Department of Endocrinology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
Department of Endocrinology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
Prog Mol Biol Transl Sci. 2019;161:69-89. doi: 10.1016/bs.pmbts.2018.09.007. Epub 2018 Nov 23.
Accumulating evidence showed that the luteinizing hormone/chorionic gonadotropin receptor (LHCGR) is an essential regulator of sexual development and reproduction from zebrafish to human. Activating and inactivating mutations of LHCGR gene have been identified from patients of different phenotypes. Familial male-limited precocious puberty, Leydig cell hypoplasia, and empty follicle syndrome are caused by LHCGR mutations. More than 50 mutations have been reported from subjects of different ethnic backgrounds. Functional analyses of the mutant LHCGR revealed multiple defects, including cell surface expression, ligand binding, and signaling. The difference of the two native ligands and signaling pathway activated by LHCGR are illustrated. Potential therapeutic implications from the analyses of the naturally occurring LHCGR mutations, such as pharmacological chaperones, are highlighted.
越来越多的证据表明,从斑马鱼到人,促黄体生成素/绒毛膜促性腺激素受体(LHCGR)是性发育和生殖的重要调节剂。已经从不同表型的患者中鉴定出 LHCGR 基因的激活和失活突变。LHCGR 突变可导致家族性男性限性性早熟、睾丸间质细胞发育不全和空卵泡综合征。来自不同种族背景的受试者已报告了 50 多种突变。对突变 LHCGR 的功能分析显示出多种缺陷,包括细胞表面表达、配体结合和信号转导。本文阐述了两种天然配体和 LHCGR 激活的信号通路的差异。从对天然 LHCGR 突变的分析中得出了一些潜在的治疗意义,例如药理学伴侣。