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膜受体:松弛素家族肽受体的结构与功能。

Membrane receptors: structure and function of the relaxin family peptide receptors.

机构信息

Florey Neuroscience Institutes, University of Melbourne, Victoria 3010, Australia.

出版信息

Mol Cell Endocrinol. 2010 May 14;320(1-2):1-15. doi: 10.1016/j.mce.2010.02.003. Epub 2010 Feb 6.

Abstract

The receptors for members of the relaxin peptide family have only recently been discovered and are G-protein-coupled receptors (GPCRs). Relaxin and insulin-like peptide 3 (INSL3) interact with the leucine-rich-repeat-containing GPCRs (LGRs) LGR7 and LGR8, respectively. These receptors show closest similarity to the glycoprotein hormone receptors and contain large ectodomains with 10 leucine-rich repeats (LRRs) but are unique members of the LGR family (class C) as they have an LDL class A (LDLa) module at their N-terminus. In contrast, relaxin-3 and INSL5 interact with another class of type I GPCRs which lack a large ectodomain, the peptide receptors GPCR135 and GPCR142, respectively. These receptors are now classified as relaxin family peptide (RXFP) receptors, RXFP1 (LGR7), RXFP2 (LGR8), RXFP3 (GPCR135) and RXFP4 (GPCR142). This review outlines the identification of the peptides and receptors, their expression profiles and physiological roles and the functional interactions of the peptides with their unique receptors.

摘要

松弛肽家族成员的受体最近才被发现,属于 G 蛋白偶联受体(GPCR)。松弛素和胰岛素样肽 3(INSL3)分别与富含亮氨酸重复序列的 GPCR(LGR)7 和 LGR8 相互作用。这些受体与糖蛋白激素受体最为相似,含有 10 个富含亮氨酸的重复序列(LRR)的大细胞外结构域,但它们是 LGR 家族(C 类)的独特成员,因为它们在 N 端具有 LDL 类 A(LDLa)模块。相比之下,松弛素 3 和 INSL5 分别与另一类缺乏大细胞外结构域的 I 型 GPCR 相互作用,即肽受体 GPCR135 和 GPCR142。这些受体现在被归类为松弛素家族肽(RXFP)受体,即 RXFP1(LGR7)、RXFP2(LGR8)、RXFP3(GPCR135)和 RXFP4(GPCR142)。这篇综述概述了肽和受体的鉴定、它们的表达谱和生理作用,以及肽与它们独特的受体的功能相互作用。

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