Differential regulation of thrombospondin-1 and fibronectin by angiotensinII receptor subtypes in cultured endothelial cells

Citation
Jw. Fischer et al., Differential regulation of thrombospondin-1 and fibronectin by angiotensinII receptor subtypes in cultured endothelial cells, CARDIO RES, 51(4), 2001, pp. 784-791
Citations number
48
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
CARDIOVASCULAR RESEARCH
ISSN journal
00086363 → ACNP
Volume
51
Issue
4
Year of publication
2001
Pages
784 - 791
Database
ISI
SICI code
0008-6363(200109)51:4<784:DROTAF>2.0.ZU;2-M
Abstract
Objectives: Angiotensin II (ANG II) can modulate cellular proliferation in various cell types via AT(1) and AT(2), receptors. In the present study, we investigated the effect of the angiotensin AT(1) and AT(2) receptors on DN A-synthesis as well as on the expression of the extracellular matrix (ECM) components, thrombospondin-1 (TSP-1) and fibronectin (FN) in endothelial ce lls (EC). Methods: The experiments were performed in microvascular EC deriv ed from rat heart (CEC) and macrovascular EC derived from bovine aorta (BAE C). The experiments were performed in cells of the second and third passage and the expression of AT(1) and AT(2) receptors was verified by binding st udies, Northern analysis or RT-PCR. Quiescent rat CEC and BAEC were stimula ted to proliferate by the addition of 25 ng/ml bFGF, while ANG II (10(-7) M ) and the selective ANG II receptor antagonists, Losartan (10(-5) M) and PD 123177 (10(-6) M) or the AT, agonist, CGP42112A (10(-7) M) were added 16 h later. Results: ANG II induced a dose-dependent decrease of DNA-synthesis i n BAEC measured by [H-3]-thymidine incorporation. This inhibitory effect of ANG II was prevented by the addition of the AT(2) receptor antagonist PD12 3177 (10(-6) M), demonstrating, that the inhibition of DNA synthesis is med iated by the AT(2) receptor. In the presence of Losartan, stimulation of bo th, CEC and BAEC, with ANG II resulted in a marked increase of TSP-1 mRNA l evels, which was maximal between 3 and 6 h in rat CEC and after 9 h in BAEC . In addition, TSP-1 was clearly induced by the AT(2) agonist CGP42112A. In contrast, blockade of the AT(2) receptor by the selective AT(2) antagonist , PD123177 (10(-6) M), resulted in a pronounced down regulation of FN mRNA 9 h after the stimulation. Conclusions: The present results suggest that th e ANG II receptor subtype AT(2) mediates growth inhibition in macrovascular EC similar to what has been shown before in microvascular rat EC and that AT(2) receptors mediates remodeling of the endothelial ECM by upregulation of TSP-1 expression in both macro- and micro-vascular endothelial cells. (C ) 2001 Elsevier Science B.V. All rights reserved.