Sarcoplasmic reticulum Ca-ATPase-phospholamban interactions and dilated cardiomyopathy

被引:62
作者
Haghighi, K [1 ]
Gregory, KN [1 ]
Kranias, EG [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Pharmacol & Cell Biophys, Cincinnati, OH 45267 USA
关键词
phospholamban; null; overexpression; phosphorylation; sarcoplasmic reticulum Ca-ATPase; mutation; heart failure; dilated cardiomyopathy;
D O I
10.1016/j.bbrc.2004.07.164
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dilated cardiomyopathy is a disease of the heart muscle resulting from a diverse array of conditions that damages the heart and impairs myocardial function. Heart failure occurs when the heart is unable to pump blood at a rate which can accommodate the heart muscle's metabolic requirements. Several signaling pathways have been shown to be involved in the induction of cardiac disease and heart failure. Many of these pathways are linked to cardiac sarcoplasmic reticulum. (SR) Ca cycling directly or indirectly. A large body of evidence points to the central role of abnormal Ca handling by SR proteins, Ca-ATPase pump (SERCA2a) and phospholamban (PLN), in pathophysiological heart conditions, compromising the contractile state of the cardiomyocytes. This review summarizes studies which highlight the key role of these two SR proteins in the regulation of cardiac function, the significance of SERCA2a-PLN interactions using transgenic approaches, and the recent discoveries of human PLN mutations leading to disease states. Finally, we will discuss extrapolation of experimental paradigms generated in animal models to the human condition. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1214 / 1222
页数:9
相关论文
共 45 条
[1]   SARCOPLASMIC-RETICULUM GENE-EXPRESSION IN CARDIAC-HYPERTROPHY AND HEART-FAILURE [J].
ARAI, M ;
MATSUI, H ;
PERIASAMY, M .
CIRCULATION RESEARCH, 1994, 74 (04) :555-564
[2]   Transmembrane helix M6 in sarco(endo)plasmic reticulum Ca2+-ATPase forms a functional interaction site with phospholamban -: Evidence for physical, interactions at other sites [J].
Asahi, M ;
Kimura, Y ;
Kurzydlowski, R ;
Tada, M ;
MacLennan, DH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (46) :32855-32862
[3]   Phospholamban domain IB forms an interaction site with the loop between transmembrane helices M6 and M7 of sarco(endo)plasmic reticulum Ca2+ ATPases [J].
Asahi, M ;
Green, NM ;
Kurzydlowski, K ;
Tada, M ;
MacLennan, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) :10061-10066
[4]   Functional co-expression of the canine cardiac Ca2+ pump and phospholamban in Spodoptera frugiperda (Sf21) cells reveals new insights on ATPase regulation [J].
Autry, JM ;
Jones, LR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (25) :15872-15880
[5]  
BRIGGS FN, 1992, J BIOL CHEM, V267, P26056
[6]   Calcium and heart failure: the cycle game [J].
Chien, KR ;
Ross, J ;
Hoshijima, M .
NATURE MEDICINE, 2003, 9 (05) :508-509
[7]   Re-evaluating sarcoplasmic reticulum function in heart failure [J].
Chien, KR .
NATURE MEDICINE, 2000, 6 (09) :942-943
[8]   Current concepts in the treatment of congestive heart failure [J].
Cohn, JN .
CARDIOLOGY, 1997, 88 :2-6
[9]   Gender influences on sarcoplasmic reticulum Ca2+-handling in failing human myocardium [J].
Dash, R ;
Frank, KF ;
Carr, AN ;
Moravec, CS ;
Kranias, EG .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (07) :1345-1353
[10]   Restoration of contractile function in isolated cardiomyocytes from failing human hearts by gene transfer of SERCA2a [J].
del Monte, F ;
Harding, SE ;
Schmidt, U ;
Matsui, T ;
Kang, ZB ;
Dec, W ;
Gwathmey, JK ;
Rosenzweig, A ;
Hajjar, RJ .
CIRCULATION, 1999, 100 (23) :2308-2311