Adenosine receptors: G protein-mediated signalling and the role of accessory proteins

被引:236
作者
Klinger, M [1 ]
Freissmuth, M [1 ]
Nanoff, C [1 ]
机构
[1] Univ Vienna, Inst Pharmacol, A-1090 Vienna, Austria
基金
奥地利科学基金会;
关键词
adenosine receptors; G proteins; accessory proteins in signalling;
D O I
10.1016/S0898-6568(01)00235-2
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ever since the discovery of the effects of adenosine in the circulation, adenosine receptors continue to represent a promising drug target. Firstly, this is due to the fact that the receptors are expressed in a large variety of cells; in particular, the actions of adenosine (or, respectively, of the antagonistic methylxanthines) in the central nervous system, in the circulation, on immune cells and on other tissues can beneficial in certain disorders. Secondly, there exists a large number of ligands, which have been generated by introducing several modifications in the structure Of the lead compounds (adenosine and methylxanthine), some of them highly specific. Four adenosine receptor subtypes have been identified by molecular cloning; they belong to the family of G protein-coupled receptors, which transfer signals by activating heterotrimeric G proteins, It has been appreciated recently that accessory proteins impinge on the rcceptor/G protein interaction and thus modulate the signalling reaction, These accessory components may be thought as adaptors that redirect the signalling pathway to elicit a cell-specific response, Here, we review (he recent literature on adenosine receptors and place a focus on the role of accessory proteins in the Organisation of adenosine receptor signalling. These components have been involved in receptor sorting, in the control of signal amplification and in the temporal regulation of receptor activity, while the existence of others is postulated on the basis of atypical cellular reactions elicited by receptor activation. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:99 / 108
页数:10
相关论文
共 123 条
[81]   Stimulation of A2A adenosine receptor phosphorylation by protein kinase C activation:: Evidence for regulation by-multiple protein kinase C isoforms [J].
Palmer, TM ;
Stiles, GL .
BIOCHEMISTRY, 1999, 38 (45) :14833-14842
[82]   Structure-function analysis of inhibitory adenosine receptor regulation [J].
Palmer, TM ;
Stiles, GL .
NEUROPHARMACOLOGY, 1997, 36 (09) :1141-1147
[83]  
PALMER TM, 1994, MOL PHARMACOL, V45, P1082
[84]   Molecular basis for subtype-specific desensitization of inhibitory molecular adenosine receptors - Analysis of a chimeric A(1)-A(3) adenosine receptor [J].
Palmer, TM ;
Benovic, JL ;
Stiles, GL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (25) :15272-15278
[85]  
PALMER TM, 1999, BIOCHEMISRY, V36, P832
[86]   European Stroke Prevention Study-2 results: serendipitous demonstration of neuroprotection induced by endogenous adenosine accumulation? [J].
Picano, E ;
Abbracchio, MP .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1998, 19 (01) :14-16
[87]   G protein-coupled receptor kinases [J].
Pitcher, JA ;
Freedman, NJ ;
Lefkowitz, RJ .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :653-692
[88]  
Ralevic V, 1998, PHARMACOL REV, V50, P413
[89]  
RAMKUMAR V, 1993, J BIOL CHEM, V268, P16887
[90]  
RAMKUMAR V, 1991, MOL PHARMACOL, V40, P639