Miyauchi Satoshi, Hirasawa Akira, Iga Tomoyo, Liu Ning, Itsubo Chisato, Sadakane Keiko, Hara Takafumi, Tsujimoto Gozoh
Graduate School of Pharmaceutical Science, Kyoto University, 46-29 Yoshida-Shimoadachi-machi, Sakyo-ku, Kyoto, Kyoto, 606-8501, Japan.
Naunyn Schmiedebergs Arch Pharmacol. 2009 Apr;379(4):427-34. doi: 10.1007/s00210-008-0390-8. Epub 2009 Jan 15.
GPR120 is a G-protein-coupled receptor whose endogenous ligands have recently been identified as free fatty acids. It has been implicated as playing an important role in the control of lipid and glucose metabolism by regulating the secretion of glucagon-like peptide-1 and cholecystokinin. We have developed an antibody against the extracellular domain of GPR120. The specificity of the antibody was demonstrated by immunoprecipitation, Western blotting, flow cytometry, and immunocytochemistry using GPR120-transfected cells. Immunoreactivity for GPR120 was abundant in the mouse large intestine, lung, and adipose tissue. Furthermore, we found that the expression of GPR120 protein was up-regulated during the adipogenic differentiation of 3T3-L1 cells, which corresponded well with changes in mRNA expression. The anti-GPR120 antibody will be of value for the further study of the function of this nutrient-sensing receptor.
GPR120是一种G蛋白偶联受体,其内源性配体最近被确定为游离脂肪酸。它通过调节胰高血糖素样肽-1和胆囊收缩素的分泌,在脂质和葡萄糖代谢的控制中发挥重要作用。我们已经开发出一种针对GPR120细胞外结构域的抗体。使用GPR120转染细胞,通过免疫沉淀、蛋白质印迹、流式细胞术和免疫细胞化学证明了该抗体的特异性。GPR120的免疫反应性在小鼠大肠、肺和脂肪组织中丰富。此外,我们发现GPR120蛋白的表达在3T3-L1细胞成脂分化过程中上调,这与mRNA表达的变化非常吻合。抗GPR120抗体将对进一步研究这种营养感应受体的功能具有重要价值。