Towards a systems biology approach of G protein-coupled receptor signalling: Challenges and expectations

被引:16
作者
Heitzler, Domitille [1 ,2 ,3 ]
Crepieux, Pascale [1 ,2 ,3 ]
Poupon, Anne [1 ,2 ,3 ]
Clement, Frederique [4 ]
Fages, Francois [5 ]
Reiter, Eric [1 ,2 ,3 ]
机构
[1] INRA, Unite Physiol Reprod & Comportements, UMR85, BIOS Grp, F-37380 Nouzilly, France
[2] CNRS, UMR6175, F-37380 Nouzilly, France
[3] Haras Nationaux, F-37380 Nouzilly, France
[4] INRIA Paris Rocquencourt, Sisyphe Team, F-78153 Le Chesnay, France
[5] INRIA Paris Rocquencourt, Contraintes Team, F-78153 Le Chesnay, France
关键词
GPCR; Signalling; Pharmacology; Systems biology; Bioinformatics; Modelling; MEDIATED ERK ACTIVATION; BETA-ARRESTIN; BETA-2-ADRENERGIC RECEPTOR; HORMONE RECEPTOR; LIVING CELLS; IN-VIVO; NETWORKS; PHOSPHORYLATION; PATHWAYS; MICROARRAYS;
D O I
10.1016/j.crvi.2009.09.002
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
G protein-coupled receptors (GPCRs) control all the main physiological functions and are targeted by more than 50% of therapeutics. Our perception of GPCRs signalling has grown increasingly complex since it is now accepted that they activate large signalling networks which are integrating the information fluxes into appropriate biological responses. These concepts lead the way to the development of pathway-selective agonists (or antagonists) with fewer side effects. Systems biology approaches focused on GPCR-mediated signalling would help dealing with the huge complexity of these mechanisms therefore speeding-up the discovery of new drug classes. In this review, we present the various technical and conceptual possibilities allowing a systems approach of GPCR-mediated signalling. The main remaining limitations are also discussed. To cite this article: D. Heitzler et al., C. R. Biologies 332 (2009). (C) 2009 Academie des sciences. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:947 / 957
页数:11
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