Abstract
The Ca2+ content in the sarcoplasmic reticulum (SR) determines the amount of Ca2+ released, thereby regulating the magnitude of Ca2+ transient and contraction in cardiac muscle. The Ca2+ content in the SR is known to be regulated by two factors: the activity of the Ca2+ pump (SERCA) and Ca2+ leak through the ryanodine receptor (RyR). However, the direct relationship between the SERCA activity and Ca2+ leak has not been fully investigated in the heart. In the present study, we evaluated the role of the SERCA activity in Ca2+ leak from the SR using a novel saponin-skinned method combined with transgenic mouse models in which the SERCA activity was genetically modulated. In the SERCA overexpression mice, the Ca2+ uptake in the SR was significantly increased and the Ca2+ transient was markedly increased. However, Ca2+ leak from the SR did not change significantly. In mice with overexpression of a negative regulator of SERCA, sarcolipin, the Ca2+ uptake by the SR was significantly decreased and the Ca2+ transient was markedly decreased. Again, Ca2+ leak from the SR did not change significantly. In conclusion, the selective modulation of the SERCA activity modulates Ca2+ uptake, although it does not change Ca2+ leak from the SR.
Original language | English (US) |
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Pages (from-to) | 17-23 |
Number of pages | 7 |
Journal | Cell Calcium |
Volume | 55 |
Issue number | 1 |
DOIs | |
State | Published - Jan 2014 |
Externally published | Yes |
Bibliographical note
Funding Information:This work was supported by a Grant-in-Aid from the Ministry of Education, Culture, Sports, Science and Technology [ 19590833 to K.H., 23790255 to S.M., 18590789 to K.K., 22300130 and 23136515 to S.K.], a Grant-in-Aid for Research on Intractable Diseases, in Health and Labour Sciences Research Grants from the Ministry of Health, Labour and Welfare [to K.H. and M.Y.] the Takeda Science Foundation [to K.H.], the Jikei University Research Fund [to S.M.], the Uehara Memorial Foundation [to S.K.] and the Vehicle Racing Commemorative Foundation [to K.H. and S.K.].
Keywords
- Aequorin
- Cardiac muscle
- Excitation-contraction coupling
- Transgenic mouse