Genetically encoded tools for in vivo G-protein-coupled receptor agonist detection at cellular resolution

被引:5
|
作者
Kroning, Kayla E. [1 ,2 ,3 ]
Wang, Wenjing [1 ,2 ,3 ]
机构
[1] Univ Michigan, Life Sci Inst, Ann Arbor, MI USA
[2] Univ Michigan, Dept Chem, Ann Arbor, MI USA
[3] Univ Michigan, Life Sci Inst, Ann Arbor, MI 48109 USA
来源
CLINICAL AND TRANSLATIONAL MEDICINE | 2022年 / 12卷 / 12期
关键词
genetically encoded sensor; GPCR; neuromodulation; neurotransmission; STABILIZED ACTIVE STATE; BETA-ARRESTIN; LIVING CELLS; CONFORMATIONAL-CHANGES; NEURAL ACTIVITY; BIASED-AGONISM; ACTIVATION; SENSOR; BIOSENSOR; DOPAMINE;
D O I
10.1002/ctm2.1124
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
G-protein-coupled receptors (GPCRs) are the most abundant receptor type in the human body and are responsible for regulating many physiological processes, such as sensation, cognition, muscle contraction and metabolism. Further, GPCRs are widely expressed in the brain where their agonists make up a large number of neurotransmitters and neuromodulators. Due to the importance of GPCRs in human physiology, genetically encoded sensors have been engineered to detect GPCR agonists at cellular resolution in vivo. These sensors can be placed into two main categories: those that offer real-time information on the signalling dynamics of GPCR agonists and those that integrate the GPCR agonist signal into a permanent, quantifiable mark that can be used to detect GPCR agonist localisation in a large brain area. In this review, we discuss the various designs of real-time and integration sensors, their advantages and limitations, and some in vivo applications. We also discuss the potential of using real-time and integrator sensors together to identify neuronal circuits affected by endogenous GPCR agonists and perform detailed characterisations of the spatiotemporal dynamics of GPCR agonist release in those circuits. By using these sensors together, the overall knowledge of GPCR-mediated signalling can be expanded.
引用
收藏
页数:20
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