Copyright © 2004, European Society of Cardiology
Overexpression of sarcolipin decreases myocyte contractility and calcium transient
Department of Physiology and Cell Biology, 304 Hamilton Hall, 1645 Neil Ave, The Ohio State University College of Medicine and Public Health, Columbus, OH 43210, United States
* Corresponding author. Tel.: +1 614 292 2310; fax: +1 614 292 4888. Email address: periasamy.1{at}osu.edu
Objective: Sarcolipin (SLN) is a novel 31-amino-acid protein associated with the sarcoplasmic reticulum (SR) whose function in cardiac muscle is poorly defined. In this study, we tested the hypothesis that SLN is a regulator of SR Ca2+ transport function by overexpressing SLN in adult rat ventricular myocytes which express low levels of SLN.
Methods: Expression of SLN mRNA in rat tissues was analyzed by Northern blot as well by RT-PCR analysis. To define the role of SLN in cardiac muscle contractility, we overexpressed SLN in adult rat ventricular myocytes using adenoviral gene transfer techniques. Localization of SLN in the adult rat ventricular myocytes was determined using confocal microscopy. Myocyte contractility and calcium transients were measured using edge detection and Fura 2AM.
Results: Our results demonstrate that overexpression of SLN decreased the cell shortening significantly when compared to control myocytes, whereas the time to peak contraction was not altered. In addition, SLN overexpression prolonged the time of 50% relaxation. Calcium transient analysis shows that time to 50% decay of [Ca2+]i was markedly prolonged in SLN-overexpressing myocytes (control –245.0 ± 3.78 vs. SLN –199.0 ± 3.25 ms, p<0.001). However, there were no significant differences in peak amplitudes of [Ca2+]i between SLN-overexpressing and control myocytes. We further demonstrate that SLN is localized within the SR membrane similar to PLB and SR Ca2+ ATPase. Co-immunoprecipitation studies indicate that SLN can physically interact with phospholamban.
Conclusions: We conclude that SLN may play an important role in regulating the SR calcium ATPase pump, possibly by interacting with phospholamban.
KEYWORDS Sarcolipin; Calcium; SERCA; Myocyte; Adenovirus
Time for primary review 19 days
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