G protein-coupled receptor trafficking and signaling: new insights into the enteric nervous system

被引:6
|
作者
Carbone, Simona E. [1 ,2 ]
Veldhuis, Nicholas A. [1 ,2 ]
Gondin, Arisbel B. [1 ,2 ]
Poole, Daniel P. [1 ,2 ,3 ]
机构
[1] Monash Univ, Drug Discovery Biol Theme, Monash Inst Pharmaceut Sci, 381 Royal Parade, Parkville, Vic 3052, Australia
[2] Monash Univ, Australian Res Council Ctr Excellence Convergent, Parkville, Vic, Australia
[3] Univ Melbourne, Anat & Neurosci, Parkville, Vic, Australia
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
endocytosis; enteric nervous system; GPCR; location-specific signaling; receptor trafficking; MU-OPIOID RECEPTOR; NEUROKININ; RECEPTOR; MORPHINE-TOLERANCE; INTERSTITIAL-CELLS; SUBSTANCE-P; NEURONS; ENDOCYTOSIS; AGONIST; LOCALIZATION; LIGAND;
D O I
10.1152/ajpgi.00406.2018
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
G protein-coupled receptors (GPCRs) are essential for the neurogenic control of gastrointestinal (GI) function and are important and emerging therapeutic targets in the gut. Detailed knowledge of both the distribution and functional expression of GPCRs in the enteric nervous system (ENS) is critical toward advancing our understanding of how these receptors contribute to GI function during physiological and pathophysiological states. Equally important, but less well defined, is the complex relationship between receptor expression, ligand binding, signaling, and trafficking within enteric neurons. Neuronal GPCRs are internalized following exposure to agonists and under pathological conditions, such as intestinal inflammation. However, the relationship between the intracellular distribution of GPCRs and their signaling outputs in this setting remains a "black box". This review will briefly summarize current knowledge of agonist-evoked GPCR trafficking and location-specific signaling in the ENS and identifies key areas where future research could be focused. Greater understanding of the cellular and molecular mechanisms involved in regulating GPCR signaling in the ENS will provide new insights into GI function and may open novel avenues for therapeutic targeting of GPCRs for the treatment of digestive disorders.
引用
收藏
页码:G446 / G452
页数:7
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