G Protein-Coupled Receptors: Dynamic Machines for Signaling Pain and Itch

被引:117
作者
Geppetti, Pierangelo [1 ]
Veldhuis, Nicholas A. [2 ,3 ]
Lieu, TinaMarie [2 ,3 ]
Bunnett, Nigel W. [2 ,3 ,4 ]
机构
[1] Univ Florence, Dept Hlth Sci, Clin Pharmacol Unit, I-50139 Florence 6, Italy
[2] Monash Inst Pharmaceut Sci, Melbourne, Vic, Australia
[3] Monash Univ, Ctr Excellence Convergent Bionano Sci & Technol, Australian Res Council, Parkville, Vic 3052, Australia
[4] Univ Melbourne, Dept Pharmacol & Therapeut, Melbourne, Vic 3010, Australia
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
MU-OPIOID RECEPTOR; CONVERTING ENZYME 1; VANILLOID; 4; TRPV4; BETA-ARRESTIN; ACTIVATED RECEPTOR-2; FUNCTIONAL SELECTIVITY; ALLOSTERIC MODULATORS; CRYSTAL-STRUCTURE; BIASED AGONISM; SUBSTANCE-P;
D O I
10.1016/j.neuron.2015.11.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
G protein-coupled receptors (GPCRs) are the major class of sensory proteins and a primary therapeutic target in the pathways to pain and itch. GPCRs are complex signaling machines. Their association with ligands, other receptors, and signaling and regulatory partners induces GPCRs to adopt distinct conformations and to traffic to microdomains within plasma and endosomal membranes. This conformational and positional dynamism controls GPCR signaling in time and space and defines the outcome of receptor activation. An understanding of the dynamic nature of GPCRs within primary sensory neurons and neighboring cells brings new insights into their contributions to the physiology and pathophysiology of pain and itch and provides novel opportunities for therapeutic intervention.
引用
收藏
页码:635 / 649
页数:15
相关论文
共 124 条
[1]   The TGR5 receptor mediates bile acid-induced itch and analgesia [J].
Alemi, Farzad ;
Kwon, Edwin ;
Poole, Daniel P. ;
Lieu, TinaMarie ;
Lyo, Victoria ;
Cattaruzza, Fiore ;
Cevikbas, Ferda ;
Steinhoff, Martin ;
Nassini, Romina ;
Materazzi, Serena ;
Guerrero-Alba, Raquel ;
Valdez-Morales, Eduardo ;
Cottrell, Graeme S. ;
Schoonjans, Kristina ;
Geppetti, Pierangelo ;
Vanner, Stephen J. ;
Bunnett, Nigel W. ;
Corvera, Carlos U. .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (04) :1513-1530
[2]  
[Anonymous], CELL
[3]  
Ayoub Mohammed Akli, 2013, Front Endocrinol (Lausanne), V4, P196, DOI 10.3389/fendo.2013.00196
[4]  
Bardoni R, 2014, NEURON, V81, P1312, DOI 10.1016/j.neuron.2014.01.044
[5]   Cellular and Molecular Mechanisms of Pain [J].
Basbaum, Allan I. ;
Bautista, Diana M. ;
Scherrer, Gregory ;
Julius, David .
CELL, 2009, 139 (02) :267-284
[6]   Why we scratch an itch: the molecules, cells and circuits of itch [J].
Bautista, Diana M. ;
Wilson, Sarah R. ;
Hoon, Mark A. .
NATURE NEUROSCIENCE, 2014, 17 (02) :175-182
[7]   Enhanced morphine analgesia in mice lacking β-arrestin 2 [J].
Bohn, LM ;
Lefkowitz, RJ ;
Gainetdinov, RR ;
Peppel, K ;
Caron, MG ;
Lin, FT .
SCIENCE, 1999, 286 (5449) :2495-2498
[8]   Long-lasting oral analgesic effects of N-protected aminophosphinic dual ENKephalinase inhibitors (DENKIs) in peripherally controlled pain [J].
Bonnard, Elisabeth ;
Poras, Herve ;
Nadal, Xavier ;
Maldonado, Rafael ;
Fournie-Zaluski, Marie-Claude ;
Roques, Bernard P. .
PHARMACOLOGY RESEARCH & PERSPECTIVES, 2015, 3 (02)
[9]   Endogenous Regulation of Visceral Pain via Production of Opioids by Colitogenic CD4+ T Cells in Mice [J].
Boue, Jerome ;
Basso, Lilian ;
Cenac, Nicolas ;
Blanpied, Catherine ;
Rolli-Derkinderen, Malvyne ;
Neunlist, Michel ;
Vergnolle, Nathalie ;
Dietrich, Gilles .
GASTROENTEROLOGY, 2014, 146 (01) :166-175
[10]   Cell-Autonomous Regulation of Mu-Opioid Receptor Recycling by Substance P [J].
Bowman, Shanna L. ;
Soohoo, Amanda L. ;
Shiwarski, Daniel J. ;
Schulz, Stefan ;
Pradhan, Amynah A. ;
Puthenveedu, Manojkumar A. .
CELL REPORTS, 2015, 10 (11) :1925-1936