Huhtaniemi Ilpo, Ahtiainen Petteri, Pakarainen Tomi, Rulli Susana B, Zhang Fu-Ping, Poutanen Matti
Institute of Reproductive and Developmental Biology, Hammersmith Campus, Imperial College London, Du Cane Road, London W12 0NN, UK.
Mol Cell Endocrinol. 2006 Jun 27;252(1-2):126-35. doi: 10.1016/j.mce.2006.03.026. Epub 2006 May 3.
Numerous genetically modified mouse models have recently been developed for the study of the pituitary-gonadal interactions. They include spontaneous or engineered knockouts (KO) of the gonadotrophin-releasing hormone (GnRH) and its receptor, the gonadotrophin common-alpha(Calpha), luteinising hormone (LH) beta and follicle-stimulating hormone (FSH) beta subunits, and the two gonadotrophin receptors (R), LHR and FSHR. In addition, there are also transgenic (TG) mice overexpressing gonadotrophin subunits and producing supraphysiological levels of these hormones. These models have offered relevant phenocopies for similar mutations in humans and to a great extent expanded our knowledge on normal and pathological functions of the hypothalamic-pituitary-gonadal (HPG) axis. The purpose of this article is to review some of our recent findings on two such mouse models, the LHR KO mouse (LuRKO), and the hCG overexpressing TG mouse (hCG+).
最近已开发出许多转基因小鼠模型用于研究垂体 - 性腺相互作用。它们包括促性腺激素释放激素(GnRH)及其受体、促性腺激素共同α亚基(Cα)、黄体生成素(LH)β亚基和卵泡刺激素(FSH)β亚基以及两种促性腺激素受体(R),即促黄体生成素受体(LHR)和促卵泡激素受体(FSHR)的自发或工程敲除(KO)小鼠。此外,还有过表达促性腺激素亚基并产生超生理水平这些激素的转基因(TG)小鼠。这些模型为人类的类似突变提供了相关的表型模拟,并在很大程度上扩展了我们对下丘脑 - 垂体 - 性腺(HPG)轴正常和病理功能的认识。本文的目的是综述我们最近在两种这样的小鼠模型上的一些发现,即促黄体生成素受体敲除小鼠(LuRKO)和过表达人绒毛膜促性腺激素的转基因小鼠(hCG +)。