERCA2a dysfunction, a therapeutic intervention modulating only a single target may not be sufficient to normalize altered atrial Ca2+ handling. Indeed, we have previously shown in paroxysmal AF patients with a similar phenotype that RyR2 and SERCA2a dysfunction can each promote proarrhythmic spontaneous SR Ca2+-release events and that the combination of both factors is significantly more proarrhythmic than each individually (Voigt et al., 2014). Technological advances such as catheter-based photoacoustic imaging with cell-permeable Ca2+ indicators (Roberts et al., 2018) may in the future enable in vivo imaging of Ca2+-handling abnormalities in large animal models or patients (Heijman et al., 2018).

Potential Limitations

Although our data provide an extensive characterization of atrial remodeling in HFrEF and HFrEF-cAF patients, we did not address ion-channel remodeling in detail. Despite absence of AP changes in multicellular preparations, ICa,L was reduced in HFrEF patients, in line with previous findings (Ouadid et al., 1995). Thus, alterations in K+ channels may balance the reduction in ICa,L, resulting in unaltered AP properties, as previously observed in other studies (Koumi et al., 1994; Schreieck et al., 2000; Workman et al., 2009).

We did not measure Ca2+-handling abnormalities directly using Ca2+ imaging with fluorescent indicators. Instead, we employed spontaneous INCX during voltage-clamp at -80 mV as an accepted marker of spontaneous SR-derived Ca2+ release and we characterized Ca2+-handling remodeling through changes in RyR2 single-channel properties. Of note, the use of perforated-patch techniques with preserved physiological intracellular milieu, along with the absence of fluorescent Ca2+ indicators, which buffer intracellular Ca2+, are expected to result in a more precise detection of the consequences of abnormal SR Ca2+ releases. Nevertheless, subsequent work employing Ca2+ imaging should further dissect the precise abnormalities of atrial Ca2+-handling in the context of HFrEF with and without AF.

The present work is necessarily restricted to RA appendage tissue obtained from patients undergoing open-heart surgery. Our findings may not hold for other regions of the atria, which may be exposed to different levels of stretch or neurohumoral factors, and may not be applicable to HFrEF patients without an indication for open-heart surgery.

We have previously shown that there are important differences in Ca2+-handling abnormalities between paroxysmal AF and cAF (Voigt et al., 2012, 2014). Similarly, there are notable differences in the epidemiology, pathophysiology and therapeutic management of HF patients with reduced, mid-range and preserved LV ejection fraction, although AF is common in all variants (Lam and Solomon, 2014; Sartipy et al., 2017). Our results were obtained in patients with significantly impaired LV function (mean LV ejection fractions ∼30%) with or without cAF. Although the clinical characteristics of the HFrEF population employed in this population make an ischemic etiology very likely, we were unable to establish the exact etiology of HF for individual patients. Results might be different for other types of AF and HF, which could produce distinct forms of atrial remodeling and show complex patterns in their interaction. Furthermore, there were some differences in clinical characteristics (e.g., regarding the indication for surgery) among the patient groups and the different data sets for the same subgroup (i.e., between Tables 13), which might influence our findings. Finally, our study is concerned with the potential molecular and cellular mechanisms of AF in HFrEF patients, but although we were able to include data from cAF without HFrEF in our functional analyses, we did not have samples from cAF patients without HFrEF to include in the Western-blot experiments. Furthermore, our work does not address the additional tissue-level properties, such as fibrosis and conduction velocity patterns or autonomic innervation, which play a key role in cardiac arrhythmogenesis in patients. For example, we did not observe significant differences in maximum dV/dtmax (reflecting Na+-channel function) and conduction time, which also reflects connexin function, in multicellular preparations of HFrEF patients, despite reduced Cx43 protein levels and reports of reduced conduction velocity in vivo (Sanders et al., 2003), suggesting a role for regional differences and additional regulatory mechanisms of atrial conduction in the intact heart.


In this study, we provide the first detailed characterization of atrial remodeling in the setting of HFrEF with and without cAF. Spontaneous INCX currents, likely mediated by Ca2+-handling abnormalities, are increased and might act as triggers of AF in HFrEF patients with profibrotic and connexin remodeling. AF subsequently produces atrial electrical remodeling that stabilizes the arrhythmia by promoting AF-maintaining reentry. These novel findings may have important implications for the development of new treatment options for AF in the context of HF.

Author Contributions

CM and DD conceived the research. CM, IA-T, and QW performed the experiments. ER-D and MK provided reagents and samples. CM, IA-T, QW, SN, UR, XW, JH, and DD analyzed the data. XW, LH-M, and DD handled funding and project management. JH, SN, and DD drafted and revised the manuscript. All authors approved the final version of the manuscript.


This work was supported by Marie Curie IEF Grant (PIEF-GA-2012-331241 to CM), the Netherlands Organization for Scientific Research (ZonMW Veni 91616057 to JH), the National Institutes of Health (R01-HL131517 and R01-HL136389 to DD; and R01-HL089598, R01-HL-091947, R01-HL117641, and R01-HL134824 to XW), the DZHK (German Center for Cardiovascular Research, 81X2800108, 81X2800161, and 81X2800136 to DD), Spanish Ministry for Science, Innovation and Universities (SAF2014-58286-C2-1-R and SAF2017-88019-C3-1-R to LH-M) and Marató TV3 foundation (2015-2-30 to LH-M) and the German Research Foundation (DFG, Do 769/4-1 to DD), and the Canadian Institutes of Health Research (1484011) and Heart and Stroke Foundation of Canada (16-12708) to SN.

Conflict of Interest Statement

XW is a founding partner of Elex Biotech, a start-up company that developed drug molecules that target ryanodine receptors for the treatment of cardiac arrhythmia disorders. DD is a member of the scientific advisory board of OMEICOS Therapeutics GmbH, a company developing small molecules mimicking the effects of omega-3 fatty acids, and of Acesion Pharma, a company developing selective blockers of small-conductance calcium dependent potassium channels.

The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.


The authors thank Ramona Nagel and Konstanze Fischer for excellent technical assistance.


AF, atrial fibrillation; AP, action potential; APD, AP duration; αSMA, α smooth muscle actin; cAF, long-standing persistent (‘chronic’) AF; Col1a, collagen 1a; CSQ, calsequestrin; Cx40/43, connexin-40/connexin-43; ERP, effective refractory period; HF, heart failure; HFrEF, heart failure with reduced ejection fraction; ICa,L, L-type Ca2+ current; ITI, transient-inward current; LV, left ventricle; MMP9, matrix metallopeptidase 9; NCX1, Na+-Ca2+-exchanger type-1; NYHA, New York Heart Association; PLB, phospholamban; RA, right atrium; RyR2, ryanodine receptor type-2; SERCA2a, sarcoplasmic reticulum Ca2+-ATPase type-2a; SR, sarcoplasmic reticulum; TGF-β1, transforming growth factor β1.


Akkaya, M., Higuchi, K., Koopmann, M., Damal, K., Burgon, N. S., Kholmovski, E., et al. (2013). Higher degree of left atrial structural remodeling in patients with atrial fibrillation and left ventricular systolic dysfunction. J. Cardiovasc. Electrophysiol. 24, 485–491. doi: 10.1111/jce.12090

PubMed Abstract | CrossRef Full Text | Google Scholar

Andrade, J., Khairy, P., Dobrev, D., and Nattel, S. (2014). The clinical profile and pathophysiology of atrial fibrillation: relationships among clinical features, epidemiology, and mechanisms. Circ. Res. 114, 1453–1468. doi: 10.1161/CIRCRESAHA.114.303211

PubMed Abstract | CrossRef Full Text | Google Scholar

Beavers, D. L., Wang, W., Ather, S., Voigt, N., Garbino, A., Dixit, S. S., et al. (2013). Mutation E169K in junctophilin-2 causes atrial fibrillation due to impaired RyR2 stabilization. J. Am. Coll. Cardiol. 62, 2010–2019. doi: 10.1016/j.jacc.2013.06.052

PubMed Abstract | CrossRef Full Text | Google Scholar

Benjamin, E. J., Virani, S. S., Callaway, C. W., Chamberlain, A. M., Chang, A. R., Cheng, S., et al. (2018). Heart disease and stroke statistics-2018 update: a report from the American heart association. Circulation 137, e67–e492. doi: 10.1161/CIR.0000000000000558

PubMed Abstract | CrossRef Full Text | Google Scholar

Brundel, B. J., Henning, R. H., Kampinga, H. H., Van Gelder, I. C., and Crijns, H. J. (2002). Molecular mechanisms of remodeling in human atrial fibrillation. Cardiovasc. Res. 54, 315–324.

Google Scholar

Cao, H., Xue, L., Wu, Y., Ma, H., Chen, L., Wang, X., et al. (2010). Natriuretic peptides and right atrial fibrosis in patients with paroxysmal versus persistent atrial fibrillation. Peptides 31, 1531–1539. doi: 10.1016/j.peptides.2010.04.019

PubMed Abstract | CrossRef Full Text | Google Scholar

Cardin, S., Li, D., Thorin-Trescases, N., Leung, T. K., Thorin, E., and Nattel, S. (2003). Evolution of the atrial fibrillation substrate in experimental congestive heart failure: angiotensin-dependent and -independent pathways. Cardiovasc. Res. 60, 315–325.

PubMed Abstract | Google Scholar

Cha, T. J., Ehrlich, J. R., Zhang, L., and Nattel, S. (2004). Atrial ionic remodeling induced by atrial tachycardia in the presence of congestive heart failure. Circulation 110, 1520–1526. doi: 10.1161/01.CIR.0000142052.03565.87

PubMed Abstract | CrossRef Full Text | Google Scholar

Cone, A. C., Cavin, G., Ambrosi, C., Hakozaki, H., Wu-Zhang, A. X., Kunkel, M. T., et al. (2014). Protein kinase Cδ-mediated phosphorylation of Connexin43 gap junction channels causes movement within gap junctions followed by vesicle internalization and protein degradation. J. Biol. Chem. 289, 8781–8798. doi: 10.1074/jbc.M113.533265

PubMed Abstract | CrossRef Full Text | Google Scholar

Dobrev, D., Graf, E., Wettwer, E., Himmel, H. M., Hala, O., Doerfel, C., et al. (2001). Molecular basis of downregulation of G-protein-coupled inward rectifying K+ current (IK,ACh) in chronic human atrial fibrillation: decrease in GIRK4 mRNA correlates with reduced IK,ACh and muscarinic receptor–mediated shortening of action potentials. Circulation 104, 2551–2557.

Google Scholar

El-Armouche, A., Boknik, P., Eschenhagen, T., Carrier, L., Knaut, M., Ravens, U., et al. (2006). Molecular determinants of altered Ca2+ handling in human chronic atrial fibrillation. Circulation 114, 670–680. doi: 10.1161/CIRCULATIONAHA.106.636845

PubMed Abstract | CrossRef Full Text | Google Scholar

Fedorov, V. V., Glukhov, A. V., Ambrosi, C. M., Kostecki, G., Chang, R., Janks, D., et al. (2011). Effects of KATP channel openers diazoxide and pinacidil in coronary-perfused atria and ventricles from failing and non-failing human hearts. J. Mol. Cell Cardiol. 51, 215–225. doi: 10.1016/j.yjmcc.2011.04.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Fenelon, G., Shepard, R. K., and Stambler, B. S. (2003). Focal origin of atrial tachycardia in dogs with rapid ventricular pacing-induced heart failure. J. Cardiovasc. Electrophysiol. 14, 1093–1102.

Google Scholar

Goette, A., Kalman, J. M., Aguinaga, L., Akar, J., Cabrera, J. A., Chen, S. A., et al. (2017). EHRA/HRS/APHRS/SOLAECE expert consensus on atrial cardiomyopathies: Definition, characterization, and clinical implication. Heart Rhythm 14, e3–e40. doi: 10.1016/j.hrthm.2016.05.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Haissaguerre, M., Jais, P., Shah, D. C., Takahashi, A., Hocini, M., Quiniou, G., et al. (1998). Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins. N. Engl. J. Med. 339, 659–666. doi: 10.1056/NEJM199809033391003

PubMed Abstract | CrossRef Full Text | Google Scholar

Heijman, J., Algalarrondo, V., Voigt, N., Melka, J., Wehrens, X. H., Dobrev, D., et al. (2016). The value of basic research insights into atrial fibrillation mechanisms as a guide to therapeutic innovation: a critical analysis. Cardiovasc. Res. 109, 467–479. doi: 10.1093/cvr/cvv275

PubMed Abstract | CrossRef Full Text | Google Scholar

Heijman, J., Guichard, J. B., Dobrev, D., and Nattel, S. (2018). Translational challenges in atrial fibrillation. Circ. Res. 122, 752–773. doi: 10.1161/CIRCRESAHA.117.311081

PubMed Abstract | CrossRef Full Text | Google Scholar

Heijman, J., Voigt, N., Abu-Taha, I. H., and Dobrev, D. (2013). Rhythm control of atrial fibrillation in heart failure. Heart Fail. Clin. 9, 407–415. doi: 10.1016/j.hfc.2013.06.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Heijman, J., Voigt, N., Nattel, S., and Dobrev, D. (2014). Cellular and molecular electrophysiology of atrial fibrillation initiation, maintenance, and progression. Circ. Res. 114, 1483–1499. doi: 10.1161/CIRCRESAHA.114.302226

PubMed Abstract | CrossRef Full Text | Google Scholar

Hohendanner, F., Messroghli, D., Bode, D., Blaschke, F., Parwani, A., Boldt, L. H., et al. (2018). Atrial remodelling in heart failure: recent developments and relevance for heart failure with preserved ejection fraction. ESC Heart Fail. 5, 211–221. doi: 10.1002/ehf2.12260

PubMed Abstract | CrossRef Full Text | Google Scholar

Hong, C. S., Cho, M. C., Kwak, Y. G., Song, C. H., Lee, Y. H., Lim, J. S., et al. (2002). Cardiac remodeling and atrial fibrillation in transgenic mice overexpressing junction. FASEB J. 16, 1310–1312. doi: 10.1096/fj.01-0908fje

PubMed Abstract | CrossRef Full Text | Google Scholar

Hove-Madsen, L., Llach, A., Bayes-Genis, A., Roura, S., Rodriguez Font, E., Aris, A., et al. (2004). Atrial fibrillation is associated with increased spontaneous calcium release from the sarcoplasmic reticulum in human atrial myocytes. Circulation 110, 1358–1363. doi: 10.1161/01.CIR.0000141296.59876.87

PubMed Abstract | CrossRef Full Text | Google Scholar

Jalife, J., and Kaur, K. (2015). Atrial remodeling, fibrosis, and atrial fibrillation. Trends Cardiovasc. Med. 25, 475–484. doi: 10.1016/j.tcm.2014.12.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Kettlewell, S., Burton, F. L., Smith, G. L., and Workman, A. J. (2013). Chronic myocardial infarction promotes atrial action potential alternans, afterdepolarizations, and fibrillation. Cardiovasc. Res. 99, 215–224. doi: 10.1093/cvr/cvt087

PubMed Abstract | CrossRef Full Text | Google Scholar

Koumi, S., Arentzen, C. E., Backer, C. L., and Wasserstrom, J. A. (1994). Alterations in muscarinic K+ channel response to acetylcholine and to G protein-mediated activation in atrial myocytes isolated from failing human hearts. Circulation 90, 2213–2224.

Google Scholar

Lam, C. S., and Solomon, S. D. (2014). The middle child in heart failure: heart failure with mid-range ejection fraction (40-50%). Eur. J. Heart Fail. 16, 1049–1055. doi: 10.1002/ejhf.159

PubMed Abstract | CrossRef Full Text | Google Scholar

Landstrom, A. P., Dobrev, D., and Wehrens, X. H. T. (2017). Calcium signaling and cardiac arrhythmias. Circ. Res. 120, 1969–1993. doi: 10.1161/CIRCRESAHA.117.310083

PubMed Abstract | CrossRef Full Text | Google Scholar

Lee, S., Sahadevan, J., Khrestian, C. M., Cakulev, I., Markowitz, A., and Waldo, A. L. (2015). Simultaneous biatrial high-density (510-512 electrodes) epicardial mapping of persistent and long-standing persistent atrial fibrillation in patients: new insights into the mechanism of its maintenance. Circulation 132, 2108–2117. doi: 10.1161/CIRCULATIONAHA.115.017007

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, D., Fareh, S., Leung, T. K., and Nattel, S. (1999). Promotion of atrial fibrillation by heart failure in dogs: atrial remodeling of a different sort. Circulation 100, 87–95.

PubMed Abstract | Google Scholar

Li, D., Melnyk, P., Feng, J., Wang, Z., Petrecca, K., Shrier, A., et al. (2000). Effects of experimental heart failure on atrial cellular and ionic electrophysiology. Circulation 101, 2631–2638.

Google Scholar

Li, N., Chiang, D. Y., Wang, S., Wang, Q., Sun, L., Voigt, N., et al. (2014). Ryanodine receptor-mediated calcium leak drives progressive development of an atrial fibrillation substrate in a transgenic mouse model. Circulation 129, 1276–1285. doi: 10.1161/CIRCULATIONAHA.113.006611

PubMed Abstract | CrossRef Full Text | Google Scholar

Ling, L. H., Kistler, P. M., Kalman, J. M., Schilling, R. J., and Hunter, R. J. (2016). Comorbidity of atrial fibrillation and heart failure. Nat. Rev. Cardiol. 13, 131–147. doi: 10.1038/nrcardio.2015.191

PubMed Abstract | CrossRef Full Text | Google Scholar

Llach, A., Molina, C. E., Prat-Vidal, C., Fernandes, J., Casado, V., Ciruela, F., et al. (2011). Abnormal calcium handling in atrial fibrillation is linked to up-regulation of adenosine A2A receptors. Eur. Heart J. 32, 721–729. doi: 10.1093/eurheartj/ehq464

PubMed Abstract | CrossRef Full Text | Google Scholar

Loose, S., Mueller, J., Wettwer, E., Knaut, M., Ford, J., Milnes, J., et al. (2014). Effects of IKur blocker MK-0448 on human right atrial action potentials from patients in sinus rhythm and in permanent atrial fibrillation. Front. Pharmacol. 5:26. doi: 10.3389/fphar.2014.00026

CrossRef Full Text | Google Scholar

Lugenbiel, P., Wenz, F., Govorov, K., Schweizer, P. A., Katus, H. A., and Thomas, D. (2015). Atrial fibrillation complicated by heart failure induces distinct remodeling of calcium cycling proteins. PLoS One 10:e0116395. doi: 10.1371/journal.pone.0116395

PubMed Abstract | CrossRef Full Text | Google Scholar

Marrouche, N. F., Brachmann, J., Andresen, D., Siebels, J., Boersma, L., Jordaens, L., et al. (2018). Catheter ablation for atrial fibrillation with heart failure. N. Engl. J. Med. 378, 417–427. doi: 10.1056/NEJMoa1707855

PubMed Abstract | CrossRef Full Text | Google Scholar

Milliez, P., Deangelis, N., Rucker-Martin, C., Leenhardt, A., Vicaut, E., Robidel, E., et al. (2005). Spironolactone reduces fibrosis of dilated atria during heart failure in rats with myocardial infarction. Eur. Heart J. 26, 2193–2199. doi: 10.1093/eurheartj/ehi478

PubMed Abstract | CrossRef Full Text | Google Scholar

Mogensen, U. M., Jhund, P. S., Abraham, W. T., Desai, A. S., Dickstein, K., Packer, M., et al. (2017). Type of atrial fibrillation and outcomes in patients with heart failure and reduced ejection fraction. J. Am. Coll. Cardiol. 70, 2490–2500. doi: 10.1016/j.jacc.2017.09.027

PubMed Abstract | CrossRef Full Text | Google Scholar

Molina, C. E., Leroy, J., Richter, W., Xie, M., Scheitrum, C., Lee, I. O., et al. (2012). Cyclic adenosine monophosphate phosphodiesterase type 4 protects against atrial arrhythmias. J. Am. Coll. Cardiol. 59, 2182–2190. doi: 10.1016/j.jacc.2012.01.060

PubMed Abstract | CrossRef Full Text | Google Scholar

Ouadid, H., Albat, B., and Nargeot, J. (1995). Calcium currents in diseased human cardiac cells. J. Cardiovasc. Pharmacol. 25, 282–291.

Google Scholar

Pandit, S. V., and Workman, A. J. (2016). Atrial electrophysiological remodeling and fibrillation in heart failure. Clin. Med. Insights Cardiol. 10(Suppl 1), 41–46. doi: 10.4137/CMC.S39713

PubMed Abstract | CrossRef Full Text | Google Scholar

Pluteanu, F., Nikonova, Y., Holzapfel, A., Herzog, B., Scherer, A., Preisenberger, J., et al. (2018). Progressive impairment of atrial myocyte function during left ventricular hypertrophy and heart failure. J. Mol. Cell Cardiol. 114, 253–263. doi: 10.1016/j.yjmcc.2017.11.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Polyakova, V., Miyagawa, S., Szalay, Z., Risteli, J., and Kostin, S. (2008). Atrial extracellular matrix remodelling in patients with atrial fibrillation. J. Cell Mol. Med. 12, 189–208. doi: 10.1111/j.1582-4934.2008.00219.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Roberts, S., Seeger, M., Jiang, Y., Mishra, A., Sigmund, F., Stelzl, A., et al. (2018). Calcium sensor for photoacoustic imaging. J. Am. Chem. Soc. 140, 2718–2721. doi: 10.1021/jacs.7b03064

PubMed Abstract | CrossRef Full Text | Google Scholar

Sanders, P., Morton, J. B., Davidson, N. C., Spence, S. J., Vohra, J. K., Sparks, P. B., et al. (2003). Electrical remodeling of the atria in congestive heart failure: electrophysiological and electroanatomic mapping in humans. Circulation 108, 1461–1468. doi: 10.1161/01.CIR.0000090688.49283.67

PubMed Abstract | CrossRef Full Text | Google Scholar

Sartipy, U., Dahlstrom, U., Fu, M., and Lund, L. H. (2017). Atrial fibrillation in heart failure with preserved, mid-range, and reduced ejection fraction. JACC Heart Fail. 5, 565–574. doi: 10.1016/j.jchf.2017.05.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmidt, C., Wiedmann, F., Voigt, N., Zhou, X. B., Heijman, J., Lang, S., et al. (2015). Upregulation of K2P3.1 K+ current causes action potential shortening in patients with chronic atrial fibrillation. Circulation 132, 82–92. doi: 10.1161/CIRCULATIONAHA.114.012657

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmidt, C., Wiedmann, F., Zhou, X. B., Heijman, J., Voigt, N., Ratte, A., et al. (2017). Inverse remodelling of K2P3.1 K+ channel expression and action potential duration in left ventricular dysfunction and atrial fibrillation: implications for patient-specific antiarrhythmic drug therapy. Eur. Heart J. 38, 1764–1774. doi: 10.1093/eurheartj/ehw559

PubMed Abstract | CrossRef Full Text | Google Scholar

Schotten, U., Verheule, S., Kirchhof, P., and Goette, A. (2011). Pathophysiological mechanisms of atrial fibrillation: a translational appraisal. Physiol. Rev. 91, 265–325. doi: 10.1152/physrev.00031.2009

PubMed Abstract | CrossRef Full Text | Google Scholar

Schreieck, J., Wang, Y., Overbeck, M., Schomig, A., and Schmitt, C. (2000). Altered transient outward current in human atrial myocytes of patients with reduced left ventricular function. J. Cardiovasc. Electrophysiol. 11, 180–192.

PubMed Abstract | Google Scholar

Shanmugam, M., Molina, C. E., Gao, S., Severac-Bastide, R., Fischmeister, R., and Babu, G. J. (2011). Decreased sarcolipin protein expression and enhanced sarco(endo)plasmic reticulum Ca2+ uptake in human atrial fibrillation. Biochem. Biophys. Res. Commun. 410, 97–101. doi: 10.1016/j.bbrc.2011.05.113

PubMed Abstract | CrossRef Full Text | Google Scholar

Sikkel, M. B., Francis, D. P., Howard, J., Gordon, F., Rowlands, C., Peters, N. S., et al. (2017). Hierarchical statistical techniques are necessary to draw reliable conclusions from analysis of isolated cardiomyocyte studies. Cardiovasc. Res. 113, 1743–1752. doi: 10.1093/cvr/cvx151

PubMed Abstract | CrossRef Full Text | Google Scholar

Simon, J. N., Ziberna, K., and Casadei, B. (2016). Compromised redox homeostasis, altered nitroso-redox balance, and therapeutic possibilities in atrial fibrillation. Cardiovasc. Res. 109, 510–518. doi: 10.1093/cvr/cvw012

PubMed Abstract | CrossRef Full Text | Google Scholar

Sridhar, A., Nishijima, Y., Terentyev, D., Khan, M., Terentyeva, R., Hamlin, R. L., et al. (2009). Chronic heart failure and the substrate for atrial fibrillation. Cardiovasc. Res. 84, 227–236. doi: 10.1093/cvr/cvp216

PubMed Abstract | CrossRef Full Text | Google Scholar

Stambler, B. S., Fenelon, G., Shepard, R. K., Clemo, H. F., and Guiraudon, C. M. (2003). Characterization of sustained atrial tachycardia in dogs with rapid ventricular pacing-induced heart failure. J. Cardiovasc. Electrophysiol. 14, 499–507.

PubMed Abstract | Google Scholar

van Rijsingen, I. A., Van Der Zwaag, P. A., Groeneweg, J. A., Nannenberg, E. A., Jongbloed, J. D., Zwinderman, A. H., et al. (2014). Outcome in phospholamban R14del carriers: results of a large multicentre cohort study. Circ. Cardiovasc. Genet. 7, 455–465. doi: 10.1161/CIRCGENETICS.113.000374

PubMed Abstract | CrossRef Full Text | Google Scholar

Van Wagoner, D. R., Pond, A. L., Mccarthy, P. M., Trimmer, J. S., and Nerbonne, J. M. (1997). Outward K+ current densities and Kv1.5 expression are reduced in chronic human atrial fibrillation. Circ. Res. 80, 772–781.

Google Scholar

Voigt, N., Heijman, J., Wang, Q., Chiang, D. Y., Li, N., Karck, M., et al. (2014). Cellular and molecular mechanisms of atrial arrhythmogenesis in patients with paroxysmal atrial fibrillation. Circulation 129, 145–156. doi: 10.1161/CIRCULATIONAHA.113.006641

PubMed Abstract | CrossRef Full Text | Google Scholar

Voigt, N., Li, N., Wang, Q., Wang, W., Trafford, A. W., Abu-Taha, I., et al. (2012). Enhanced sarcoplasmic reticulum Ca2+ leak and increased Na+ -Ca2+ exchanger function underlie delayed afterdepolarizations in patients with chronic atrial fibrillation. Circulation 125, 2059–2070. doi: 10.1161/CIRCULATIONAHA.111.067306

PubMed Abstract | CrossRef Full Text | Google Scholar

Voigt, N., Pearman, C. M., Dobrev, D., and Dibb, K. M. (2015). Methods for isolating atrial cells from large mammals and humans. J. Mol. Cell Cardiol. 86, 187–198. doi: 10.1016/j.yjmcc.2015.07.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, T. J., Larson, M. G., Levy, D., Vasan, R. S., Leip, E. P., Wolf, P. A., et al. (2003). Temporal relations of atrial fibrillation and congestive heart failure and their joint influence on mortality: the framingham heart study. Circulation 107, 2920–2925. doi: 10.1161/01.CIR.0000072767.89944.6E

PubMed Abstract | CrossRef Full Text | Google Scholar

Wehrens, X. H., Lehnart, S. E., Huang, F., Vest, J. A., Reiken, S. R., Mohler, P. J., et al. (2003). FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death. Cell 113, 829–840.

PubMed Abstract | Google Scholar

Wettwer, E., Hala, O., Christ, T., Heubach, J. F., Dobrev, D., Knaut, M., et al. (2004). Role of IKur in controlling action potential shape and contractility in the human atrium: influence of chronic atrial fibrillation. Circulation 110, 2299–2306. doi: 10.1161/01.CIR.0000145155.60288.71

PubMed Abstract | CrossRef Full Text | Google Scholar

Workman, A. J., Pau, D., Redpath, C. J., Marshall, G. E., Russell, J. A., Norrie, J., et al. (2009). Atrial cellular electrophysiological changes in patients with ventricular dysfunction may predispose to AF. Heart Rhythm 6, 445–451. doi: 10.1016/j.hrthm.2008.12.028

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, J., Cui, G., Esmailian, F., Plunkett, M., Marelli, D., Ardehali, A., et al. (2004). Atrial extracellular matrix remodeling and the maintenance of atrial fibrillation. Circulation 109, 363–368. doi: 10.1161/01.CIR.0000109495.02213.52

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamada, S., Lo, L. W., Chou, Y. H., Lin, W. L., Chang, S. L., Lin, Y. J., et al. (2017). Renal denervation regulates the atrial arrhythmogenic substrates through reverse structural remodeling in heart failure rabbit model. Int. J. Cardiol. 235, 105–113. doi: 10.1016/j.ijcard.2017.02.085

PubMed Abstract | CrossRef Full Text | Google Scholar

Yeh, Y. H., Wakili, R., Qi, X. Y., Chartier, D., Boknik, P., Kaab, S., et al. (2008). Calcium-handling abnormalities underlying atrial arrhythmogenesis and contractile dysfunction in dogs with congestive heart failure. Circ. Arrhythm. Electrophysiol. 1, 93–102. doi: 10.1161/CIRCEP.107.754788

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: atrial fibrillation, heart failure, heart failure with reduced ejection fraction, human atrial cardiomyocytes, Ca2+ handling

Citation: Molina CE, Abu-Taha IH, Wang Q, Roselló-Díez E, Kamler M, Nattel S, Ravens U, Wehrens XHT, Hove-Madsen L, Heijman J and Dobrev D (2018) Profibrotic, Electrical, and Calcium-Handling Remodeling of the Atria in Heart Failure Patients With and Without Atrial Fibrillation. Front. Physiol. 9:1383. doi: 10.3389/fphys.2018.01383

Received: 12 June 2018; Accepted: 11 September 2018;
Published: 09 October 2018.

Edited by:

Elisabetta Cerbai, Università degli Studi di Firenze, Italy

Reviewed by:

Stefan Dhein, Leipzig University, Germany
Cecilia Ferrantini, Università degli Studi di Firenze, Italy

Copyright © 2018 Molina, Abu-Taha, Wang, Roselló-Díez, Kamler, Nattel, Ravens, Wehrens, Hove-Madsen, Heijman and Dobrev. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Dobromir Dobrev,

These authors have contributed equally to this work