EXCEED THE SPACE PROVIDED. The heart has endogenous protective mechanisms against oxidative stress-induced damage. The cellular mechanisms that lead to the prevention and protection of myocardial damage, however, have not been defined. Lack of such knowledge interferes with the development of new therapeutic strategies that are designed to prevent and/or treat heart disease. My long-range goal is to identify the signal transduction mechanisms, leading to the protection of adult cardiac myocytes. The objective of this application is to evaluate specifically the role of GATA-4 in cell survival signaling induced by hepatocyte growth factor and endothelin-l. The central hypothesis of the application is that hepatocyte growth factor and endothelin-1 protect cardiac myocytes against oxidative stress-induced cell death, in part, by upregulating cell survival genes via the activation of GATA-4. The hypothesis has been formulated on the basis of strong preliminary data, which suggest that hepatocyte growth factor and endothelin-1 protect cardiac myocytes against oxidative stress and activate GATA-4. The rationale for the proposed research is that, once knowledge of the mechanisms that are responsible for the protection of cardiac myocytes has been obtained, it will lead to new strategies that can be used to prevent and/or treat heart disease, thereby reducing the morbidity and mortality that are associated with this condition. I am uniquely prepared to undertake the proposed research because my laboratory has demonstrated that hepatocyte growth factor and endothelin-1 protect adult cardiac myocytes against oxidative stress and also phosphorylate GATA-4, thus many of the techniques and reagents are already available. The central hypothesis will be tested and the objective of the application accomplished by pursuing two specific aims: 1) Determine the mechanism of GATA-4 activation, and 2) Determine the common mechanism by which hepatocyte growth factor and endothelin-1 protect cardiac myocytes. The proposed work is innovative, because it will combine cellular and animal models of adult cardiac myocytes. It is my expectation that GATA-4 plays an important role in signal transduction for cardiac myocyte protection. These results will be significant because they are expected to provide new agents for preventative and therapeutic interventions for heart disease. In addition, it is expected that the results will fundamentally advance the field of cardiac muscle cell biology. PERFORMANCE SITE ========================================Section End===========================================

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL067340-03
Application #
6834573
Study Section
Cardiovascular and Pulmonary Research A Study Section (CVA)
Program Officer
Liang, Isabella Y
Project Start
2003-01-01
Project End
2006-12-31
Budget Start
2005-01-01
Budget End
2005-12-31
Support Year
3
Fiscal Year
2005
Total Cost
$232,800
Indirect Cost
Name
Georgetown University
Department
Pharmacology
Type
Schools of Medicine
DUNS #
049515844
City
Washington
State
DC
Country
United States
Zip Code
20057
Park, Ah-Mee; Nagase, Hiroko; Liu, Lingling et al. (2011) Mechanism of anthracycline-mediated down-regulation of GATA4 in the heart. Cardiovasc Res 90:97-104
Park, Ah-Mee; Wong, Chi-Ming; Jelinkova, Ludmila et al. (2010) Pulmonary hypertension-induced GATA4 activation in the right ventricle. Hypertension 56:1145-51
Day, Regina M; Matus, Ismael A; Suzuki, Yuichiro J et al. (2009) Plasma levels of retinoids, carotenoids and tocopherols in patients with mild obstructive sleep apnoea. Respirology 14:1134-42
Liu, Lingling; Marcocci, Lucia; Wong, Chi Ming et al. (2008) Serotonin-mediated protein carbonylation in the right heart. Free Radic Biol Med 45:847-54
Lee, Young H; Suzuki, Yuichiro J; Griffin, Autumn J et al. (2008) Hepatocyte growth factor regulates cyclooxygenase-2 expression via beta-catenin, Akt, and p42/p44 MAPK in human bronchial epithelial cells. Am J Physiol Lung Cell Mol Physiol 294:L778-86
Wong, Chi Ming; Cheema, Amrita K; Zhang, Lihua et al. (2008) Protein carbonylation as a novel mechanism in redox signaling. Circ Res 102:310-8
Park, Ah-Mee; Nagase, Hiroko; Kumar, Shilpashree Vinod et al. (2007) Effects of intermittent hypoxia on the heart. Antioxid Redox Signal 9:723-9
Park, Ah-Mee; Nagase, Hiroko; Vinod Kumar, Shilpashree et al. (2007) Acute intermittent hypoxia activates myocardial cell survival signaling. Am J Physiol Heart Circ Physiol 292:H751-7
Suzuki, Yuichiro J; Jain, Vivek; Park, Ah-Mee et al. (2006) Oxidative stress and oxidant signaling in obstructive sleep apnea and associated cardiovascular diseases. Free Radic Biol Med 40:1683-92
Preston, Ioana R; Tang, Guangwen; Tilan, Jason U et al. (2005) Retinoids and pulmonary hypertension. Circulation 111:782-90

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