Using new lines of transgenic (TG) mice, the investigators will determine the relative role of troponin I (TnI) and phospholamban (PLB) phosphorylation in the enhanced rate of relaxation during beta-adrenergic stimulation in control and acidic conditions. The investigator will also determine the impact of different levels of PLB phosphorylation on the regulation of Ca2+ homeostasis and contractility in the heart. New TG mouse lines will be produced by cross-breeding existing lines of mice: PLB deficient mice, TG mice that express mutated PLB at phosphorylation sites for protein kinase A, TG mice in which cardiac TnI (cTnI) has been replaced by slow skeletal TnI (ssTnI), and control mice that express normal levels of PLB and cTnI. Experiments will be done in the following mice: 1) deficient in PLB and expressing either native cTnI or ssTnI in place of cTnI; 2) expressing mutated PLB and either expressing native cTnI or ssTnI in place of cTnI; and 3) mice that express normal levels of PLB and express either native cTnI or have cTnI replaced by ssTnI. These studies will be performed at several levels of organization: whole heart, skinned fiber bundles from papillary muscles, as well as isolated single myocytes in the presence of absence of different concentrations of the beta-adrenergic agonist, isoproterenol, at pH 7.4 and 6.8. Using these new TG mice the investigator will test the hypothesis that both cTnI and PLB phosphorylation contribute to the enhanced relaxation during beta-adrenergic stimulation. Their relative contribution to the enhanced relaxation during different states of beta-adrenergic stimulation in physiological and pathological conditions will be assessed.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
First Independent Research Support & Transition (FIRST) Awards (R29)
Project #
5R29HL058591-03
Application #
6184395
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Project Start
1998-04-01
Project End
2002-03-31
Budget Start
2000-04-01
Budget End
2001-03-31
Support Year
3
Fiscal Year
2000
Total Cost
$104,647
Indirect Cost
Name
University of Illinois at Chicago
Department
Physiology
Type
Schools of Medicine
DUNS #
121911077
City
Chicago
State
IL
Country
United States
Zip Code
60612
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Huang, L; Wolska, B M; Montgomery, D E et al. (2001) Increased contractility and altered Ca(2+) transients of mouse heart myocytes conditionally expressing PKCbeta. Am J Physiol Cell Physiol 280:C1114-20
Wolska, B M; Vijayan, K; Arteaga, G M et al. (2001) Expression of slow skeletal troponin I in adult transgenic mouse heart muscle reduces the force decline observed during acidic conditions. J Physiol 536:863-70
Evans, C C; Pena, J R; Phillips, R M et al. (2000) Altered hemodynamics in transgenic mice harboring mutant tropomyosin linked to hypertrophic cardiomyopathy. Am J Physiol Heart Circ Physiol 279:H2414-23