Why the study?
Does T-tubular electrical remodeling alter local calcium release in heart failure cardiomyocytes?
Does T-tubular electrical remodeling alter local calcium release in heart failure cardiomyocytes?
T-tubular electrical remodeling in heart failure leads to altered calcium release kinetics and spontaneous depolarizations, potentially contributing to contractile dysfunction and arrhythmias.
T-tubular uncoupling may drive local Ca dysregulation and arrhythmias in HF; hypothesis-generating for human validation and targeted therapies.
Action potentials (APs), via the transverse axial tubular system (TATS), synchronously trigger uniform Ca(2+) release throughout the cardiomyocyte. In heart failure (HF), TATS structural remodeling occurs, leading to asynchronous Ca(2+) release across the myocyte and contributing to contractile dysfunction. In cardiomyocytes from failing rat hearts, we previously documented the presence of TATS elements which failed to propagate AP and displayed spontaneous electrical activity; the consequence for Ca(2+) release remained, however, unsolved. Here, we develop an imaging method to simultaneously assess TATS electrical activity and local Ca(2+) release. In HF cardiomyocytes, sites where T-tubules fail to conduct AP show a slower and reduced local Ca(2+) transient compared with regions with electrically coupled elements. It is concluded that TATS electrical remodeling is a major determinant of altered kinetics, amplitude, and homogeneity of Ca(2+) release in HF. Moreover, spontaneous depolarization events occurring in failing T-tubules can trigger local Ca(2+) release, resulting in Ca(2+) sparks. The occurrence of tubule-driven depolarizations and Ca(2+) sparks may contribute to the arrhythmic burden in heart failure.
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Crocini et al. (2014) studied this question.
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