Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/32704
Title: Intracellular zinc modulates cardiac ryanodine receptor-mediated calcium release.
Authors: Woodier, J.
Rainbow, Richard D.
Stewart, A. J.
Pitt, S. J.
First Published: 3-Jun-2015
Publisher: American Society for Biochemistry and Molecular Biology
Citation: The Journal of Biological Chemistry, Vol. 290, No. 28, pp. 17599 –17610, July 10, 2015
Abstract: Aberrant Zn(2+)-homeostasis is a hallmark of certain cardiomyopathies associated with altered contractile force. In this study we addressed whether Zn(2+) modulates cardiac ryanodine receptor gating and Ca(2+)-dynamics in isolated cardiomyocytes. We reveal that Zn(2+) is a high affinity regulator of RyR2 displaying three modes of operation. Picomolar free Zn(2+) concentrations potentiate RyR2 responses but channel activation is still dependent on the presence of cytosolic Ca(2+). At concentrations of free Zn(2+) >1 nM, Zn(2+) is the main activating ligand and the dependency on Ca(2+) is removed. Zn(2+) is therefore a higher affinity activator of RyR2 than Ca(2+). Millimolar levels of free Zn(2+) were found to inhibit channel openings. In cardiomyocytes, consistent with our single-channel results, we show that Zn(2+) modulates both the frequency and amplitude of Ca(2+) waves in a concentration dependent manner and that physiological levels of Zn(2+) elicit Ca(2+)-release in the absence of activating levels of cytosolic Ca(2+). This highlights a new role for intracellular Zn(2+) in shaping Ca(2+)-dynamics in cardiomyocytes through modulation of RyR2 gating.
DOI Link: 10.1074/jbc.M115.661280
ISSN: 0021-9258
eISSN: 1083-351X
Links: http://www.jbc.org/content/290/28/17599
http://hdl.handle.net/2381/32704
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: © 2015 by The American Society for Biochemistry and Molecular Biology, Inc. Final version free via Creative Commons CC-BY license.
Appears in Collections:Published Articles, Dept. of Cardiovascular Sciences

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