Region-specific distribution of transversal-axial tubule system organization underlies heterogeneity of calcium dynamics in the right atrium
The atrial myocardium demonstrates the highly heterogeneous organization of the transversal-axial tubule system (TATS), while its anatomical distribution and region-specific impact on Ca2+ dynamics remain unknown. We developed a novel method for high-resolution confocal imaging of TATS in intact live mouse atrial myocardium and applied a Matlab-based computational algorithm for the automated analysis of TATS integrity. We observed a 2-fold higher (P<0.01) TATS density in the right atrial appendage (RAA) than in the inter-caval region (ICR, the anatomical region between the superior vena cava and atrioventricular junction and between the crista terminalis and inter-atrial septum). While RAA predominantly consisted of well-tubulated myocytes, ICR showed partially tubulated/untubulated cells. Similar TATS distribution was also observed in healthy human atrial myocardium sections. In both mouse atrial preparations and isolated mouse atrial myocytes, we observed a strong anatomical correlation between TATS distribution and Ca2+ transient synchronization and rise-up time. This region-specific difference in Ca2+ transient morphology disappeared after formamide-induced detubulation. ICR myocytes showed a prolonged action potential duration at 80% of repolarization as well as a significantly lower expression of RyR2 and Cav1.2 proteins, but similar levels of NCX1 and Cav1.3 compared to RAA tissue. Our findings provide a detailed characterization of the region-specific distribution of TATS in mouse and human atrial myocardium highlighting the structural foundation for anatomical heterogeneity of Ca2+ dynamics and contractility in the atria. These results could indicate different roles of TATS in Ca2+ signaling at distinct anatomical regions of the atria and provide mechanistic insight into pathological atrial remodeling.