Department of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458, USA.
Department of Molecular Medicine, The Scripps Research Institute, Jupiter, FL 33458, USA.
Science. 2019 Sep 20;365(6459):1267-1273. doi: 10.1126/science.aau2078. Epub 2019 Aug 15.
Opioids target the μ-opioid receptor (MOR) to produce unrivaled pain management, but their addictive properties can lead to severe abuse. We developed a whole-animal behavioral platform for unbiased discovery of genes influencing opioid responsiveness. Using forward genetics in , we identified a conserved orphan receptor, GPR139, with anti-opioid activity. GPR139 is coexpressed with MOR in opioid-sensitive brain circuits, binds to MOR, and inhibits signaling to heterotrimeric guanine nucleotide-binding proteins (G proteins). Deletion of GPR139 in mice enhanced opioid-induced inhibition of neuronal firing to modulate morphine-induced analgesia, reward, and withdrawal. Thus, GPR139 could be a useful target for increasing opioid safety. These results also demonstrate the potential of as a scalable platform for genetic discovery of G protein-coupled receptor signaling principles.
阿片类药物靶向μ-阿片受体(MOR)以产生无与伦比的疼痛管理效果,但它们的成瘾特性可能导致严重滥用。我们开发了一种全动物行为平台,用于公正地发现影响阿片类药物反应性的基因。我们使用正向遗传学在, 中鉴定出一个保守的孤儿受体 GPR139,具有抗阿片活性。GPR139与 MOR 在阿片敏感的脑回路中共表达,与 MOR 结合,并抑制异三聚体鸟苷核苷酸结合蛋白(G 蛋白)的信号转导。在小鼠中删除 GPR139 增强了阿片类药物诱导的神经元放电抑制,以调节吗啡诱导的镇痛、奖赏和戒断。因此,GPR139 可能是增加阿片类药物安全性的有用靶点。这些结果还表明 作为遗传发现 G 蛋白偶联受体信号传导原理的可扩展平台的潜力。