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Synchrony of cardiomyocyte Ca(2+) release is controlled by T-tubule organization, SR Ca(2+) content, and ryanodine receptor Ca(2+) sensitivity.
- Source :
-
Biophysical journal [Biophys J] 2013 Apr 16; Vol. 104 (8), pp. 1685-97. - Publication Year :
- 2013
-
Abstract
- Recent work has demonstrated that cardiomyocyte Ca(2+)release is desynchronized in several pathological conditions. Loss of Ca(2+) release synchrony has been attributed to t-tubule disruption, but it is unknown if other factors also contribute. We investigated this issue in normal and failing myocytes by integrating experimental data with a mathematical model describing spatiotemporal dynamics of Ca(2+) in the cytosol and sarcoplasmic reticulum (SR). Heart failure development in postinfarction mice was associated with progressive t-tubule disorganization, as quantified by fast-Fourier transforms. Data from fast-Fourier transforms were then incorporated in the model as a dyadic organization index, reflecting the proportion of ryanodine receptors located in dyads. With decreasing dyadic-organization index, the model predicted greater dyssynchrony of Ca(2+) release, which exceeded that observed in experimental line-scan images. Model and experiment were reconciled by reducing the threshold for Ca(2+) release in the model, suggesting that increased RyR sensitivity partially offsets the desynchronizing effects of t-tubule disruption in heart failure. Reducing the magnitude of SR Ca(2+) content and release, whether experimentally by thapsigargin treatment, or in the model, desynchronized the Ca(2+) transient. However, in cardiomyocytes isolated from SERCA2 knockout mice, RyR sensitization offset such effects. A similar interplay between RyR sensitivity and SR content was observed during treatment of myocytes with low-dose caffeine. Initial synchronization of Ca(2+) release during caffeine was reversed as SR content declined due to enhanced RyR leak. Thus, synchrony of cardiomyocyte Ca(2+) release is not only determined by t-tubule organization but also by the interplay between RyR sensitivity and SR Ca(2+) content.<br /> (Copyright © 2013 Biophysical Society. Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Caffeine pharmacology
Calcium Channel Blockers pharmacology
Cytosol metabolism
Female
Mice
Mice, Inbred C57BL
Mice, Knockout
Models, Biological
Myocardial Infarction metabolism
Myocardial Infarction pathology
Myocytes, Cardiac ultrastructure
Ryanodine Receptor Calcium Release Channel drug effects
Sarcolemma metabolism
Sarcoplasmic Reticulum Calcium-Transporting ATPases genetics
Sarcoplasmic Reticulum Calcium-Transporting ATPases metabolism
Thapsigargin pharmacology
Calcium metabolism
Calcium Signaling
Myocytes, Cardiac metabolism
Ryanodine Receptor Calcium Release Channel metabolism
Sarcolemma ultrastructure
Sarcoplasmic Reticulum metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1542-0086
- Volume :
- 104
- Issue :
- 8
- Database :
- MEDLINE
- Journal :
- Biophysical journal
- Publication Type :
- Academic Journal
- Accession number :
- 23601316
- Full Text :
- https://doi.org/10.1016/j.bpj.2013.03.022