Why the study?
Recent work has revealed newfound appreciation of the plasticity of the t-tubule network, prompting a summary of its dynamic regulation and emerging therapeutic targets.
Cardiac t-tubules are dynamic structures essential for excitation-contraction coupling, and their plasticity in heart failure presents emerging targets for future therapies.
In mammalian cardiac myocytes, the plasma membrane includes the surface sarcolemma but also a network of membrane invaginations called transverse (t-) tubules. These structures carry the action potential deep into the cell interior, allowing efficient triggering of Ca 2+ release and initiation of contraction. Once thought to serve as rather static enablers of excitation-contraction coupling, recent work has provided a newfound appreciation of the plasticity of the t-tubule network's structure and function. Indeed, t-tubules are now understood to support dynamic regulation of the heartbeat across a range of timescales, during all stages of life, in both health and disease. This review article aims to summarize these concepts, with consideration given to emerging t-tubule regulators and their targeting in future therapies.
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Dibb et al. (2021) studied this question.
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