Molecular Biology Program, Faculty of Medicine, Université de Montréal, Montreal, Quebec, Canada.
Research Center of Centre Hospitalier Universitaire Sainte-Justine, Montreal, Quebec, Canada.
Am J Physiol Cell Physiol. 2023 Dec 1;325(6):C1502-C1515. doi: 10.1152/ajpcell.00346.2023. Epub 2023 Oct 30.
G-coupled protein receptors (GPCRs) are the ultimate refuge of pharmacology and medicine as more than 40% of all marketed drugs are directly targeting these receptors. Through cell surface expression, they are at the forefront of cellular communication with the outside world. Metabolites among the conveyors of this communication are becoming more prominent with the recognition of them as ligands for GPCRs. HCAR1 is a GPCR conveyor of lactate. It is a class A GPCR coupled to G which reduces cellular cAMP along with the downstream G signaling. It was first found to inhibit lipolysis, and lately has been implicated in diverse cellular processes, including neural activities, angiogenesis, inflammation, vision, cardiovascular function, stem cell proliferation, and involved in promoting pathogenesis for different conditions, such as cancer. Other than signaling from the plasma membrane, HCAR1 shows nuclear localization with different location-biased activities therein. Although different functions for HCAR1 are being discovered, its cell and molecular mechanisms are yet ill understood. Here, we provide a comprehensive review on HCAR1, which covers the literature on the subject, and discusses its importance and relevance in various biological phenomena.
G 蛋白偶联受体(GPCRs)是药理学和医学的终极研究目标,因为超过 40%的上市药物直接针对这些受体。通过细胞表面表达,它们处于细胞与外界通讯的最前沿。随着人们认识到代谢物是 GPCR 的配体,它们作为通讯载体的作用越来越突出。HCAR1 是一种 GPCR 传递的乳酸盐。它是一种与 G 偶联的 A 类 GPCR,可降低细胞内 cAMP 以及下游 G 信号转导。它最初被发现抑制脂肪分解,最近已被牵涉到多种细胞过程,包括神经活动、血管生成、炎症、视力、心血管功能、干细胞增殖,并参与促进不同疾病的发病机制,如癌症。除了来自质膜的信号外,HCAR1 还显示出核定位,并在其中具有不同位置偏向的活性。尽管正在发现 HCAR1 的不同功能,但对其细胞和分子机制仍知之甚少。在这里,我们提供了对 HCAR1 的全面综述,涵盖了该主题的文献,并讨论了它在各种生物现象中的重要性和相关性。