Role of creatine kinase in cardiac excitation‐contraction coupling: studies in creatine kinase‐deficient mice

2002 ◽  
Vol 16 (7) ◽  
pp. 653-660 ◽  
Author(s):  
Bertrand Crozatier ◽  
Thierry Badoual ◽  
Ernest Boehm ◽  
Pierre‐Vladimir Ennezat ◽  
Thierry Guenoun ◽  
...  
Keyword(s):  
Creatine Kinase ◽  
Excitation Contraction Coupling ◽  
Contraction Coupling ◽  
Cardiac Excitation ◽  
Deficient Mice

Cardiac excitation-contraction coupling: role of membrane potential in regulation of contraction

2001 ◽  
Vol 280 (5) ◽  
pp. H1928-H1944 ◽  
Author(s):  
Gregory R. Ferrier ◽  
Susan E. Howlett
Keyword(s):  
Membrane Potential ◽  
Regulatory Mechanism ◽  
Cardiac Contraction ◽  
Release Mechanism ◽  
Excitation Contraction Coupling ◽  
Contraction Coupling ◽  
Regulation Of Contraction ◽  
Cardiac Excitation ◽  
The Impact

The steps that couple depolarization of the cardiac cell membrane to initiation of contraction remain controversial. Depolarization triggers a rise in intracellular free Ca2+ which activates contractile myofilaments. Most of this Ca2+ is released from the sarcoplasmic reticulum (SR). Two fundamentally different mechanisms have been proposed for SR Ca2+ release: Ca2+-induced Ca2+ release (CICR) and a voltage-sensitive release mechanism (VSRM). Both mechanisms operate in the same cell and may contribute to contraction. CICR couples the release of SR Ca2+ closely to the magnitude of the L-type Ca2+ current. In contrast, the VSRM is graded by membrane potential rather than Ca2+ current. The electrophysiological and pharmacological characteristics of the VSRM are strikingly different from CICR. Furthermore, the VSRM is strongly modulated by phosphorylation and provides a new regulatory mechanism for cardiac contraction. The VSRM is depressed in heart failure and may play an important role in contractile dysfunction. This review explores the operation and characteristics of the VSRM and CICR and discusses the impact of the VSRM on our understanding of cardiac excitation-contraction coupling.

scholarly journals Dual Role of Functionally Intact Dyadic Junctions in Cardiac Excitation-Contraction Coupling

2015 ◽  
Vol 108 (2) ◽  
pp. 266a
Author(s):  
Prakash Subramanyam ◽  
Donald D. Chang ◽  
Henry M. Colecraft
Keyword(s):  
Dual Role ◽  
Excitation Contraction Coupling ◽  
Contraction Coupling ◽  
Cardiac Excitation

scholarly journals SPEG: a key regulator of cardiac calcium homeostasis

2020 ◽  
Author(s):  
Hannah Campbell ◽  
Yuriana Aguilar-Sanchez ◽  
Ann P Quick ◽  
Dobromir Dobrev ◽  
Xander H T Wehrens
Keyword(s):  
Human Disease ◽  
Striated Muscle ◽  
Genetic Diseases ◽  
Cardiac Contractility ◽  
Tubule Formation ◽  
Excitation Contraction Coupling ◽  
Contraction Coupling ◽  
Membrane Complex ◽  
Cardiac Excitation

Abstract Proper cardiac Ca2+ homeostasis is essential for normal excitation–contraction coupling. Perturbations in cardiac Ca2+ handling through altered kinase activity has been implicated in altered cardiac contractility and arrhythmogenesis. Thus, a better understanding of cardiac Ca2+ handling regulation is vital for a better understanding of various human disease processes. ‘Striated muscle preferentially expressed protein kinase’ (SPEG) is a member of the myosin light chain kinase family that is key for normal cardiac function. Work within the last 5 years has revealed that SPEG has a crucial role in maintaining normal cardiac Ca2+ handling through maintenance of transverse tubule formation and phosphorylation of junctional membrane complex proteins. Additionally, SPEG has been causally impacted in human genetic diseases such as centronuclear myopathy and dilated cardiomyopathy as well as in common acquired cardiovascular disease such as heart failure and atrial fibrillation. Given the rapidly emerging role of SPEG as a key cardiac Ca2+ regulator, we here present this review in order to summarize recent findings regarding the mechanisms of SPEG regulation of cardiac excitation–contraction coupling in both physiology and human disease. A better understanding of the roles of SPEG will be important for a more complete comprehension of cardiac Ca2+ regulation in physiology and disease.

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