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促性腺激素及其受体:协同进化、遗传变异、受体成像和功能拮抗剂。

Gonadotropins and their receptors: coevolution, genetic variants, receptor imaging, and functional antagonists.

机构信息

Program of Reproductive and Stem Cell Biology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, California, USA.

出版信息

Biol Reprod. 2018 Jul 1;99(1):3-12. doi: 10.1093/biolre/ioy012.

Abstract

Gonadotropins belong to the family of dimeric glycoprotein hormones and regulate gonadal physiology mediated by G protein-coupled, seven-transmembrane receptors. These glycoprotein hormones are widely used in the clinic to promote ovarian follicle development and for treating some cases of male infertility. We traced the coevolution of dimeric gonadotropin hormones and their receptors, together with thyrotropin and its receptor. We updated recent findings on human genetic variants of these genes and their association with dizygotic twining, polycystic ovarian syndrome, primary ovarian insufficiency, male-limited precocious puberty, and infertility. In addition to the known physiological roles of gonadotropin-receptor signaling in gonadal tissues, we also discussed emerging understanding of extragonadal functions of gonadotropins in bones and adipose tissues, together with recent advances in in vivo imaging of gonadotropin receptors in live animals. Recent development of gonadotropin receptor agonists and antagonists were summarized with an emphasis on the development of functional antagonists for FSH receptors to alleviate osteoporosis and obesity associated with menopause.

摘要

促性腺激素属于二聚糖蛋白激素家族,通过 G 蛋白偶联的七跨膜受体调节性腺生理学。这些糖蛋白激素在临床上被广泛用于促进卵泡发育和治疗某些男性不育症。我们追踪了二聚体促性腺激素及其受体与促甲状腺素及其受体的共同进化。我们更新了这些基因的人类遗传变异及其与双胎妊娠、多囊卵巢综合征、原发性卵巢功能不全、男性性早熟和不育症的关联的最新发现。除了促性腺激素-受体信号在性腺组织中的已知生理作用外,我们还讨论了促性腺激素在骨骼和脂肪组织中的性腺外功能的新认识,以及活体动物中促性腺激素受体的体内成像的最新进展。总结了促性腺激素受体激动剂和拮抗剂的最新发展,重点介绍了 FSH 受体功能性拮抗剂的开发,以缓解与绝经相关的骨质疏松症和肥胖症。

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