Bueschbell Beatriz, Manga Prashiela, Schiedel Anke C
Department of Pharmaceutical and Medicinal Chemistry, Pharmaceutical Institute, University of Bonn, Bonn, Germany.
Ronald O. Perelman Department of Dermatology, Grossman School of Medicine, New York University, New York City, NY, United States.
Front Mol Biosci. 2022 Apr 12;9:873777. doi: 10.3389/fmolb.2022.873777. eCollection 2022.
GPCRs transform extracellular stimuli into a physiological response by activating an intracellular signaling cascade initiated via binding to G proteins. Orphan G protein-coupled receptors (GPCRs) hold the potential to pave the way for development of new, innovative therapeutic strategies. In this review we will introduce G protein-coupled receptor 143 (GPR143), an enigmatic receptor in terms of classification within the GPCR superfamily and localization. GPR143 has not been assigned to any of the GPCR families due to the lack of common structural motifs. Hence we will describe the most important motifs of classes A and B and compare them to the protein sequence of GPR143. While a precise function for the receptor has yet to be determined, the protein is expressed abundantly in pigment producing cells. Many GPR143 mutations cause X-linked Ocular Albinism Type 1 (OA1, Nettleship-Falls OA), which results in hypopigmentation of the eyes and loss of visual acuity due to disrupted visual system development and function. In pigment cells of the skin, loss of functional GPR143 results in abnormally large melanosomes (organelles in which pigment is produced). Studies have shown that the receptor is localized internally, including at the melanosomal membrane, where it may function to regulate melanosome size and/or facilitate protein trafficking to the melanosome through the endolysosomal system. Numerous additional roles have been proposed for GPR143 in determining cancer predisposition, regulation of blood pressure, development of macular degeneration and signaling in the brain, which we will briefly describe as well as potential ligands that have been identified. Furthermore, GPR143 is a promiscuous receptor that has been shown to interact with multiple other melanosomal proteins and GPCRs, which strongly suggests that this orphan receptor is likely involved in many different physiological actions.
G蛋白偶联受体(GPCRs)通过激活经由与G蛋白结合而启动的细胞内信号级联反应,将细胞外刺激转化为生理反应。孤儿G蛋白偶联受体(GPCRs)有可能为新的创新治疗策略的开发铺平道路。在这篇综述中,我们将介绍G蛋白偶联受体143(GPR143),它在GPCR超家族中的分类和定位方面是一个神秘的受体。由于缺乏共同的结构基序,GPR143尚未被归入任何GPCR家族。因此,我们将描述A类和B类的最重要基序,并将它们与GPR143的蛋白质序列进行比较。虽然该受体的确切功能尚未确定,但该蛋白在色素生成细胞中大量表达。许多GPR143突变会导致X连锁1型眼白化病(OA1,内特尔希普-福尔斯眼白化病),由于视觉系统发育和功能紊乱,会导致眼睛色素减退和视力丧失。在皮肤的色素细胞中,功能性GPR143的缺失会导致异常大的黑素体(产生色素的细胞器)。研究表明,该受体定位于细胞内部,包括黑素体膜,在那里它可能起到调节黑素体大小和/或促进蛋白质通过内溶酶体系统运输到黑素体的作用。对于GPR143在确定癌症易感性、血压调节、黄斑变性发展和大脑信号传导方面,还提出了许多其他作用,我们将简要描述以及已鉴定的潜在配体。此外,GPR143是一种杂乱的受体,已被证明与多种其他黑素体蛋白和GPCR相互作用,这强烈表明这种孤儿受体可能参与许多不同的生理作用。