Calcium and Excitation-Contraction Coupling in the Heart.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 28684623.
- Also identified by DOI 10.1161/CIRCRESAHA.117.310230 and PMC identifier 5497788.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Cardiac contractility is regulated by changes in intracellular Ca concentration ([Ca<sup>2+</sup>]<sub>i</sub>). Normal function requires that [Ca<sup>2+</sup>]<sub>i</sub> be sufficiently high in systole and low in diastole. Much of the Ca needed for contraction comes from the sarcoplasmic reticulum and is released by the process of calcium-induced calcium release. The factors that regulate and fine-tune the initiation and termination of release are reviewed. The precise control of intracellular Ca cycling depends on the relationships between the various channels and pumps that are involved. We consider 2 aspects: (1) structural coupling: the transporters are organized within the dyad, linking the transverse tubule and sarcoplasmic reticulum and ensuring close proximity of Ca entry to sites of release. (2) Functional coupling: where the fluxes across all membranes must be balanced such that, in the steady state, Ca influx equals Ca efflux on every beat. The remainder of the review considers specific aspects of Ca signaling, including the role of Ca buffers, mitochondria, Ca leak, and regulation of diastolic [Ca<sup>2+</sup>]<sub>i</sub>.
Medical subject headings
- Calcium
- Calcium Signaling
- Excitation Contraction Coupling
- Mitochondria, Heart
- Myocytes, Cardiac