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OLFR734 作为天冬酰胺酶的受体介导葡萄糖代谢。

OLFR734 Mediates Glucose Metabolism as a Receptor of Asprosin.

机构信息

MOE Key Laboratory of Bioinformatics, Tsinghua-Peking Joint Center for Life Sciences, School of Life Sciences, Tsinghua University, 100084 Beijing, China.

National Protein Science Technology Center, Tsinghua University, 100084 Beijing, China.

出版信息

Cell Metab. 2019 Aug 6;30(2):319-328.e8. doi: 10.1016/j.cmet.2019.05.022. Epub 2019 Jun 20.

Abstract

Asprosin is a fasting-induced hormone that promotes glucose production in the liver and stimulates appetite in the hypothalamus by activating the cAMP signaling pathway via an unknown G protein-coupled receptor (GPCR). However, the bona fide receptor of Asprosin is unclear. Here, we have identified that the olfactory receptor OLFR734 acts as a receptor of Asprosin to modulate hepatic glucose production. Olfr734 knockout mice show a blunted response to Asprosin, including attenuated cAMP levels and hepatic glucose production, and improved insulin sensitivity. As Olfr734 deficiency dramatically attenuates both fasting and high-fat-diet-induced glucose production, our results demonstrate a critical role of OLFR734 as a receptor of Asprosin to maintain glucose homeostasis during fasting and in obesity.

摘要

胰高血糖素样肽 1 是一种在禁食诱导下产生的激素,它通过激活未知的 G 蛋白偶联受体 (GPCR) 来激活 cAMP 信号通路,从而促进肝脏中的葡萄糖产生,并刺激下丘脑的食欲。然而,胰高血糖素样肽 1 的真正受体尚不清楚。在这里,我们已经确定嗅觉受体 OLFR734 作为胰高血糖素样肽 1 的受体,以调节肝脏葡萄糖产生。Olfr734 敲除小鼠对胰高血糖素样肽 1 的反应迟钝,包括 cAMP 水平和肝脏葡萄糖产生降低,以及胰岛素敏感性提高。由于 Olfr734 缺乏可显著减弱禁食和高脂肪饮食诱导的葡萄糖产生,因此我们的结果表明 OLFR734 作为胰高血糖素样肽 1 的受体在禁食和肥胖期间维持葡萄糖稳态中起关键作用。

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