Recent Progress in Molecular Mechanisms of Angiotensin II Type 1 and 2 Receptors

被引:1
|
作者
Miura, Shin-ichiro [1 ,2 ,4 ]
Imaizumi, Satoshi [1 ,2 ]
Saku, Keijiro [1 ,2 ,3 ]
机构
[1] Fukuoka Univ, Sch Med, Dept Cardiol, Fukuoka 8140180, Japan
[2] Fukuoka Univ, Sch Med, Dept Mol Cardiovasc Therapeut, Fukuoka 8140180, Japan
[3] Fukuoka Univ, Sch Med, Dept Adv Therapeut Cardiovasc Dis, Fukuoka 8140180, Japan
[4] Cleveland Clin Fdn, Dept Mol Cardiol, Cleveland, OH USA
关键词
Angiotensin II receptors; G protein-coupled receptor; structure and function; PROTEIN-COUPLED RECEPTORS; LIGAND-BINDING POCKET; CYSTEINE-SCANNING MUTAGENESIS; BETA(2) ADRENERGIC-RECEPTOR; 3RD TRANSMEMBRANE DOMAIN; MEDIATED CELL-GROWTH; AT(1) RECEPTOR; CONSTITUTIVE ACTIVATION; CRYSTAL-STRUCTURE; CARDIAC MYOCYTES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The renin-angiotensin system hormone angiotensin II (Ang II) plays a central role in the pathophysiology of vasoconstriction, cardiovascular hypertrophy and hyperplasia. Two distinct subtypes of Ang II receptor, type 1 (AT(1)) and type 2 (AT(2)), have been identified, and both have been shown to belong to the G protein-coupled receptors (GPCRs) superfamily. AT(1) and AT(2) receptors may have antagonistic action. While the crystal structures of GPCRs obtained from the rhodopsin, opsin, and beta(1) and beta(2)-adrenergic receptors have recently been described in different conformational states, the crystal structures of Ang II receptors have not been elucidated. The conformation range and dynamics of the effects of ligands on GPCRs may differ from one receptor to another. This review focuses on the structure and function of Ang II receptors, such as the movement of transmembrane helices, functional selectivity for AT(1) receptor activation, the possibility of constitutive activity of wild-type Ang II receptors and the homo-and hetero-dimerization of Ang II receptors.
引用
收藏
页码:2981 / 2987
页数:7
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