cytochrome-c-t has been researched along with Adenoviridae-Infections* in 1 studies
1 other study(ies) available for cytochrome-c-t and Adenoviridae-Infections
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Enhanced calcium cycling and contractile function in transgenic hearts expressing constitutively active G alpha o* protein.
In contrast to the other heterotrimeric GTP-binding proteins (G proteins) Gs and Gi, the functional role of G o is still poorly defined. To investigate the role of G alpha o in the heart, we generated transgenic mice with cardiac-specific expression of a constitutively active form of G alpha o1* (G alpha o*), the predominant G alpha o isoform in the heart. G alpha o expression was increased 3- to 15-fold in mice from 5 independent lines, all of which had a normal life span and no gross cardiac morphological abnormalities. We demonstrate enhanced contractile function in G alpha o* transgenic mice in vivo, along with increased L-type Ca2+ channel current density, calcium transients, and cell shortening in ventricular G alpha o*-expressing myocytes compared with wild-type controls. These changes were evident at baseline and maintained after isoproterenol stimulation. Expression levels of all major Ca2+ handling proteins were largely unchanged, except for a modest reduction in Na+/Ca2+ exchanger in transgenic ventricles. In contrast, phosphorylation of the ryanodine receptor and phospholamban at known PKA sites was increased 1.6- and 1.9-fold, respectively, in G alpha o* ventricles. Density and affinity of beta-adrenoceptors, cAMP levels, and PKA activity were comparable in G alpha o* and wild-type myocytes, but protein phosphatase 1 activity was reduced upon G alpha o* expression, particularly in the vicinity of the ryanodine receptor. We conclude that G alpha o* exerts a positive effect on Ca2+ cycling and contractile function. Alterations in protein phosphatase 1 activity rather than PKA-mediated phosphorylation might be involved in hyperphosphorylation of key Ca2+ handling proteins in hearts with constitutive G alpha o activation. Topics: Actin Cytoskeleton; Adenoviridae Infections; Adrenergic beta-Agonists; Animals; Animals, Genetically Modified; Blotting, Northern; Blotting, Western; Calcium; Calcium Channels, L-Type; Calcium Signaling; Cell Separation; Cyclic AMP; Cyclic AMP-Dependent Protein Kinases; Cytochromes c; GTP-Binding Protein alpha Subunits, Gi-Go; Isoproterenol; Mice; Myocardial Contraction; Myocardium; Myocytes, Cardiac; Rats; RNA, Messenger; Ryanodine Receptor Calcium Release Channel; Signal Transduction | 2008 |