α1-Adrenergic receptor subtypes:: non-identical triplets with different dancing partners?

被引:36
作者
Hague, C [1 ]
Chen, ZJ [1 ]
Uberti, M [1 ]
Minneman, KP [1 ]
机构
[1] Emory Univ, Dept Pharmacol, Atlanta, GA 30322 USA
关键词
adrenergic receptor; norepinepbrine; cardiovascular function; allosteric; dimerization; binding partners;
D O I
10.1016/j.lfs.2003.07.008
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
alpha(1)-Adrenergic receptors are one of the three subfamilies of G protein coupled receptors activated by epinephrine and norepinephrine to control important functions in many target organs. Three human subtypes (alpha(1A), alpha(1B), alpha(1D)) are derived from separate genes and are highly homologous in their transmembrane domains but not in their amino or carboxyl termini. Recent advances in our understanding of these "non-identical triplets" include development of knockout mice lacking single or multiple subtypes, new insights into subcellular localization and trafficking, identification of allosteric modulators, and increasing evidence for an important role in brain function. Although all three subtypes activate the same G(q/11) signaling pathway, they also appear to interact with different protein binding partners. Recent evidence suggests they may also form dimers, and may initiate independent signals through pathways yet to be clearly elucidated. Thus, this subfamily represents a common phenomenon of a group of similar but non-identical receptor subtypes activated by the same neurotransmitter, whose individual functional roles remain to be clearly established. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:411 / 418
页数:8
相关论文
共 51 条
[1]
Control of 5-hydroxytryptamine release in the dorsal raphe nucleus by the noradrenergic system in rat brain.: Role of α-adrenoceptors [J].
Bortolozzi, A ;
Artigas, F .
NEUROPSYCHOPHARMACOLOGY, 2003, 28 (03) :421-434
[2]
Oligomerization of G-protein-coupled transmitter receptors [J].
Bouvier, M .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (04) :274-286
[3]
G protein-coupled receptor interacting proteins: Emerging roles in localization and signal transduction [J].
Brady, AE ;
Limbird, LE .
CELLULAR SIGNALLING, 2002, 14 (04) :297-309
[4]
The molecular architecture of odor and pheromone sensing in mammals [J].
Buck, LB .
CELL, 2000, 100 (06) :611-618
[5]
Decreased blood pressure response in mice deficient of the alpha(1b)-adrenergic receptor [J].
Cavalli, A ;
Lattion, AL ;
Hummler, E ;
Nenniger, M ;
Pedrazzini, T ;
Aubert, JF ;
Michel, MC ;
Yang, M ;
Lembo, G ;
Vecchione, C ;
Mostardini, M ;
Schmidt, A ;
Beermann, F ;
Cotecchia, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11589-11594
[6]
Differences in the cellular localization and agonist-mediated internalization properties of the α1-adrenoceptor subtypes [J].
Chalothorn, D ;
McCune, DF ;
Edelmann, SE ;
García-Cazarín, ML ;
Tsujimoto, G ;
Piascik, MT .
MOLECULAR PHARMACOLOGY, 2002, 61 (05) :1008-1016
[7]
Molecular cloning, genomic characterization and expression of novel human α1A-adrenoceptor isoforms [J].
Chang, DJ ;
Chang, TK ;
Yamanishi, SS ;
Salazar, FHR ;
Kosaka, AH ;
Khare, R ;
Bhakta, S ;
Jasper, JR ;
Shieh, IS ;
Lesnick, JD ;
Ford, APDW ;
Daniels, DV ;
Eglen, RM ;
Clarke, DE ;
Bach, C ;
Chan, HW .
FEBS LETTERS, 1998, 422 (02) :279-283
[8]
alpha(1)-adrenergic receptor signaling via G(h) is subtype specific and independent of its transglutaminase activity [J].
Chen, SH ;
Lin, F ;
Iismaa, S ;
Lee, KN ;
Birckbichler, PJ ;
Graham, RM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32385-32391
[9]
G protein-coupled receptor allosterism and complexing [J].
Christopoulos, A ;
Kenakin, T .
PHARMACOLOGICAL REVIEWS, 2002, 54 (02) :323-374
[10]
A knockout approach indicates a minor vasoconstrictor role for vascular α1B-adrenoceptors in mouse [J].
Daly, CJ ;
Deighan, C ;
McGee, A ;
Mennie, D ;
Ali, Z ;
McBride, M ;
McGrath, JC .
PHYSIOLOGICAL GENOMICS, 2002, 9 (02) :85-91