The AT(2) receptor selectively associates with G(i alpha 2) and G(i alpha 3) in the rat fetus

被引:107
作者
Zhang, JS [1 ]
Pratt, RE [1 ]
机构
[1] STANFORD UNIV, SCH MED, FALK CARDIOVASC RES CTR, DIV CARDIOVASC MED, STANFORD, CA 94305 USA
关键词
D O I
10.1074/jbc.271.25.15026
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effects of angiotensin II are mediated by a family of seven transmembrane receptors. In the adult, the majority of the receptors are of the AT(1) isoform, which is coupled to heterotrimeric G proteins (either G(q alpha) or G(i alpha)). In contrast, the AT(2) receptor is expressed at low levels in the adult but is the major form expressed in the fetal and neonatal animal. Previous results have failed to show G protein coupling of the AT(2) receptor in the fetus. We now provide evidence that the AT(2) receptor is G protein-coupled. An antibody that binds several G(alpha) subunits immunoselected angiotensin II receptor-G(alpha) complexes. In addition, G(i alpha 1-3) antibody, which recognizes G(i alpha 1), G(i alpha 2) and G(i alpha 3), also co-immunoselect the AT(2) recep tor. Anti-G(i alpha 2) and anti-G(i alpha 3) antibodies were both able to co-immunoselected AT(2) receptor-G(i alpha) complexes, but consistent with the lack of G(i alpha 1) in the fetal extracts, anti-G(i alpha 1), antibodies did not nor did any other G protein-directed antisera. The finding that AT(2) receptor couples to both G(i alpha 2) and G(i alpha 3) raises the possibility that selective interactions between AT(2) receptor and different G proteins may result in specific cellular effects mediated by AT(2) stimulation.
引用
收藏
页码:15026 / 15033
页数:8
相关论文
共 49 条
[1]  
ALBLAS J, 1993, J BIOL CHEM, V268, P22235
[2]  
BAUKAL AJ, 1994, J BIOL CHEM, V269, P24546
[3]   RECEPTOR-EFFECTOR COUPLING BY G-PROTEINS [J].
BIRNBAUMER, L ;
ABRAMOWITZ, J ;
BROWN, AM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1031 (02) :163-224
[4]   ANGIOTENSIN-II AT2 RECEPTORS DO NOT INTERACT WITH GUANINE-NUCLEOTIDE BINDING-PROTEINS [J].
BOTTARI, SP ;
TAYLOR, V ;
KING, IN ;
BOGDAL, Y ;
WHITEBREAD, S ;
DEGASPARO, M .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1991, 207 (02) :157-163
[5]   ANGIOTENSIN-II RECEPTOR SUBTYPES - CHARACTERIZATION, SIGNALING MECHANISMS, AND POSSIBLE PHYSIOLOGICAL IMPLICATIONS [J].
BOTTARI, SP ;
DEGASPARO, M ;
STECKELINGS, UM ;
LEVENS, NR .
FRONTIERS IN NEUROENDOCRINOLOGY, 1993, 14 (02) :123-171
[6]   PURIFICATION AND CHARACTERIZATION OF ANGIOTENSIN-II AT(2)-RECEPTORS FROM NEONATAL RAT-KIDNEY [J].
CIUFFO, GM ;
HEEMSKERK, FMJ ;
SAAVEDRA, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (23) :11009-11013
[7]  
CODINA J, 1991, METHOD ENZYMOL, V195, P177
[8]  
DUDLEY DT, 1990, MOL PHARMACOL, V38, P370
[9]   MOLECULAR MECHANISMS OF VASCULAR RENIN-ANGIOTENSIN SYSTEM IN MYOINTIMAL HYPERPLASIA [J].
DZAU, VJ ;
GIBBONS, GH ;
PRATT, RE .
HYPERTENSION, 1991, 18 (04) :100-105
[10]  
EDWARDS RM, 1993, J AM SOC NEPHROL, V3, P1643