The ryanodine receptor microdomain in cardiomyocytes

被引:2
|
作者
Dries, Eef [1 ,3 ]
Gilbert, Guillaume [1 ,2 ]
Roderick, H. Llewelyn [1 ]
Sipido, Karin R. [1 ]
机构
[1] Katholieke Univ Leuven, Dept Cardiovasc Sci, Lab Expt Cardiol, Leuven, Belgium
[2] Univ Brest, Lab ORPHY EA 4324, Brest, France
[3] Katholieke Univ Leuven, Dept Cardiovasc Sci, Lab Expt Cardiol, Herestr 49 box 704, B-3000 Leuven, Belgium
关键词
Cardiomyocyte; Ryanodine receptor; Microdomains; Calcium; RyR Clusters; Local signaling; PROTEIN-KINASE-II; RETICULUM CA2+ RELEASE; HUMAN HEART-FAILURE; T-TUBULE MEMBRANE; SARCOPLASMIC-RETICULUM; CALCIUM-RELEASE; CA2+-RELEASE CHANNEL; PHOSPHORYLATION SITE; REDUCED SYNCHRONY; REDOX REGULATION;
D O I
10.1016/j.ceca.2023.102769
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ryanodine receptor type 2 (RyR) is a key player in Ca2+ handling during excitation-contraction coupling. During each heartbeat, RyR channels are responsible for linking the action potential with the contractile machinery of the cardiomyocyte by releasing Ca2+ from the sarcoplasmic reticulum. RyR function is fine-tuned by associated signalling molecules, arrangement in clusters and subcellular localization. These parameters together define RyR function within microdomains and are subject to disease remodelling. This review describes the latest findings on RyR microdomain organization, the alterations with disease which result in increased subcellular heterogeneity and emergence of microdomains with enhanced arrhythmogenic potential, and presents novel technologies that guide future research to study and target RyR channels within specific microdomains.
引用
收藏
页数:15
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