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DREADDs(仅被设计药物激活的设计受体):具有治疗效用的化学遗传学工具。

DREADDs (designer receptors exclusively activated by designer drugs): chemogenetic tools with therapeutic utility.

机构信息

Department of Pharmacology, UNC School of Medicine.

出版信息

Annu Rev Pharmacol Toxicol. 2015;55:399-417. doi: 10.1146/annurev-pharmtox-010814-124803. Epub 2014 Sep 25.

Abstract

In the past decade, emerging synthetic biology technologies such as chemogenetics have dramatically transformed how pharmacologists and systems biologists deconstruct the involvement of G protein-coupled receptors (GPCRs) in a myriad of physiological and translational settings. Here we highlight a specific chemogenetic application that extends the utility of the concept of RASSLs (receptors activated solely by synthetic ligands): We have dubbed it DREADDs (designer receptors exclusively activated by designer drugs). As we show in this review, DREADDs are now used ubiquitously to modulate GPCR activity noninvasively in vivo. Results from these studies have directly implicated GPCR signaling in a large number of therapeutically relevant contexts. We also highlight recent applications of DREADD technology that have illuminated GPCR signaling processes that control pathways relevant to the treatment of eating disorders, obesity, and obesity-associated metabolic abnormalities. Additionally, we provide an overview of the potential utility of chemogenetic technologies for transformative therapeutics.

摘要

在过去的十年中,新兴的合成生物学技术,如化学遗传学,极大地改变了药理学和系统生物学家如何在众多生理和转化环境中解构 G 蛋白偶联受体(GPCR)的参与。在这里,我们重点介绍一种特定的化学遗传学应用,该应用扩展了 RASSLs(仅由合成配体激活的受体)概念的实用性:我们将其称为 DREADDs(仅由设计药物激活的设计受体)。正如我们在本综述中所示,DREADDs 现在被广泛用于在体内非侵入性地调节 GPCR 活性。这些研究的结果直接表明 GPCR 信号在大量治疗相关的情况下起作用。我们还强调了 DREADD 技术的最新应用,这些应用阐明了控制与治疗饮食失调、肥胖和肥胖相关代谢异常相关途径的 GPCR 信号转导过程。此外,我们概述了化学遗传学技术在变革性治疗中的潜在应用。

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