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甲状旁腺激素受体-1信号传导——作用机制见解与治疗前景

PTH receptor-1 signalling-mechanistic insights and therapeutic prospects.

作者信息

Cheloha Ross W, Gellman Samuel H, Vilardaga Jean-Pierre, Gardella Thomas J

机构信息

Department of Chemistry, 1101 University Avenue, University of Wisconsin, Madison, WI 53706, USA.

Laboratory for GPCR Biology, Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, 200 Lothrop Street, Pittsburgh, PA 15213, USA.

出版信息

Nat Rev Endocrinol. 2015 Dec;11(12):712-24. doi: 10.1038/nrendo.2015.139. Epub 2015 Aug 25.

Abstract

Parathyroid hormone/parathyroid hormone-related protein receptor (PTH/PTHrP type 1 receptor; commonly known as PTHR1) is a family B G-protein-coupled receptor (GPCR) that regulates skeletal development, bone turnover and mineral ion homeostasis. PTHR1 transduces stimuli from PTH and PTHrP into the interior of target cells to promote diverse biochemical responses. Evaluation of the signalling properties of structurally modified PTHR1 ligands has helped to elucidate determinants of receptor function and mechanisms of downstream cellular and physiological responses. Analysis of PTHR1 responses induced by structurally modified ligands suggests that PTHR1 can continue to signal through a G-protein-mediated pathway within endosomes. Such findings challenge the longstanding paradigm in GPCR biology that the receptor is transiently activated at the cell membrane, followed by rapid deactivation and receptor internalization. Evaluation of structurally modified PTHR1 ligands has further led to the identification of ligand analogues that differ from PTH or PTHrP in the type, strength and duration of responses induced at the receptor, cellular and organism levels. These modified ligands, and the biochemical principles revealed through their use, might facilitate an improved understanding of PTHR1 function in vivo and enable the treatment of disorders resulting from defects in PTHR1 signalling. This Review discusses current understanding of PTHR1 modes of action and how these findings might be applied in future therapeutic agents.

摘要

甲状旁腺激素/甲状旁腺激素相关蛋白受体(PTH/PTHrP 1型受体;通常称为PTHR1)是一种B类G蛋白偶联受体(GPCR),可调节骨骼发育、骨转换和矿物质离子稳态。PTHR1将来自PTH和PTHrP的刺激传导至靶细胞内部,以促进多种生化反应。对结构修饰的PTHR1配体的信号特性进行评估,有助于阐明受体功能的决定因素以及下游细胞和生理反应的机制。对结构修饰配体诱导的PTHR1反应的分析表明,PTHR1可以在内体中通过G蛋白介导的途径继续发出信号。这些发现挑战了GPCR生物学中由来已久的范式,即受体在细胞膜上被短暂激活,随后迅速失活并发生受体内化。对结构修饰的PTHR1配体的评估还导致了配体类似物的鉴定,这些类似物在受体、细胞和生物体水平上诱导的反应类型、强度和持续时间与PTH或PTHrP不同。这些修饰的配体以及通过使用它们所揭示的生化原理,可能有助于更好地理解PTHR1在体内的功能,并能够治疗由PTHR1信号缺陷引起的疾病。本综述讨论了目前对PTHR1作用模式的理解,以及这些发现如何应用于未来的治疗药物。

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