Kinase independent function of PI3Kγ modulates calcium re-uptake by regulating phospholamban function

Abstract

AbstractRationaleGenetic deletion of Phosphoinositide 3-kinase (PI3Kγ) in mice (PI3Kγ−/−) results in increased cAMP levels and enhanced ventricular rate/contractility. Whether PI3Kγ plays a role in cardiac contractility by altering intracellular calcium recycling is not known.ObjectiveTo understand the mechanism of PI3Kγ mediated regulation of cardiac contractility.Methods and ResultsCaffeine treatment of adult cardiomyocytes from PI3Kγ−/− mice showed significantly reduced calcium reuptake by sarcoendoplasmic reticulum (SR) indicating that PI3Kγ locally regulates SR function. This resulted in elevated levels of intracellular calcium for prolonged period following caffeine. Our findings show that delayed re-uptake of calcium was caused by changes in phosphorylation of phospholamban (PLN), a major regulator of SR calcium reuptake. PI3Kγ−/− cardiomyocytes show significantly reduced PLN phosphorylation due to increase in PLN-associated protein phosphatase (PP) activity as reflected by decreased demethylated-PP2A. Consistently, the altered calcium regulation in the cardiomyocytes of PI3Kγ−/− can be restored by inhibition of PP by okadaic acid. Unexpectedly, cardiomyocyate-specific overexpression of kinase-dead PI3Kγ PI3Kγinact) in the global PI3Kγ−/− cardiomyocytes normalized caffeine induced calcium reuptake, restored PLN phosphorylation, and decreased PLN-associated PP activity reflected by increased demethylated-PP2A.ConclusionsThese studies bring-to-fore an unrecognized regulation of PLN by PI3Kγ through PP2A with implications in deleterious cardiac remodeling as PI3Kγ is significantly upregulated following cardiac stress.