Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/9611
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Type: Journal article
Title: Roles of cyclooxygenase (COX)-1 and COX-2 in prostanoid production by human endothelial cells: Selective up-regulation of prostacyclin synthesis by COX-2
Author: Caughey, G.
Cleland, L.
Penglis, P.
Gamble, J.
James, M.
Citation: Journal of Immunology, 2001; 167(5):2831-2838
Publisher: Amer Assoc Immunologists
Issue Date: 2001
ISSN: 0022-1767
1550-6606
Abstract: The two cyclooxygenase (COX) isoforms, COX-1 and COX-2, both metabolize arachidonic acid to PGH(2), the common substrate for thromboxane A(2) (TXA(2)), prostacyclin (PGI(2)), and PGE(2) synthesis. We characterized the synthesis of these prostanoids in HUVECs in relation to COX-1 and COX-2 activity. Untreated HUVEC expressed only COX-1, whereas addition of IL-1beta caused induction of COX-2. TXA(2) was the predominant COX-1-derived product, and TXA(2) synthesis changed little with up-regulation of COX-2 by IL-1beta (2-fold increase). By contrast, COX-2 up-regulation was associated with large increases in the synthesis of PGI(2) and PGE(2) (54- and 84-fold increases, respectively). Addition of the selective COX-2 inhibitor, NS-398, almost completely abolished PGI(2) and PGE(2) synthesis, but had little effect on TXA(2) synthesis. The up-regulation of COX-2 by IL-1beta was accompanied by specific up-regulation of PGI synthase and PGE synthase, but not TX synthase. An examination of the substrate concentration dependencies showed that the pathway of TXA(2) synthesis was saturated at a 20-fold lower arachidonic acid concentration than that for PGI(2) and PGE(2) synthesis. In conclusion, endothelial prostanoid synthesis appears to be differentially regulated by the induction of COX-2. The apparent PGI(2) and PGE(2) linkage with COX-2 activity may be explained by a temporal increase in total COX activity, together with selective up-regulation of PGI synthase and PGE synthase, and different kinetic characteristics of the terminal synthases. These findings have particular importance with regard to the potential for cardiovascular consequences of COX-2 inhibition.
Keywords: Endothelium, Vascular; Cells, Cultured; Humans; Aspirin; Cytochrome P-450 Enzyme System; Isoenzymes; Intramolecular Oxidoreductases; Thromboxane-A Synthase; Mitogen-Activated Protein Kinases; Prostaglandins; Dinoprostone; Epoprostenol; Thromboxane A2; Membrane Proteins; Interleukin-1; Cyclooxygenase Inhibitors; Enzyme Induction; Up-Regulation; Kinetics; Prostaglandin-Endoperoxide Synthases; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase 2 Inhibitors; Prostaglandin-E Synthases
RMID: 0020011083
DOI: 10.4049/jimmunol.167.5.2831
Appears in Collections:Medicine publications

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