Arrhythmia initiation in catecholaminergic polymorphic ventricular tachycardia type 1 depends on both heart rate and sympathetic stimulation

Fig 1. Bicycle stress testing showed the heart rate-dependence of arrhythmias in patients with CPVT1, while atrial pacing did not induce arrhythmias. (A) ECG tracings from a patient with CPVT1 recorded during a bicycle stress test. RR-interval was measured before PVCs occurred. (B) Bar graphs of RR-intervals of sinus beats in stable sinus rhythm (baseline), and immediately before the occurrence of isolated PVCs, PVCs in bigeminy, and couplets or nsVT, respectively. Data from 31 bicycle stress tests performed by 16 patients with CPVT1. *p<0.05 compared to baseline with one-way ANOVA with Bonferroni correction. (C) Individual plots of RR-intervals of patients who developed arrhythmias during the stress test. RR-intervals at baseline and before the first arrhythmic event are shown, both in absence and in presence of βAR antagonists. (D) ECG tracings from a patient with CPVT1 recorded during a bicycle stress test (upper panel) with PVCs in bigeminy at 120 beat per minute (b.p.m.), and at rest during pacing through an atrial lead with no PVCs at 130 b.p.m. (lower panel).

Fig 2. High pacing frequency induced Ca2+ waves in RyR2-RS mouse left ventricular cardiomyocytes, but βAR stimulation was necessary to reveal increased propensity compared to WT. (A) Tracings of whole-cell Ca2+ fluorescence showing Ca2+ transients and Ca2+ waves (arrow) during 0.5 Hz pacing by field stimulation in absence and presence of stimulation of βARs with ISO. (B) Bar graphs showing the mean frequency of Ca2+ waves in RyR2-RS and WT cardiomyocytes in a 10 s post-pacing period after 0.5, 4 and 8 Hz pacing in absence and presence of ISO, respectively. Analyzed by Nested ANOVA with data from 9 RyR2-RS and 8–15 WT mice per bar (29–55 cells per result). (C) Bar graphs showing the mean Ca2+ wave latency in RyR2-RS and WT cardiomyocytes after different pacing frequencies, in absence and presence of ISO. Analyzed by Nested ANOVA with data from 9–16 RyR2-RS and 10–21 WT mice per bar (28–70 cells per result). (D) Bar graph showing the mean frequency of Ca2+ waves in a 10 s period after 4 Hz pacing in 0, 2, 20 and 200 nM ISO. Analyzed by Nested ANOVA with data from 3–13 RyR2-RS and 3–18 WT mice (8–65 cells per result). *p<0.05 RyR2-RS vs WT, #p<0.05 vs 0.5 Hz in the same conditions (+/-…

Fig 3. High pacing frequency induced Ca2+ sparks in RyR2-RS mouse left ventricular cardiomyocytes, but βARstimulation was necessary to reveal increased propensity compared to WT. (A) Line scan confocal imaging in absence of stimulation of βARs with ISO after 0.5 Hz pacing in WT (upper panel) and RyR2-RS (lower panel). (B) Line scan confocal imaging in presence of ISO after 0.5 Hz pacing in WT (upper panel) and RyR2-RS (lower panel). (C) and (D) Density plots illustrating the distribution of number of cells with 0–5 Ca2+ sparks per 100 μm per second, occurring after 0.5, 4 and 8 Hz pacing in absence and presence of ISO, respectively. Higher density means more cells. The legend shows how different patterns represent WT or RyR2-RS, respectively. Results from Poisson analysis of data from 13 RyR2-RS mice (47 cells) and 15 WT mice (62 cells), *p<0.05.

Fig 4. Ca2+ handling characteristics in RyR2-RS left ventricular cardiomyocytes indicated increased RyR open probability and lower threshold for diastolic Ca2+ release. (A) A whole-cell Ca2+ fluorescence tracing showing the experimental protocol with 0.5, 4 and 8 Hz pacing at baseline and during βAR stimulation. (B) Tracings of whole-cell Ca2+ fluorescence showing Ca2+ transients during 0.5 Hz pacing in absence and presence of ISO. (C) Tracings of whole-cell Ca2+ fluorescence showing caffeine-elicited Ca2+ release after 0.5 Hz pacing. Peak fluorescence intensity was used for measurements of SR Ca2+ content. Caffeine was added immediately after the last stimulated Ca2+ transient. (D) Tracings of whole-cell Ca2+ fluorescence showing caffeine-elicited Ca2+ release at the time of occurrence of Ca2+ waves after 4 Hz stimulation. Caffeine was added immediately after the occurrence of a Ca2+ wave. This protocol was used for measurements of threshold SR Ca2+ content. Peak fluorescence intensity was used for measurements of SR Ca2+ content. (E) Bar graphs showing mean Ca2+ transient amplitude at different pacing frequencies in absence and presence of ISO. Analyzed by Nested ANOVA with data from…

Fig 5. Analysis of key phosphoproteins did not show any differences between RyR2-RS and WT. Protein abundance was analyzed after 4 and 8 Hz pacing in absence and presence of ISO. (A) CaMKII phospho-threonine286 (pCaMKII), (B) RyR2 phospho-serine-2808 (pRyR2808), (C) RyR2 phospho-serine-2814 (pRyR 2814), (D) PLB phospho-serine 16 (pPLB-Ser16), (E) PLB phospho-threonine 17 (pPLB-Thr17), (F) SERCA2a. The graphs show mean protein abundance in 6 hearts from each group. Western blot results were normalized to WT (in the absence of ISO stimulation) at 4 and 8 Hz. *p<0.05, #p<0.05 vs. baseline in absence of ISO with Student`s T-test for unpaired data.

Fig 6. Computational modelling elucidated the interaction between pacing frequency and βAR stimulation in Ca2+ wave development. (A) Modelled representation of whole-cell intracellular Ca2+ ([Ca2+]i) and SR Ca2+ content ([Ca2+]SR), as well as fluctuations in the level of RyR2 phosphorylation (pRyR) relative to a quiescent myocyte, in a 10 s period after pacing at 0.5 Hz in absence (left panel) and presence of ISO (right panel). Similar simulations were performed with 4 Hz pacing (not shown). The impact of CaMKII and phosphorylation of RyR2 was tested by omitting CaMKII from the model entirely (÷CaMKII), and by holding RyR2 phosphorylation to a set level found in quiescent cells in absence of ISO (RyR P-clamp). (B) SR Ca2+ content ([Ca2+]SR), level of RyR2 phosphorylation (pRyR), and abundance of autophosphorylated CaMKII (pCaMKII) at the time of occurrence of the first Ca2+ wave after 0.5 and 4 Hz pacing in absence and presence of ISO. Note that after 0.5 Hz in absence of ISO no Ca2+ waves occurred in WT. (C) SR Ca2+ content, level of RyR2 phosphorylation (RyR-P), and CaMKII activity at the time of the first and subsequent Ca2+ waves in a 10 s period after 4 Hz pacing.