Robas Nicola, Mead Emma, Fidock Mark
Department of Target Genomics, Pfizer Global Research and Development, Sandwich, Kent, CT13 N9J, United Kingdom.
J Biol Chem. 2003 Nov 7;278(45):44400-4. doi: 10.1074/jbc.M302456200. Epub 2003 Aug 12.
MrgX2 is a recently identified orphan G-protein-coupled receptor whose ligand and physiological function were unknown. Here we describe cortistatin, a neuropeptide for which no specific receptor has been identified previously, as a high potency ligand at MrgX2. Cortistatin has several biological functions including roles in sleep regulation, locomotor activity, and cortical function. Using a "reverse pharmacology" approach, we have identified a number of additional cyclic peptide agonists for MrgX2, determined their rank order of potency, and demonstrated that this receptor has a pharmacological profile distinct from the other characterized members of the Mrg (Mas-related genes) family. In MrgX2-expressing cells, cortistatin-stimulated increases in intracellular Ca2+ but had no effect on basal or forskolin-stimulated cAMP levels, suggesting that this receptor is Gq-coupled. Immunohistochemical and quantitative PCR studies show MrgX2 to have a limited expression profile, both peripheral and within the central nervous system, with highest levels in dorsal root ganglion.
MrgX2是一种最近发现的孤儿G蛋白偶联受体,其配体和生理功能尚不清楚。在此,我们描述了促皮质素,一种此前未鉴定出特异性受体的神经肽,它是MrgX2的高效配体。促皮质素具有多种生物学功能,包括在睡眠调节、运动活动和皮质功能方面发挥作用。通过“反向药理学”方法,我们鉴定出了多种MrgX2的环肽激动剂,确定了它们的效价顺序,并证明该受体具有与Mrg(Mas相关基因)家族其他已鉴定成员不同的药理学特征。在表达MrgX2的细胞中,促皮质素刺激细胞内Ca2+增加,但对基础或福斯可林刺激的cAMP水平没有影响,这表明该受体与Gq偶联。免疫组织化学和定量PCR研究表明,MrgX2在外周和中枢神经系统中的表达谱有限,在背根神经节中水平最高。