Department of Surgery, Yale School of Medicine, New Haven, Connecticut;
INSERM UMR_S1138, Paris, France; Paris Descartes University, Paris, France; Assistance Publique-Hopitaux de Paris, Hopital Europeen Georges Pompidou, Paris, France.
Am J Physiol Cell Physiol. 2014 Aug 1;307(3):C221-31. doi: 10.1152/ajpcell.00139.2014. Epub 2014 May 28.
The calcium-sensing receptor (CaSR) has played an important role as a target in the treatment of a variety of disease states over the past 20 plus years. In this review, we give an overview of the receptor at the cellular level and then provide details as to how this receptor has been targeted to modulate cellular ion transport mechanisms. As a member of the G protein-coupled receptor (GPCR) family, it has a high degree of homology with a variety of other members in this class, which could explain why this receptor has been identified in so many different tissues throughout the body. This diversity of locations sets it apart from other members of the family and may explain how the receptor interacts with so many different organ systems in the body to modulate the physiology and pathophysiology. The receptor is unique in that it has two large exofacial lobes that sit in the extracellular environment and sense changes in a wide variety of environmental cues including salinity, pH, amino acid concentration, and polyamines to name just a few. It is for this reason that there has been a great deal of research associated with normal receptor physiology over the past 20 years. With the ongoing research, in more recent years a focus on the pathophysiology has emerged and the effects of receptor mutations on cellular and organ physiology have been identified. We hope that this review will enhance and update the knowledge about the importance of this receptor and stimulate future potential investigations focused around this receptor in cellular, organ, and systemic physiology and pathophysiology.
在过去的 20 多年里,钙敏感受体 (CaSR) 作为治疗多种疾病状态的靶点发挥了重要作用。在这篇综述中,我们首先概述了细胞水平上的受体,然后详细介绍了如何针对该受体来调节细胞离子转运机制。作为 G 蛋白偶联受体 (GPCR) 家族的一员,它与该家族的许多其他成员具有高度同源性,这可以解释为什么该受体在体内的许多不同组织中都有发现。这种多样性的分布使它有别于其他家族成员,并可能解释了该受体如何与体内如此多的不同器官系统相互作用,从而调节生理和病理生理。该受体的独特之处在于它有两个位于细胞外环境中的大型细胞外裂片,能够感知多种环境信号的变化,包括盐度、pH 值、氨基酸浓度、多胺等。正是由于这个原因,在过去的 20 年里,围绕着该受体的正常受体生理学开展了大量的研究。随着研究的不断深入,近年来,人们对该受体的病理生理学越来越关注,已经确定了受体突变对细胞和器官生理学的影响。我们希望这篇综述能增强和更新对该受体重要性的认识,并激发未来围绕该受体在细胞、器官和全身生理学及病理生理学方面的潜在研究。