This is an ongoing project to study the regulatory mechanisms of eicosanoid synthesis in vascular and blood cells. We have shown that cell-cell interaction plays a major role in PGI2 generation at vascular injury sites. Platelet-derived PGH2 is taken up by subendothelial smooth muscle cells which convert it to PGI2. The platelet-derived PGH2 is also utilized by lymphocytes to synthesize PGI2. The goal of this proposal is to further evaluate the regulatory mechanisms at cellular and molecular levels. Preliminary data from our work reveal that phorbol ester and interleukin-2 elicit a highly selective stimulation of eicosanoid synthesis by cultured human and bovine endothelial cells. Stimulation of eicosanoid synthesis by these compounds appears to depend on de novo protein synthesis. We plan to test the hypothesis that phorbol ester and IL-2 stimulate eicosanoid synthesis via de novo synthesis of PGH synthase. The regulation may reside at the level of transcription. We have observed that unlike its effect on endothelial cells, PMA stimulates platelet to synthesize 12 HETE and the effect is enhanced calcium ionophore. We postulate that the mechanism involved in platelets is due to activation of 12-lipoxygenase. We consider it important to perform additional studies on other non-dividing cells such as macrophage and cells from brain. To test the hypothesis, we propose four specific aims. Biochemical, molecular biology, and cell biology techniques will be employed to provide answers to each of the specific aims. The information derived from this project will be valuable for understanding the generation of eicosanoids which play key role in modulating cerebrovascular thrombosis and brain ischemia. It will shed light on the cell types that contribute to eicosanoid synthesis and the different mechanism underlying various stimulatory conditions. We hope that this basic investigation will enable us to develop better therapeutic strategic for controlling cerebral infarction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
2P50NS023327-04
Application #
3923331
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1988
Total Cost
Indirect Cost
City
Houston
State
TX
Country
United States
Zip Code
77225
Chen, Pei-Feng; Wu, Kenneth K (2009) Two synthetic peptides corresponding to the proximal heme-binding domain and CD1 domain of human endothelial nitric-oxide synthase inhibit the oxygenase activity by interacting with CaM. Arch Biochem Biophys 486:132-40
Wu, Jui-Sheng; Cheung, Wai-Mui; Tsai, Yau-Sheng et al. (2009) Ligand-activated peroxisome proliferator-activated receptor-gamma protects against ischemic cerebral infarction and neuronal apoptosis by 14-3-3 epsilon upregulation. Circulation 119:1124-34
Liou, Jun-Yang; Ellent, David P; Lee, Sang et al. (2007) Cyclooxygenase-2-derived prostaglandin e2 protects mouse embryonic stem cells from apoptosis. Stem Cells 25:1096-103
Liou, Jun-Yang; Lee, Sang; Ghelani, Dipak et al. (2006) Protection of endothelial survival by peroxisome proliferator-activated receptor-delta mediated 14-3-3 upregulation. Arterioscler Thromb Vasc Biol 26:1481-7
Cieslik, Katarzyna A; Deng, Wu-Guo; Wu, Kenneth K (2006) Essential role of C-Rel in nitric-oxide synthase-2 transcriptional activation: time-dependent control by salicylate. Mol Pharmacol 70:2004-14
Deng, Wu-Guo; Tang, Shao-Tzu; Tseng, Hui-Ping et al. (2006) Melatonin suppresses macrophage cyclooxygenase-2 and inducible nitric oxide synthase expression by inhibiting p52 acetylation and binding. Blood 108:518-24
Wu, Kenneth K (2006) Analysis of protein-DNA binding by streptavidin-agarose pulldown. Methods Mol Biol 338:281-90
Lin, Teng-Nan; Cheung, Wai-Mui; Wu, Jui-Sheng et al. (2006) 15d-prostaglandin J2 protects brain from ischemia-reperfusion injury. Arterioscler Thromb Vasc Biol 26:481-7
Wu, Kenneth K (2006) Transcription-based COX-2 inhibition: a therapeutic strategy. Thromb Haemost 96:417-22
Liou, Jun-Yang; Aleksic, Nena; Chen, Shu-Fen et al. (2005) Mitochondrial localization of cyclooxygenase-2 and calcium-independent phospholipase A2 in human cancer cells: implication in apoptosis resistance. Exp Cell Res 306:75-84

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