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利用DREADD基因敲入小鼠对GPCR信号的组织特异性和时间激活进行成像。

Imaging of Tissue-Specific and Temporal Activation of GPCR Signaling Using DREADD Knock-In Mice.

作者信息

Akhmedov Dmitry, Kirkby Nicholas S, Mitchell Jane A, Berdeaux Rebecca

机构信息

Department of Integrative Biology and Pharmacology, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, TX, USA.

Cardiothoracic Pharmacology, National Heart and Lung Institute, Imperial College London, London, UK.

出版信息

Methods Mol Biol. 2019;1947:361-376. doi: 10.1007/978-1-4939-9121-1_21.

Abstract

Engineered G protein-coupled receptors (DREADDs, designer receptors exclusively activated by designer drugs) are convenient tools for specific activation of GPCR signaling in many cell types. DREADDs have been utilized as research tools to study numerous cellular and physiologic processes, including regulation of neuronal activity, behavior, and metabolism. Mice with random insertion transgenes and adeno-associated viruses have been widely used to express DREADDs in individual cell types. We recently created and characterized ROSA26-GsDREADD knock-in mice to allow Cre recombinase-dependent expression of a Gαs-coupled DREADD (GsD) fused to GFP in distinct cell populations in vivo. These animals also harbor a CREB-activated luciferase reporter gene for analysis of CREB activity by in vivo imaging, ex vivo imaging, or biochemical reporter assays. In this chapter, we provide detailed methods for breeding GsD animals, inducing GsD expression, stimulating GsD activity, and measuring basal and stimulated CREB reporter bioluminescence in tissues in vivo, ex vivo, and in vitro. These animals are available from our laboratory for non-profit research.

摘要

工程化G蛋白偶联受体(DREADDs,即仅由设计药物激活的设计受体)是在多种细胞类型中特异性激活GPCR信号传导的便捷工具。DREADDs已被用作研究工具来研究众多细胞和生理过程,包括神经元活动、行为和代谢的调节。具有随机插入转基因的小鼠和腺相关病毒已被广泛用于在个体细胞类型中表达DREADDs。我们最近创建并表征了ROSA26-GsDREADD敲入小鼠,以允许在体内不同细胞群体中Cre重组酶依赖性表达与GFP融合的Gαs偶联DREADD(GsD)。这些动物还携带一个CREB激活的荧光素酶报告基因,用于通过体内成像、体外成像或生化报告分析来分析CREB活性。在本章中,我们提供了繁殖GsD动物、诱导GsD表达、刺激GsD活性以及在体内、体外和离体组织中测量基础和刺激后的CREB报告基因生物发光的详细方法。这些动物可从我们实验室获取用于非营利性研究。

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