β-Adrenergic receptor signaling in the heart: Role of CaMKII

被引:178
作者
Grimm, Michael [1 ]
Brown, Joan Heller [1 ]
机构
[1] Univ Calif San Diego, Dept Pharmacol, San Diego, CA 92103 USA
关键词
CaMKII; Beta-adrenergic receptor signaling; Excitation-contraction coupling; Heart failure; Hypertrophy; Apoptosis; Arrhythmia; CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE; CARDIAC RYANODINE RECEPTOR; CALCIUM-RELEASE CHANNEL; THR(17) PHOSPHOLAMBAN PHOSPHORYLATION; FREQUENCY-DEPENDENT ACCELERATION; NODE PACEMAKER ACTIVITY; RETICULUM CA2+ RELEASE; II INHIBITION PROTECTS; INTACT BEATING HEARTS; SARCOPLASMIC-RETICULUM;
D O I
10.1016/j.yjmcc.2009.10.016
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The multi functional Ca2+/calmodulin-dependent protein kinase II (CaMKII) targets a number of Ca2+ homeostatic proteins and regulates gene transcription. Many of the substrates phosphorylated by CaMKII are also substrates for protein kinase A (PKA), the best known downstream effector of beta-adrenergic receptor (beta-AR) signaling. While PKA and CaMKII are conventionally considered to transduce signals through separate pathways, there is a body of evidence suggesting that CaMKII is activated in response to beta-AR stimulation and that some of the downstream effects of beta-AR Stimulation are actually mediated by CaMKII. The signaling pathway through which beta-AR stimulation activates CaMKII, in parallel with or downstream of PKA, is not well-defined. This review considers the evidence for and mechanisms by which CaMKII is activated in response to beta-AR stimulation. In addition the potential role of CaMKII in beta-AR regulation of cardiac function is considered. Notably, although many CaMKII targets (e.g., phospholamban or the ryanodine receptor) are central to the regulation of Ca2+ handling, and effects of CaMKII on Ca2+ handling are detectable, inhibition or gene deletion of CaMKII has relatively little effect on the acute physiological contractile response to beta-AR. On the other hand CaMKII expression and activity are increased in heart failure, a pathophysiological condition characterized by chronic stimulation of cardiac beta-ARs. Blockade of beta-ARs is an accepted therapy for treatment of chronic heart failure although the rationale for its beneficial effects in cardiomyocytes is uncertain. There is growing evidence that inhibition or gene deletion of CaMKII also has a significant beneficial impact on the development of heart failure. The possibility that excessive beta-AR stimulation is detrimental because of its effects on CaMKII mediated Ca2+ handling disturbances (e.g., ryanodine receptor phosphorylation and diastolic SR Ca2+ leak) is an intriguing hypothesis that merits future consideration. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:322 / 330
页数:9
相关论文
共 127 条
[1]   Ca2+/calmodulin-dependent protein kinase modulates cardiac ryanodine receptor phosphorylation and sarcoplasmic reticulum Ca2+ leak in heart failure [J].
Ai, X ;
Curran, JW ;
Shannon, TR ;
Bers, DM ;
Pogwizd, SM .
CIRCULATION RESEARCH, 2005, 97 (12) :1314-1322
[2]   MULTIFUNCTIONAL CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE MEDIATES CA2+-INDUCED ENHANCEMENT OF THE L-TYPE CA2+ CURRENT IN RABBIT VENTRICULAR MYOCYTES [J].
ANDERSON, ME ;
BRAUN, AP ;
SCHULMAN, H ;
PREMACK, BA .
CIRCULATION RESEARCH, 1994, 75 (05) :854-861
[3]   Histone deacetylase 5 acquires calcium/calmodulin-dependent kinase II responsiveness by oligomerization with histone deacetylase 4 [J].
Backs, Johannes ;
Backs, Thea ;
Bezprozvannaya, Svetlana ;
McKinsey, Timothy A. ;
Olson, Eric N. .
MOLECULAR AND CELLULAR BIOLOGY, 2008, 28 (10) :3437-3445
[4]   CaM kinase II selectively signals to histone deacetylase 4 during cardiornyocyte hypertrophy [J].
Backs, Johannes ;
Song, Kunhua ;
Bezprozvannaya, Svetlana ;
Chang, Shurong ;
Olson, Eric N. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (07) :1853-1864
[5]   The endogenous cardiac sarcoplasmic reticulum Ca2+/calmodulin-dependent kinase is activated in response to beta-adrenergic stimulation and becomes Ca2+-independent in intact beating hearts [J].
Baltas, LG ;
Karczewski, P ;
Bartel, S ;
Krause, EG .
FEBS LETTERS, 1997, 409 (02) :131-136
[6]   Phosphorylation of phospholamban at threonine-17 in the absence and presence of β-adrenergic stimulation in neonatal rat cardiomyocytes [J].
Bartel, S ;
Vetter, D ;
Schlegel, WP ;
Wallukat, G ;
Krause, EG ;
Karczewski, P .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2000, 32 (12) :2173-2185
[7]   Intact β-adrenergic response and unmodified progression toward heart failure in mice with genetic ablation of a major protein kinase a phosphorylation site in the cardiac ryanodine receptor [J].
Benkusky, Nancy A. ;
Weber, Craig S. ;
Scherman, Joseph A. ;
Farrell, Emily F. ;
Hacker, Timothy A. ;
John, Manorama C. ;
Powers, Patricia A. ;
Valdivia, Hector H. .
CIRCULATION RESEARCH, 2007, 101 (08) :819-829
[8]   Ca2+/Calmodulin-Dependent protein kinase IIδ and protein kinase D overexpression reinforce the histone deacetylase 5 redistribution in heart failure [J].
Bossuyt, Julie ;
Helmstadter, Kathryn ;
Wu, Xu ;
Clements-Jewery, Hugh ;
Haworth, Robert S. ;
Avkiran, Metin ;
Martin, Jody L. ;
Pogwizd, Steven M. ;
Bers, Donald M. .
CIRCULATION RESEARCH, 2008, 102 (06) :695-702
[9]   An ultrasensitive Ca2+/calmodulin-dependent protein kinase II-protein phosphatase 1 switch facilitates specificity in postsynaptic calcium signaling [J].
Bradshaw, JM ;
Kubota, Y ;
Meyer, T ;
Schulman, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (18) :10512-10517
[10]   A-kinase Anchoring Proteins: From Protein Complexes to Physiology and Disease [J].
Carnegie, Graeme K. ;
Means, Christopher K. ;
Scott, John D. .
IUBMB LIFE, 2009, 61 (04) :394-406