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促性腺激素受体二聚化和寡聚化的分子及功能研究

Molecular and functional insights into gonadotropin hormone receptor dimerization and oligomerization.

作者信息

Agwuegbo Uche C, Jonas Kim C

机构信息

Vascular Biology Research Center, St George's University of London, London, UK.

Vascular Biology Research Center, St George's University of London, London, UK -

出版信息

Minerva Ginecol. 2018 Oct;70(5):539-548. doi: 10.23736/S0026-4784.18.04287-9. Epub 2018 Sep 13.

Abstract

The gonadotropin hormones, follicle stimulating hormone and luteinizing hormone, are essential for reproduction. They work in concert to control multiple aspects of gonadal function to ultimately produce meiotically competent and fertilizable gametes, provide the optimal endometrial environment and support for implantation and maintain pregnancy via progesterone production throughout the first trimester of pregnancy. These complex and multidimensional functions are mediated via the gonadotropin hormone receptors, luteinizing hormone receptor and follicle stimulating hormone receptor, Class A G protein-coupled receptors (GPCR), which couple to multiple G protein-dependent and independent signal pathways to control these physiological processes. Over the last two decades, a plethora of experimental evidence has shown that GPCRs can associate to form dimers and oligomers. This association provides a means of mediating the diverse functional requirements of a single receptor subtype and for the gonadotropin hormone receptors, has been shown to alter the pharmacology and signal activation profile of these receptors. This review will detail the historical and current evidence detailing the formation of gonadotropin hormone receptor homomers and heteromers. We will discuss the functional insights gained from in vitro and in vivo studies, and the potential impact in modulating reproductive health and disease.

摘要

促性腺激素,即卵泡刺激素和黄体生成素,对生殖至关重要。它们协同作用,控制性腺功能的多个方面,最终产生具有减数分裂能力和可受精的配子,提供最佳的子宫内膜环境,并通过在妊娠的前三个月产生孕酮来支持着床和维持妊娠。这些复杂的多维度功能是通过促性腺激素受体、黄体生成素受体和卵泡刺激素受体介导的,它们属于A类G蛋白偶联受体(GPCR),可与多种G蛋白依赖性和非依赖性信号通路偶联以控制这些生理过程。在过去二十年中,大量实验证据表明GPCR可以缔合形成二聚体和寡聚体。这种缔合提供了一种介导单一受体亚型的多种功能需求的方式,对于促性腺激素受体而言,已证明其可改变这些受体的药理学和信号激活特征。本综述将详细介绍有关促性腺激素受体同型二聚体和异型二聚体形成的历史和当前证据。我们将讨论从体外和体内研究中获得的功能见解,以及对调节生殖健康和疾病的潜在影响。

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