Abstract |
The junctional membrane complex between the plasma membrane (PM) and endoplasmic/sarcoplasmic reticulum (ER/SR) is an important structural foundation for functional crosstalk between ionic channels. In cardiac myocytes, functional coupling between cell-surface and intracellular Ca(2+) channels produces Ca(2+) transients for contraction. Junctophilins, a novel family of junctional membrane complex proteins, contribute to the stabilization of the junctional membrane complex by anchoring the ER/SR and interacting with the PM. Mutant mice lacking the cardiac-type junctophilin exhibited embryonic lethality due to heart failure, and the mutant cardiac myocytes showed deficiency of the junctional membrane complexes and abnormal Ca(2+) signaling.
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Authors | H Takeshima |
Journal | Clinical calcium
(Clin Calcium)
Vol. 11
Issue 6
Pg. 758-62
(Jun 2001)
ISSN: 0917-5857 [Print] Japan |
PMID | 15775579
(Publication Type: English Abstract, Journal Article)
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