» Articles » PMID: 21943409

Dynamics of Calcium Sparks and Calcium Leak in the Heart

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2011 Sep 28
PMID 21943409
Citations 83
Authors
Affiliations
Soon will be listed here.
Abstract

We present what we believe to be a new mathematical model of Ca(2+) leak from the sarcoplasmic reticulum (SR) in the heart. To our knowledge, it is the first to incorporate a realistic number of Ca(2+)-release units, each containing a cluster of stochastically gating Ca(2+) channels (RyRs), whose biophysical properties (e.g., Ca(2+) sensitivity and allosteric interactions) are informed by the latest molecular investigations. This realistic model allows for the detailed characterization of RyR Ca(2+)-release properties, and shows how this balances reuptake by the SR Ca(2+) pump. Simulations reveal that SR Ca(2+) leak consists of brief but frequent single RyR openings (~3000 cell(-1) s(-1)) that are likely to be experimentally undetectable, and are, therefore, "invisible". We also observe that these single RyR openings can recruit additional RyRs to open, due to elevated local (Ca(2+)), and occasionally lead to the generation of Ca(2+) sparks (~130 cell(-1) s(-1)). Furthermore, this physiological formulation of "invisible" leak allows for the removal of the ad hoc, non-RyR mediated Ca(2+) leak terms present in prior models. Finally, our model shows how Ca(2+) sparks can be robustly triggered and terminated under both normal and pathological conditions. Together, these discoveries profoundly influence how we interpret and understand diverse experimental and clinical results from both normal and diseased hearts.

Citing Articles

Blink nadir measurements of sarcoplasmic reticulum are consistent with strong local Ca depletion.

Gillespie D Biophys J. 2024; 124(2):245-255.

PMID: 39604260 PMC: 11788478. DOI: 10.1016/j.bpj.2024.11.3316.


Using a Failing Human Ventricular Cardiomyocyte Model to Re-Evaluate Ca Cycling, Voltage Dependence, and Spark Characteristics.

Alvarez J, Jafri M, Ullah A Biomolecules. 2024; 14(11).

PMID: 39595549 PMC: 11591732. DOI: 10.3390/biom14111371.


Gain-of-Function and Loss-of-Function Mutations in the RyR2-Expressing Gene Are Responsible for the CPVT1-Related Arrhythmogenic Activities in the Heart.

Paudel R, Jafri M, Ullah A Curr Issues Mol Biol. 2024; 46(11):12886-12910.

PMID: 39590361 PMC: 11592891. DOI: 10.3390/cimb46110767.


Structure, Function, and Regulation of the Junctophilin Family.

Hall D, Takeshima H, Song L Annu Rev Physiol. 2023; 86:123-147.

PMID: 37931168 PMC: 10922073. DOI: 10.1146/annurev-physiol-042022-014926.


Elementary intracellular Ca signals approximated as a transition of release channel system from a metastable state.

Veron G, Maltsev V, Stern M, Maltsev A J Appl Phys. 2023; 134(12):124701.

PMID: 37744735 PMC: 10517864. DOI: 10.1063/5.0151255.


References
1.
Groff J, Smith G . Ryanodine receptor allosteric coupling and the dynamics of calcium sparks. Biophys J. 2008; 95(1):135-54. PMC: 2426658. DOI: 10.1529/biophysj.107.119982. View

2.
Wehrens X, Lehnart S, Huang F, Vest J, Reiken S, Mohler P . FKBP12.6 deficiency and defective calcium release channel (ryanodine receptor) function linked to exercise-induced sudden cardiac death. Cell. 2003; 113(7):829-40. DOI: 10.1016/s0092-8674(03)00434-3. View

3.
Williams G, Huertas M, Sobie E, Jafri M, Smith G . Moment closure for local control models of calcium-induced calcium release in cardiac myocytes. Biophys J. 2008; 95(4):1689-703. PMC: 2483752. DOI: 10.1529/biophysj.107.125948. View

4.
Zima A, Bovo E, Bers D, Blatter L . Ca²+ spark-dependent and -independent sarcoplasmic reticulum Ca²+ leak in normal and failing rabbit ventricular myocytes. J Physiol. 2010; 588(Pt 23):4743-57. PMC: 3010143. DOI: 10.1113/jphysiol.2010.197913. View

5.
Qin J, Valle G, Nani A, Nori A, Rizzi N, Priori S . Luminal Ca2+ regulation of single cardiac ryanodine receptors: insights provided by calsequestrin and its mutants. J Gen Physiol. 2008; 131(4):325-34. PMC: 2279168. DOI: 10.1085/jgp.200709907. View