Nanoscale organization of ryanodine receptor distribution and phosphorylation pattern determines the dynamics of calcium sparks

被引:5
作者
Mesa, Maria Hernandez [1 ]
van den Brink, Jonas [1 ]
Louch, William E. [2 ,3 ,4 ]
McCabe, Kimberly J. [1 ]
Rangamani, Padmini [5 ]
机构
[1] Simula Res Lab, Dept Computat Physiol, Oslo, Norway
[2] Oslo Univ Hosp, Inst Expt Med Res, Oslo, Norway
[3] Univ Oslo, Oslo, Norway
[4] Univ Oslo, KG Jebsen Ctr Cardiac Res, Oslo, Norway
[5] Univ Calif San Diego, Dept Mech & Aerosp Engn, La Jolla, CA 92093 USA
关键词
KINASE-A PHOSPHORYLATION; CA2+ RELEASE; MODEL; CARDIOMYOCYTES; FKBP12.6; CAMKII;
D O I
10.1371/journal.pcbi.1010126
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Super-resolution imaging techniques have provided a better understanding of the relationship between the nanoscale organization and function of ryanodine receptors (RyRs) in cardiomyocytes. Recent data have indicated that this relationship is disrupted in heart failure (HF), as RyRs are dispersed into smaller and more numerous clusters. However, RyRs are also hyperphosphorylated in this condition, and this is reported to occur preferentially within the cluster centre. Thus, the combined impact of RyR relocalization and sensitization on Ca2+ spark generation in failing cardiomyocytes is likely complex and these observations suggest that both the nanoscale organization of RyRs and the pattern of phosphorylated RyRs within clusters could be critical determinants of Ca2+ spark dynamics. To test this hypothesis, we used computational modeling to quantify the relationships between RyR cluster geometry, phosphorylation patterns, and sarcoplasmic reticulum (SR) Ca2+ release. We found that RyR cluster disruption results in a decrease in spark fidelity and longer sparks with a lower amplitude. Phosphorylation of some RyRs within the cluster can play a compensatory role, recovering healthy spark dynamics. Interestingly, our model predicts that such compensation is critically dependent on the phosphorylation pattern, as phosphorylation localized within the cluster center resulted in longer Ca2+ sparks and higher spark fidelity compared to a uniformly distributed phosphorylation pattern. Our results strongly suggest that both the phosphorylation pattern and nanoscale RyR reorganization are critical determinants of Ca2+ dynamics in HF. Author summary Ryanodine receptors (RyRs) are ion channels located on the membrane of the sarcoplasmic reticulum that are responsible for an increase in cytosolic Ca2+ during cell excitation. Here, we investigate how the geometry of RyR clusters combined with spatial phosphorylation patterns impacts on Ca2+ spark generation and kinetics. The findings from our study show that phosphorylation pattern and both RyR cluster shape and dispersion have implications on Ca2+ spark activity and provide insights into altered Ca2+ dynamics during HF.
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页数:22
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共 31 条
[1]   Cardiac ryanodine receptor distribution is dynamic and changed by auxiliary proteins and post-translational modification [J].
Asghari, Parisa ;
Scriven, David R. L. ;
Ng, Myles ;
Panwar, Pankaj ;
Chou, Keng C. ;
van Petegem, Filip ;
Moore, Edwin D. W. .
ELIFE, 2020, 9
[2]   Optical single-channel resolution imaging of the ryanodine receptor distribution in rat cardiac myocytes [J].
Baddeley, David ;
Jayasinghe, Isuru D. ;
Lam, Leo ;
Rossberger, Sabrina ;
Cannell, Mark B. ;
Soeller, Christian .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (52) :22275-22280
[3]   Cardiac excitation-contraction coupling [J].
Bers, DM .
NATURE, 2002, 415 (6868) :198-205
[4]   Ryanodine Receptor S2808 Phosphorylation in Heart Failure Smoking Gun or Red Herring [J].
Bers, Donald M. .
CIRCULATION RESEARCH, 2012, 110 (06) :796-799
[5]   Interval estimation for a binomial proportion - Comment - Rejoinder [J].
Brown, LD ;
Cai, TT ;
DasGupta, A ;
Agresti, A ;
Coull, BA ;
Casella, G ;
Corcoran, C ;
Mehta, C ;
Ghosh, M ;
Santner, TJ ;
Brown, LD ;
Cai, TT ;
DasGupta, A .
STATISTICAL SCIENCE, 2001, 16 (02) :101-133
[6]   Control of Sarcoplasmic Reticulum Ca2+ Release by Stochastic RyR Gating within a 3D Model of the Cardiac Dyad and Importance of Induction Decay for CICR Termination [J].
Cannell, M. B. ;
Kong, C. H. T. ;
Imtiaz, M. S. ;
Laver, D. R. .
BIOPHYSICAL JOURNAL, 2013, 104 (10) :2149-2159
[7]   Ca2+/calmodulin-dependent protein kinase II phosphorylation of ryanodine receptor does affect calcium sparks in mouse ventricular myocytes [J].
Guo, Tao ;
Zhang, Tong ;
Mestril, Ruben ;
Bers, Donald M. .
CIRCULATION RESEARCH, 2006, 99 (04) :398-406
[8]   Kinetics of FKBP12.6 Binding to Ryanodine Receptors in Permeabilized Cardiac Myocytes and Effects on Ca Sparks [J].
Guo, Tao ;
Cornea, Razvan L. ;
Huke, Sabine ;
Camors, Emmanuel ;
Yang, Yi ;
Picht, Eckard ;
Fruen, Bradley R. ;
Bers, Donald M. .
CIRCULATION RESEARCH, 2010, 106 (11) :1743-U163
[9]   Modelling cardiac calcium sparks in a three-dimensional reconstruction of a calcium release unit [J].
Hake, Johan ;
Edwards, Andrew G. ;
Yu, Zeyun ;
Kekenes-Huskey, Peter M. ;
Michailova, Anushka P. ;
McCammon, J. Andrew ;
Holst, Michael J. ;
Hoshijima, Masahiko ;
McCulloch, Andrew D. .
JOURNAL OF PHYSIOLOGY-LONDON, 2012, 590 (18) :4403-4422
[10]   Local control of β-adrenergic stimulation: Effects on ventricular myocyte electrophysiology and Ca2+-transient [J].
Heijman, Jordi ;
Volders, Paul G. A. ;
Westra, Ronald L. ;
Rudy, Yoram .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2011, 50 (05) :863-871