Experimental & Molecular Medicine · 2009 · 42 citations · 34 references
Life SciencesCell BiologyPharmacologyBiochemical PharmacologyCell SignalingCellular MetabolismCardiac PhysiologyCardiovascular Molecular PhysiologyCardiovascular PathophysiologyCardiovascular PhysiologyMitochondrial PhysiologyMitochondrial SignalingCardiac Hypertrophy SignalingCardiac Mitochondrial FunctionCaveolin ProteinsImmunofluorescence ImagingMitochondrial Function In CardiomyocytesProtein Subcellular LocalizationSubcellular Localization MappingSubcellular Protein Localization
We investigated the effect of phenylephrine (PE)- and isoproterenol (ISO)-induced cardiac hypertrophy on subcellular localization and expression of caveolin-3 and STAT3 in H9c2 cardiomyoblast cells. Caveolin-3 localization to plasma membrane was attenuated and localization of caveolin-3 to caveolae in the plasma membrane was 24.3% reduced by the catecholamine- induced hypertrophy. STAT3 and phospho-STAT3 were up-regulated but verapamil and cyclosporin A synergistically decreased the STAT3 and phospho- STAT3 levels in PE- and ISO-induced hypertrophic cells. Both expression and activation of STAT3 were increased in the nucleus by the hypertrophy. Immunofluorescence analysis revealed that the catecholamine- induced hypertrophy promoted nuclear localization of pY705-STAT3. Of interest, phosphorylation of pS727- STAT3 in mitochondria was significantly reduced by catecholamine-induced hypertrophy. In addition, mitochondrial complexes II and III were greatly down- regulated in the hypertrophic cells. Our data suggest that the alterations in nuclear and mitochondrial activation of STAT3 and caveolae localization of caveolin-3 are related to the development of the catecholamine-induced cardiac hypertrophy.
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Hypertensive Urgencies and Emergencies
Bruno Zampaglione, Claudio Pascale, Marco Marchisio et al. · Hypertension · 1996 · 473 citations