In:
Circulation Research, Ovid Technologies (Wolters Kluwer Health), Vol. 87, No. 9 ( 2000-10-27), p. 739-745
Abstract:
Abstract —Thromboxane A 2 (TxA 2 ) causes platelet aggregation, vasoconstriction, and inhibition of endothelial cell (EC) migration and prevents vascular tube formation via its specific receptors (TP), of which there are two isoforms (TPα and TPβ), both expressed in human ECs. In this study, we demonstrate that the TxA 2 mimetic IBOP increases apoptosis of human ECs and inhibits the phosphorylation of Akt kinase, an intracellular mediator required for cell survival. Treatment with IBOP destroyed EC networks formed on a basement membrane matrix in vitro. To distinguish the role of the TP isoforms, each isoform was expressed in TP-null ECs to create TPα and TPβ ECs. IBOP induced apoptosis and inhibited phosphorylation of Akt kinase in both TPα and TPβ. IBOP increased cAMP levels in TPα but not in TPβ. Apoptosis induced by IBOP in TPα was not affected by either the adenylyl cyclase activator forskolin or the protein kinase A inhibitor 14-22 amide or H-89, whereas that in TPβ was suppressed by forskolin and enhanced by the protein kinase A inhibitor 14-22 amide or H-89, suggesting that the TP isoforms differ in their signal pathways in mediating apoptosis. In conclusion, apoptosis may be the mechanism by which TxA 2 -mediated destruction of vascular structures in ECs occurs; although both TP isoforms induce apoptosis, possibly via inhibiting Akt phosphorylation, the signaling differs in each isoform, in that activation of the adenylyl cyclase pathway prevents apoptosis caused by TPβ, but not by TPα, stimulation.
Type of Medium:
Online Resource
ISSN:
0009-7330
,
1524-4571
DOI:
10.1161/01.RES.87.9.739
Language:
English
Publisher:
Ovid Technologies (Wolters Kluwer Health)
Publication Date:
2000
detail.hit.zdb_id:
1467838-X
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