The Core will manage animals (rabbits and mice) from which myocytes will be isolated at Loyola for use in all? 4 of the projects. The mice used will include wild type and genetically modified mice that are developed and? bred in Core D at UCSD (including some that will be subjected to transverse aortic banding to induce? chronic pressure overload in Project by Brown). The rabbits used will include both control and heart failure (HF)? rabbits (induced by combined pressure and volume overload). The core will also be responsible for the? preparation and functional monitoring of HF rabbits during the evolution of dysfunction (under the direction? of Dr. S.M. Pogwizd at UIC). The core will also culture adult cardiac myocytes for 24-48 hours for studies? involving adenoviral gene transfer. These myocytes will be used directly by the three Loyola projects (l-lll)? for functional, imaging and biochemical analysis and also by Project by Brown for biochemical analysis (after? experimental treatment by the investigators at Loyola and shipment to UCSD). The procedures carried out? are specialized, but the personnel involved are expert in their respective roles and this should run smoothly? and efficiently in making the best use of the myocytes available.? Mice are especially valuable because of the opportunity to genetically manipulate the molecules under? investigation (and we are taking advantage of that in The Genetic Mouse Models and Adenoviruses Core) and collectively we have extensive experience? with mouse myocytes and cardiovascular disease models. The mouse work will be complemented by? studies in rabbit, where similar genetic manipulation is not practical, but rabbits are highly advantageous? here for two major reasons. First, the electrophysiological and Ca handling properties in rabbit ventricle are? very similar to that in human. Second, we have already developed a well-characterized rabbit model of? heart failure. Indeed, the HF rabbits manifest both severely depressed LV contractile function and? spontaneously-occurring ventricular arrhythmias. Rabbit myocytes are also well suited for the measurements? to be made (including: voltage clamp, fluorescence imaging, biochemical and molecular studies, and? in vitro adenoviral gene transfer. The services provided by this core are essential to the successful? completion of the science in Projects by Bers, Blatter, Mignery, and Brown, enabling the elucidation of mechanistic roles of IP3R and CaMKII in ECC, arrhythmogenesis, hypertrophy and HF.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
1P01HL080101-01A1
Application #
7139947
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2005-12-01
Project End
2010-11-30
Budget Start
2005-12-01
Budget End
2006-11-30
Support Year
1
Fiscal Year
2006
Total Cost
$253,272
Indirect Cost
Name
Loyola University Chicago
Department
Type
DUNS #
791277940
City
Maywood
State
IL
Country
United States
Zip Code
60153
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Willeford, Andrew; Suetomi, Takeshi; Nickle, Audrey et al. (2018) CaMKII?-mediated inflammatory gene expression and inflammasome activation in cardiomyocytes initiate inflammation and induce fibrosis. JCI Insight 3:
Wood, Brent M; Simon, Mitchell; Galice, Samuel et al. (2018) Cardiac CaMKII activation promotes rapid translocation to its extra-dyadic targets. J Mol Cell Cardiol 125:18-28
Hegyi, Bence; Bossuyt, Julie; Ginsburg, Kenneth S et al. (2018) Altered Repolarization Reserve in Failing Rabbit Ventricular Myocytes: Calcium and ?-Adrenergic Effects on Delayed- and Inward-Rectifier Potassium Currents. Circ Arrhythm Electrophysiol 11:e005852
Yan, Jiajie; Zhao, Weiwei; Thomson, Justin K et al. (2018) Stress Signaling JNK2 Crosstalk With CaMKII Underlies Enhanced Atrial Arrhythmogenesis. Circ Res 122:821-835
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Bovo, Elisa; Huke, Sabine; Blatter, Lothar A et al. (2017) The effect of PKA-mediated phosphorylation of ryanodine receptor on SR Ca2+ leak in ventricular myocytes. J Mol Cell Cardiol 104:9-16
Kanaporis, Giedrius; Blatter, Lothar A (2017) Alternans in atria: Mechanisms and clinical relevance. Medicina (Kaunas) 53:139-149
Yuen, Garrick K; Galice, Samuel; Bers, Donald M (2017) Subcellular localization of Na/K-ATPase isoforms in ventricular myocytes. J Mol Cell Cardiol 108:158-169
Gray, Charles B B; Suetomi, Takeshi; Xiang, Sunny et al. (2017) CaMKII? subtypes differentially regulate infarct formation following ex vivo myocardial ischemia/reperfusion through NF-?B and TNF-?. J Mol Cell Cardiol 103:48-55

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