Phospholamban-to-SERCA2 ratio controls the force-frequency relationship

被引:69
作者
Meyer, M
Bluhm, WF
He, HP
Post, SR
Giordano, FJ
Lew, WYW
Dillmann, WH
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pharmacol, La Jolla, CA 92093 USA
[3] Dept Vet Affairs Med Ctr, Dept Med, La Jolla, CA 92093 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1999年 / 276卷 / 03期
关键词
sarcoplasmic reticulum; staircase; contractility; adenovirus; sarcoplasmic reticulum calcium-adenosinetriphosphatase;
D O I
10.1152/ajpheart.1999.276.3.H779
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The force-frequency relationship (FFR) describes the frequency-dependent potentiation of cardiac contractility. The interaction of the sarcoplasmic reticulum Ca2+-adenosinetriphosphatase (SERCA2) with its inhibitory protein phospholamban (PLB) might be involved in the control of the FFR. The FFR was analyzed in two systems in which the PLB-to-SERCA2 ratio was modulated. Adult rabbit cardiac myocytes were transduced with adenovirus encoding for SERCA2, PLB, and beta-galadosidase (control). After 3 days, the relative PLB/SERCA2 values were significantly different between groups (SERCA2, 0.5; control, 1.0; PLB, 4.5). SERCA2 overexpression shortened relaxation by 23% relative to control, whereas PLB prolonged relaxation by 39% and reduced contractility by 47% (0.1 Hz). When the stimulation frequency was increased to 1.5 Hz, myocyte contractility was increased by 30% in control myocytes. PLB-overexpressing myocytes showed an augmented positive FFR (+78%), whereas SERCA2-transduced myocytes displayed a negative FFR (-15%). A more negative FFR was also found in papillary muscles from SERCA2 transgenic mice. These findings demonstrate that the ratio of phospholamban to SERCA2 is an important component in the control of the FFR.
引用
收藏
页码:H779 / H785
页数:7
相关论文
共 28 条
  • [1] INTRACELLULAR CALCIUM HOMEOSTASIS IN CARDIAC MYOCYTES
    BARRY, WH
    BRIDGE, JHB
    [J]. CIRCULATION, 1993, 87 (06) : 1806 - 1815
  • [2] CAMKII IS RESPONSIBLE FOR ACTIVITY-DEPENDENT ACCELERATION OF RELAXATION IN RAT VENTRICULAR MYOCYTES
    BASSANI, RA
    MATTIAZZI, A
    BERS, DM
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1995, 268 (02): : H703 - H712
  • [3] Bers DM, 1991, EXCITATION CONTRACTI, P155
  • [4] Bowditch HP, 1871, BERICHTE KONIG SACHS, V23, P652
  • [5] COMPARATIVE FORCE-FREQUENCY RELATIONSHIPS IN HUMAN AND OTHER MAMMALIAN VENTRICULAR MYOCARDIUM
    BUCKLEY, NM
    LITWAK, RS
    PENEFSKY, ZJ
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1972, 332 (04): : 259 - +
  • [6] ROLE OF CYCLIC ADENOSINE-3',5'-MONOPHOSPHATE AND CALCIUM IN REGULATION OF CONTRACTILITY AND GLYCOGEN-PHOSPHORYLASE ACTIVITY IN GUINEA-PIG PAPILLARY-MUSCLE
    DOBSON, JG
    ROSS, J
    MAYER, SE
    [J]. CIRCULATION RESEARCH, 1976, 39 (03) : 388 - 395
  • [7] Giordano FJ, 1997, CIRCULATION, V96, P400
  • [8] Phorbol myristate acetate-induced hypertrophy of neonatal rat cardiac myocytes is associated with decreased sarcoplasmic reticulum Ca2+ ATPase (SERCA2) gene expression and calcium reuptake
    Hartong, R
    Villarreal, FJ
    Giordano, F
    Dandan, RH
    McDonough, PM
    Dillmann, WH
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1996, 28 (12) : 2467 - 2477
  • [9] Overexpression of the rat sarcoplasmic reticulum Ca2+ ATPase gene in the heart of transgenic mice accelerates calcium transients and cardiac relaxation
    He, HP
    Giordano, FJ
    HilalDandan, R
    Choi, DJ
    Rockman, HA
    McDonough, PM
    Bluhm, WF
    Meyer, M
    Sayen, MR
    Swanson, E
    Dillmann, WH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1997, 100 (02) : 380 - 389
  • [10] Rate-dependent abbreviation of Ca2+ transient in rat heart is independent of phospholamban phosphorylation
    Hussain, M
    Drago, GA
    Colyer, J
    Orchard, CH
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 1997, 273 (02): : H695 - H706