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Late Ca2+ Sparks and Ripples During the Systolic Ca2+ Transient in Heart Muscle Cells

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)473-478
Number of pages5
JournalCirculation Research
Volume122
Early online date27 Dec 2017
DOIs
DateAccepted/In press - 24 Dec 2017
DateE-pub ahead of print - 27 Dec 2017
DatePublished (current) - 2018

Abstract

Rationale: The development of a refractory period for Ca2+ spark initiation after Ca2+ release in cardiac myocytes, should inhibit further Ca2+ release during the action potential (AP) plateau. However, Ca2+
release sites that did not initially activate, or which have prematurely recovered from refractoriness might release Ca2+ later during the AP and alter the cell-wide Ca2+ transient.
Objective: To investigate the possibility of late Ca2+ spark (LCS) activity in intact isolated cardiac myocytes using fast confocal line scanning with improved confocality and signal to noise.
Methods and Results: We recorded Ca2+ transients from cardiac ventricular myocytes isolated from rabbit hearts. APs were produced by electrical stimulation and rapid solution changes were used to modify the Ltype Ca2+ current. After the upstroke of the Ca2+ transient, late Ca2+ sparks (LCS) were detected which had increased amplitude compared to diastolic Ca2+ sparks. LCS are triggered by both L-type Ca2+ channel activity during the action potential plateau, as well as by the increase of cytosolic Ca2+ associated with the Ca2+ transient itself. Importantly, a mismatch between SR load and L-type Ca2+ trigger can increase the number of LCS. The likelihood of triggering a LCS also depends on recovery from refractoriness that appears after prior activation. Consequences of LCS include a reduced rate of decline of the Ca2+ transient and, if frequent, formation of microscopic propagating Ca2+ release events (Ca2+ ripples). Ca2+ ripples resemble Ca2+ waves in terms of local propagation velocity but spread for only a short distance due to limited regeneration.
Conclusions: These new types of Ca2+ signalling behaviour extend our understanding of Ca2+ mediated signalling. LCS may provide an arrhythmogenic substrate by slowing the Ca2+ transient decline as well as by amplifying maintained Ca2+ current effects on intracellular Ca2+ and consequently Na+/Ca2+ exchange current.

Additional information

epub 24 December 2017

    Research areas

  • Heart, Ca2+ sparks, excitation-contraction coupling, cytosolic Ca2+, calcium signaling, cardiomyocyte, cardiac myocyte

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via AHA at https://doi.org/10.1161/CIRCRESAHA.117.312257 . Please refer to any applicable terms of use of the publisher.

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