Guo Cong, Chen Wei-Dong, Wang Yan-Dong
State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology Beijing, China.
Key Laboratory of Receptors-Mediated Gene Regulation and Drug Discovery, School of Medicine, Henan UniversityKaifeng, China; Key Laboratory of Molecular Pathology, School of Basic Medical Science, Inner Mongolia Medical UniversityHohhot, China.
Front Physiol. 2016 Dec 26;7:646. doi: 10.3389/fphys.2016.00646. eCollection 2016.
G-protein-coupled bile acid receptor, Gpbar1 (TGR5), is a member of G-protein-coupled receptor (GPCR) superfamily. High levels of TGR5 mRNA were detected in several tissues such as small intestine, stomach, liver, lung, especially in placenta and spleen. TGR5 is not only the receptor for bile acids, but also the receptor for multiple selective synthetic agonists such as 6α-ethyl-23(S)-methyl-cholic acid (6-EMCA, INT-777) and a series of 4-benzofuranyloxynicotinamde derivatives to regulate different signaling pathways such as nuclear factor κB (NF-κB), AKT, and extracellular signal-regulated kinases (ERK). TGR5, as a metabolic regulator, is involved in energy homeostasis, bile acid homeostasis, as well as glucose metabolism. More recently, our group and others have extended the functions of TGR5 to more than metabolic regulation, which include inflammatory response, cancer and liver regeneration. These findings highlight TGR5 as a potential drug target for different diseases. This review summarizes the basic information of TGR5 and its new functions.
G蛋白偶联胆汁酸受体Gpbar1(TGR5)是G蛋白偶联受体(GPCR)超家族的成员。在小肠、胃、肝脏、肺等多种组织中检测到高水平的TGR5 mRNA,尤其是在胎盘和脾脏中。TGR5不仅是胆汁酸的受体,也是多种选择性合成激动剂的受体,如6α-乙基-23(S)-甲基胆酸(6-EMCA,INT-777)和一系列4-苯并呋喃基氧基烟酰胺衍生物,可调节不同的信号通路,如核因子κB(NF-κB)、AKT和细胞外信号调节激酶(ERK)。TGR5作为一种代谢调节因子,参与能量稳态、胆汁酸稳态以及葡萄糖代谢。最近,我们团队和其他团队将TGR5的功能扩展到了代谢调节之外,包括炎症反应、癌症和肝脏再生。这些发现突出了TGR5作为不同疾病潜在药物靶点的地位。本综述总结了TGR5的基本信息及其新功能。