Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10766835 | Biochemical and Biophysical Research Communications | 2008 | 6 Pages |
Abstract
The Ca2+ ATPase of sarcoplasmic reticulum has a prominent role in excitation/contraction coupling of cardiac muscle, as it induces relaxation by sequestering Ca2+ from the cytoplasm. The stored Ca2+ is in turn released to trigger contraction. We review here experiments demonstrating that in cardiac myocytes Ca2+ signaling and contractile activation are strongly altered by pharmacological inhibition or transcriptional down-regulation of SERCA. On the other hand, kinetics, and intensity of Ca2+ signaling are improved by SERCA overexpression following delivery of exogenous cDNA by adenovirus vectors. Experiments on adrenergic hypertrophy demonstrate SERCA down-regulation, consistent with its pathogenetic involvement in cardiac hypertrophy and failure, as also shown in other experimental models and clinical studies. Compensation by alternate Ca2+ signaling proteins, including functional activation and increased expression of Na+/Ca2+ exchanger and TRPC proteins has been observed. These compensatory mechanisms, including calcineurin activation, remain to be clarified and are a most important subject of current studies.
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Authors
Giuseppe Inesi, Anand Mohan Prasad, Rajendra Pilankatta,