Cardiovascular disease is the major contributor to morbidity and mortality in Western countries. It is characterized by structural and functional changes of blood vessel's wall that lead to reduced blood flow and eventually occlusion. The integrity of the vascular wall is maintained by homeostatic mechanisms controlled by the endothelium. Stress caused by age, oxidants, mechanical injury, and inflammation can result in endothelial dysfunction leading to remodeling of the vessel wall. We found that thrombin, a key protease of the coagulation cascade and inflammatory response, cleaves the high molecular weight (HMW) forms of basic fibroblast growth factor (FGF-2), a ubiquitous protein with trophic effects on vascular cells. The C-terminal fragment of FGF-2 generated by thrombin is similar to low molecular weight (LMW;18 kDa) FGF-2, and induces vascular cell activation of the mitogen-activated protein kinases ERK-1/2. The N-terminal fragment generated by thrombin cleavage of HMW FGF-2 contains a sequence rich in asymmetric-dimethyl-arginine (ADMA) residues. In free form ADMA inhibits key reactions for blood vessel homeostasis such as nitric oxide synthesis, and its serum levels, elevated in diabetes, renal failure, hypertension, and hypercholesterolemia, correlate with a poor prognosis in cardiovascular patients. We found that thrombin cleavage of HMW FGF-2 dramatically upregulates intracellular ADMA levels in cultured cells. Thus, the C-terminal cleavage product of HMW FGF-2 can activate intracellular signaling and control vascular cell functions, while the N- terminal fragment of FGF-2 generates ADMA, a powerful inhibitor of nitric oxide synthesis. Although degradation of methylarginine-rich proteins is recognized as the major source of free ADMA, the factors controlling this process are unknown. Therefore, we propose to investigate this novel role of FGF-2 in vitro and in vivo. The results of this project can provide relevant information of the pathogenetic mechanisms of vascular injury occurring in hypertension, diabetes, and dyslipidemia, conditions that are all characterized by elevated serum levels of ADMA. The elucidation of these mechanisms will foster the development of new pharmacological tools for the treatment of the cardiovascular disorders associated with these diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Exploratory/Developmental Grants (R21)
Project #
3R21AG028785-02S3
Application #
8082023
Study Section
Special Emphasis Panel (ZRG1-CVS-Q (90))
Program Officer
Kohanski, Ronald A
Project Start
2008-03-01
Project End
2011-02-28
Budget Start
2010-08-15
Budget End
2011-02-28
Support Year
2
Fiscal Year
2010
Total Cost
$30,420
Indirect Cost
Name
New York University
Department
Surgery
Type
Schools of Medicine
DUNS #
121911077
City
New York
State
NY
Country
United States
Zip Code
10016
Yoder, Jordan C; Staisiunas, Paul G; Meltzer, David O et al. (2012) Noise and sleep among adult medical inpatients: far from a quiet night. Arch Intern Med 172:68-70
Ferrari, Giovanni; Terushkin, Vitaly; Wolff, Martin J et al. (2012) TGF-?1 induces endothelial cell apoptosis by shifting VEGF activation of p38(MAPK) from the prosurvival p38? to proapoptotic p38?. Mol Cancer Res 10:605-14
Arora, Vineet M; Chang, Kevin L; Fazal, Arshiya Z et al. (2011) Objective sleep duration and quality in hospitalized older adults: associations with blood pressure and mood. J Am Geriatr Soc 59:2185-6
Arora, Vineet M; Fish, Melissa; Basu, Anirban et al. (2010) Relationship between quality of care of hospitalized vulnerable elders and postdischarge mortality. J Am Geriatr Soc 58:1642-8