Dept. of Metabolic Disorders, Amgen Inc., 1120 Veterans Blvd., South San Francisco, CA 94080, USA.
Biochem Biophys Res Commun. 2012 Feb 3;418(1):1-5. doi: 10.1016/j.bbrc.2011.11.117. Epub 2011 Dec 1.
GPR21 is an orphan G-protein-coupled receptor. We found that mice deficient for the GPR21 gene were resistant to diet-induced obesity. Knockout mice were leaner than their wildtype counterpart, despite that no difference was observed in food intake. No differences were observed in the respiratory exchange rate and thermogenesis. However, knockout mice were more active than wildtype littermates, and this level of activity may be an underlying reason for the difference in energy balance. Mutant mice were more sensitive to insulin than their wildtype control and showed an improved glucose tolerance. Several inflammatory markers MCP-1, CRP and IP-10 were decreased in mutant animals, suggesting that GPR21 may also mediate its effect through anti-inflammatory mechanisms. We found that GPR21 is widely expressed in all tissues, with the highest levels found in the brain and in the spleen. Overall, these findings suggest that GPR21 may play an important role in regulating body weight and glucose metabolism.
GPR21 是一种孤儿 G 蛋白偶联受体。我们发现,缺乏 GPR21 基因的小鼠对饮食诱导的肥胖具有抗性。尽管在食物摄入量方面没有观察到差异,但敲除小鼠比其野生型对照更瘦。在呼吸交换率和产热方面没有观察到差异。然而,敲除小鼠比野生型同窝仔更活跃,这种活动水平可能是能量平衡差异的一个潜在原因。与野生型对照相比,突变小鼠对胰岛素更敏感,并且表现出改善的葡萄糖耐量。几种炎症标志物 MCP-1、CRP 和 IP-10 在突变动物中降低,表明 GPR21 也可能通过抗炎机制发挥其作用。我们发现 GPR21 在所有组织中广泛表达,在大脑和脾脏中表达水平最高。总的来说,这些发现表明 GPR21 可能在调节体重和葡萄糖代谢方面发挥重要作用。