Tremblay Frédéric, Perreault Mylène, Klaman Lori D, Tobin James F, Smith Erica, Gimeno Ruth E
Cardiovascular and Metabolic Diseases, Wyeth Research, 200 Cambridge Park Drive (T4007E), Cambridge, Massachusetts 02140, USA.
Endocrinology. 2007 Feb;148(2):501-6. doi: 10.1210/en.2006-1275. Epub 2006 Nov 9.
It has been recently proposed that obestatin, a peptide encoded by the ghrelin gene, reduces food intake by activating the orphan G protein-coupled receptor GPR39. To gain further insights into the role of GPR39 in body weight homeostasis, we characterized the phenotype of mice with targeted disruption of the GPR39 gene. Body weight, adiposity, and food intake were found to be similar between GPR39(+/+) and GPR39(-/-) mice. Furthermore, fasting glucose and insulin levels were similar between both genotypes. Injection of obestatin peptide (1 micromol/kg, ip) obtained from multiple sources did not consistently inhibit food intake in wild-type mice after an overnight fast, and no difference in food intake was observed between wild-type and GPR39 knockout mice after injection of the peptide. Finally, ectopic expression of GPR39 in HEK293T cells revealed a constitutive activation of the receptor that was unaffected by stimulation with obestatin. Our phenotypic characterization suggests that GPR39 is not a major modulator of food intake in mice, although a more subtle role cannot be excluded. The role of GPR39 in normal physiology requires further study and should be conducted independently of the function of obestatin.
最近有人提出,胃饥饿素基因编码的一种肽——肥胖抑制素,通过激活孤儿G蛋白偶联受体GPR39来减少食物摄入量。为了进一步深入了解GPR39在体重稳态中的作用,我们对GPR39基因靶向破坏的小鼠的表型进行了特征分析。发现GPR39(+/+)和GPR39(-/-)小鼠之间的体重、肥胖程度和食物摄入量相似。此外,两种基因型之间的空腹血糖和胰岛素水平也相似。从多个来源获得的肥胖抑制素肽(1微摩尔/千克,腹腔注射)在过夜禁食后并不能持续抑制野生型小鼠的食物摄入量,注射该肽后野生型小鼠和GPR39基因敲除小鼠之间的食物摄入量没有差异。最后,GPR39在HEK293T细胞中的异位表达显示该受体存在组成性激活,且不受肥胖抑制素刺激的影响。我们的表型特征分析表明,GPR39不是小鼠食物摄入量的主要调节因子,尽管不能排除其有更微妙的作用。GPR39在正常生理学中的作用需要进一步研究,且应独立于肥胖抑制素的功能进行研究。