Title : Cardiac sarcoplasmic reticulum calcium release and load are enhanced by subcellular cAMP elevations in PI3Kgamma-deficient mice.

Pub. Date : 2005 May 27

PMID : 15860757






7 Functional Relationships(s)
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1 Cardiac sarcoplasmic reticulum calcium release and load are enhanced by subcellular cAMP elevations in PI3Kgamma-deficient mice. Calcium phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
2 Cardiac sarcoplasmic reticulum calcium release and load are enhanced by subcellular cAMP elevations in PI3Kgamma-deficient mice. Cyclic AMP phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
3 The cAMP inhibitor Rp-cAMP eliminated enhanced ECC and SR Ca2+ load in PI3Kgamma-/- without effects in control myocytes. Cyclic AMP phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
4 The cAMP inhibitor Rp-cAMP eliminated enhanced ECC and SR Ca2+ load in PI3Kgamma-/- without effects in control myocytes. Cyclic AMP phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
5 On the other hand, the beta-adrenergic receptor agonist isoproterenol increased I(Ca,L) and Ca2+ transient equally by approximately 2-fold in both PI3Kgamma-/- and PI3Kgamma+/- cardiomyocytes. Isoproterenol phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
6 On the other hand, the beta-adrenergic receptor agonist isoproterenol increased I(Ca,L) and Ca2+ transient equally by approximately 2-fold in both PI3Kgamma-/- and PI3Kgamma+/- cardiomyocytes. Isoproterenol phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus
7 Our results establish that PI3Kgamma reduces cardiac contractility in a highly compartmentalized manner by inhibiting cAMP-mediated SR Ca2+ loading without directly affecting other major modulators of ECC, such as AP and I(Ca,L). Cyclic AMP phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Mus musculus