EVIDENCE FOR A NOVEL ANGIOTENSIN-II RECEPTOR INVOLVED IN ANGIOGENESIS IN CHICK-EMBRYO CHORIOALLANTOIC MEMBRANE

被引:127
作者
LENOBLE, FAC
SCHREURS, NHJS
VANSTRAATEN, HWM
SLAAF, DW
SMITS, JFM
ROGG, H
STRUIJKERBOUDIER, HAJ
机构
[1] UNIV LIMBURG, CARDIOVASC RES INST MAASTRICHT, DEPT ANAT EMBRYOL, 6200 MD MAASTRICHT, NETHERLANDS
[2] UNIV LIMBURG, CARDIOVASC RES INST MAASTRICHT, DEPT BIOPHYS, 6200 MD MAASTRICHT, NETHERLANDS
[3] CIBA GEIGY AG, DIV PHARMACEUT, RES DEPT, CH-4002 BASEL, SWITZERLAND
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1993年 / 264卷 / 02期
关键词
ANGIOGENESIS; ANGIOTENSIN-II; ANGIOTENSIN RECEPTOR; CHORIOALLANTOIC MEMBRANE; HYPERTENSION;
D O I
10.1152/ajpregu.1993.264.2.R460
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Angiotensin II acts as a growth factor in the cardiovascular system and has been implicated in angiogenesis. The existence of at least two types of angiotensin II receptors, the AT1 and the AT2 receptors, has been suggested by ligand binding studies. We used three different AT receptor antagonists to study the receptor mediating angiotensin II-induced angiogenesis in the chorioallantoic membrane (CAM) of the chick embryo. Angiotensin II caused pronounced angiogenesis of pre- and postcapillary vessels of 30-40%. This response could only be blocked by adding the peptidergic AT2 antagonist CGP-42112A. The nonpeptidergic AT2 antagonist PD123319 and AT1 antagonist losartan (DuP 753) were not effective. In addition, we used radioligand binding studies with a range of ligands to define the nature of the receptor. Our results show a high density of specific single class AT receptor with a total number of binding sites of 1,190 fmol/mg protein and an affinity constant for angiotensin II of 2.7 nM. The inhibitory concentrations (IC50) for CGP-42112A, PD 123319 and losartan were 724 > 100,000, and 59,000 nM, respectively. Our studies suggest that these binding sites act as receptors for angiotensin II-induced angiogenesis. Both functional and radioligand binding studies suggest that the receptor is different from the classical mammalian AT1 and AT2 receptors.
引用
收藏
页码:R460 / R465
页数:6
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