As the prevalence of type 2 diabetes continues to escalate, there is an urgent need for interventions that effectively prevent diabetic cardiovascular complications, which account for >50% of deaths in this population. Diabetes blocks the cardiac response to multiple prosurvival signaling pathways, rendering cardiomyocytes more susceptible to MI/R injury. The molecular mechanisms leading to "universal" impairment of cardioprotective signaling in the diabetic heart remain unclear. Cav-centered signaling complexes play essential roles in facilitating rapid, precise, and coordinated signal transduction broadly involved in cell protection and survival. However, whether and how Cav-signal complexes are altered and contribute to impairment of cardioprotective signaling remains unknown. Our preliminary experiments demonstrate that nitrative modification of Cav3 and resultant dissociation of Cav3 from its partner proteins occur during the early development phase of type 2 diabetes, blocking Cav3- dependent signaling. The current application will test a hypothesis that, in the diabetic heart, cardioprotective Cav3-signalsomes required by multiple cardioprotective interventions are impaired due to Cav3 nitrative modification at specific Tyr residue(s), resulting in the universal loss of prosurvival cardioprotective signaling cascades, contributing to increased diabetic patient mortality after MI. We will utilize advanced molecular/cellular technologies, and combine in vitro and in vivo approaches to identify the specific tyrosine residue(s) whose nitrative/oxidative modification results in disassembly of cardioprotective Cav3-signalsomes (Specific Aim 1), blocking their biological functions (Specific Aim 2), and reveal novel therapeutic strategies restoring cardioprotective signaling in the diabetic heart (Specific Aim 3), with the ultimate goal of reducing cardiovascular mortality in diabetic individuals. The novel data resulting from this application's proposed studies will define novel molecular mechanisms leading to the loss of cardioprotective response in diabetic heart, and potentially identify novel cardioprotective targets that may preserve/restore various cardioprotective signaling during early developmental diabetic stages.

Public Health Relevance

Cardiovascular disease remains the greatest cause of death, disability, and health care expense in our society. The current application endeavors to define molecular mechanisms leading to increased cardiac injury and mortality in diabetic patients, and identify novel therapeutic strategies capable of blocking/preventing diabetic cardiac injury, for the purpose of ultimately ameliorating morbidity and mortality associated with cardiovascular disease.

Agency
National Institute of Health (NIH)
Type
High Priority, Short Term Project Award (R56)
Project #
1R56HL123404-01
Application #
8903584
Study Section
Myocardial Ischemia and Metabolism Study Section (MIM)
Program Officer
Wang, Lan-Hsiang
Project Start
Project End
Budget Start
Budget End
Support Year
1
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Thomas Jefferson University
Department
Emergency Medicine
Type
Schools of Medicine
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19107