Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA.
Mol Cell Endocrinol. 2010 Nov 25;329(1-2):47-55. doi: 10.1016/j.mce.2010.04.025. Epub 2010 May 2.
The luteinizing hormone receptor (LHR), one of the three glycoprotein hormone receptors, is necessary for critical reproductive processes, including gonadal steroidogenesis, oocyte maturation and ovulation, and male sex differentiation. Moreover, it has been postulated to contribute to certain neoplasms, particularly ovarian cancer. A member of the G protein-coupled receptor family, LHR contains a relatively large extracellular domain responsible for high affinity hormone binding; transmembrane activation then leads to G protein coupling and subsequent second messenger production. This review deals with recent advances in our understanding of LHR structure and structure-function relationships, as well as hormone-mediated changes in gene expression in ovarian cancer cells expressing LHR. Suggestions are also made for critical gaps that need to be filled as the field advances, including determination of the three-dimensional structure of inactive and active receptor, elucidation of the mechanism by which hormone binding to the extracellular domain triggers the activation of Gs, clarification of the putative roles of LHR in non-gonadal tissues, and the role, if any, of activated receptor in the development or progression of ovarian cancer.
黄体生成素受体(LHR)是三种糖蛋白激素受体之一,对于包括性腺类固醇生成、卵母细胞成熟和排卵以及男性性别分化在内的关键生殖过程是必需的。此外,它被认为与某些肿瘤有关,特别是卵巢癌。LHR 是 G 蛋白偶联受体家族的成员,它包含一个相对较大的细胞外结构域,负责与激素的高亲和力结合;然后通过跨膜激活导致 G 蛋白偶联和随后的第二信使产生。这篇综述涉及我们对 LHR 结构和结构-功能关系的最新认识,以及在表达 LHR 的卵巢癌细胞中激素介导的基因表达变化。还提出了该领域前进时需要解决的关键空白,包括确定无活性和活性受体的三维结构、阐明激素与细胞外结构域结合触发 Gs 激活的机制、阐明 LHR 在非性腺组织中的潜在作用,以及如果有的话,激活的受体在卵巢癌的发展或进展中的作用。