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DREADD:一种化学遗传GPCR信号平台。

DREADD: a chemogenetic GPCR signaling platform.

作者信息

Zhu Hu, Roth Bryan L

机构信息

Department of Pharmacology, University of North Carolina Chapel Hill Medical School, Chapel Hill, NC (Drs Zhu and Roth).

出版信息

Int J Neuropsychopharmacol. 2014 Oct 31;18(1):pyu007. doi: 10.1093/ijnp/pyu007.

DOI:10.1093/ijnp/pyu007
PMID:25522378
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4368861/
Abstract

Recently, we created a family of engineered G protein-coupled receptors (GPCRs) called DREADD (designer receptors exclusively activated by designer drugs) which can precisely control three major GPCR signaling pathways (Gq, Gi, and Gs). DREADD technology has been successfully applied in a variety of in vivo studies to control GPCR signaling, and here we describe recent advances of DREADD technology and discuss its potential application in drug discovery, gene therapy, and tissue engineering.

摘要

最近,我们创建了一类工程化的G蛋白偶联受体(GPCR),称为DREADD(仅由设计药物激活的设计受体),它可以精确控制三种主要的GPCR信号通路(Gq、Gi和Gs)。DREADD技术已成功应用于各种体内研究以控制GPCR信号传导,在此我们描述DREADD技术的最新进展,并讨论其在药物发现、基因治疗和组织工程中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca6/4368861/6732ef995dbc/ijnppy_pyu007_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca6/4368861/c12162df7446/ijnppy_pyu007_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca6/4368861/6732ef995dbc/ijnppy_pyu007_f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca6/4368861/c12162df7446/ijnppy_pyu007_f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fca6/4368861/6732ef995dbc/ijnppy_pyu007_f0002.jpg

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Annu Rev Pharmacol Toxicol. 2015;55:399-417. doi: 10.1146/annurev-pharmtox-010814-124803. Epub 2014 Sep 25.
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Chemogenetic tools to interrogate brain functions.化学遗传学工具用于研究大脑功能。
Annu Rev Neurosci. 2014;37:387-407. doi: 10.1146/annurev-neuro-071013-014048. Epub 2014 Jun 16.
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Remote control of induced dopaminergic neurons in parkinsonian rats.
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G-Protein-Coupled Receptor (GPCR) Signaling and Pharmacology in Metabolism: Physiology, Mechanisms, and Therapeutic Potential.G蛋白偶联受体(GPCR)在代谢中的信号传导与药理学:生理学、机制及治疗潜力
Biomolecules. 2025 Feb 15;15(2):291. doi: 10.3390/biom15020291.
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