Optical Approaches for Investigating Neuromodulation and G Protein-Coupled Receptor Signaling

被引:5
|
作者
Marcus, David J. [1 ,2 ,5 ]
Bruchas, Michael R. [1 ,2 ,3 ,4 ,6 ]
机构
[1] Univ Washington, Ctr Neurobiol Addict Pain & Emot, Seattle, WA USA
[2] Univ Washington, Dept Anesthesiol & Pain Med, Seattle, WA USA
[3] Univ Washington, Dept Pharmacol, Seattle, WA USA
[4] Univ Washington, Dept Bioengn, Seattle, WA USA
[5] Univ Washington, J181 Hlth Sci,1959 NE Pacific St, Seattle, WA 98195 USA
[6] Univ Washington, 1959 NE Pacific St,J187a Hlth Sci, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
PHOTOSENSITIVE PROTECTING GROUP; CIS-TRANS PHOTOISOMERIZATION; IN-VIVO; ECTOPIC EXPRESSION; NEUROTRANSMITTER RELEASE; OPTOGENETIC INHIBITION; SPATIOTEMPORAL CONTROL; CHEMOKINE RECEPTOR; ADENYLYL-CYCLASE; LIGHT ACTIVATION;
D O I
10.1124/pharmrev.122.000584
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Despite the fact that roughly 40% of all US Food and Drug Administration (FDA)-approved pharmacological therapeutics target G protein- coupled receptors (GPCRs), there remains a gap in our understanding of the physiologic and functional role of these receptors at the systems level. Although heterologous expression systems and in vitro assays have revealed a tremendous amount about GPCR signaling cascades, how these cascades interact across cell types, tissues, and organ systems remains obscure. Classic behavioral pharmacology experiments lack both the temporal and spatial resolution to re-solve these long-standing issues. Over the past half century, there has been a concerted effort toward the development of optical tools for understanding GPCR signaling. From initial ligand uncaging approaches to more recent development of optogenetic techniques, these strategies have allowed researchers to probe longstanding questions in GPCR pharmacology both in vivo and in vitro. These tools have been employed across biologic systems and have allowed for interrogation of everything from specific intramolecular events to pharmacology at the systems level in a spatiotemporally specific manner. In this review, we present a historical perspective on the motivation behind and development of a variety of optical tool -kits that have been generated to probe GPCR signaling. Here we highlight how these tools have been used in vivo to uncover the functional role of distinct populations of GPCRs and their signaling cascades at a systems level.
引用
收藏
页码:1119 / 1139
页数:21
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