Zhao L, Bakke M, Parker K L
Division of Endocrinology, Department of Internal Medicine and Pharmacology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-8857, USA.
Mol Cell Endocrinol. 2001 Dec 20;185(1-2):27-32. doi: 10.1016/s0303-7207(01)00621-9.
Knockout mice lacking the orphan nuclear receptor steroidogenic factor 1 (SF-1) revealed its essential roles at multiple levels of endocrine development and function. These SF-1 knockout mice lacked adrenal glands and gonads, thereby manifesting adrenal insufficiency and sex reversal of their internal and external genitalia. Their pituitary gonadotropes failed to express several markers of normal differentiated function, and they lacked a specific hypothalamic nucleus, the ventromedial hypothalamic nucleus (VMH). Using the Cre-loxP system, we generated mice whose gene encoding SF-1 was inactivated specifically in the anterior pituitary. These pituitary-specific SF-1 knockout mice were sterile and never matured sexually. Their gonads weighed only approximately 5% of the weight of wild-type gonads. SF-1 immunoreactivity was absent in the anterior pituitary but was unaffected in the adrenal cortex, validating the selectivity of the gene targeting strategy. Consistent with an important role of SF-1 in gonadotropes, follicle-stimulating hormone (FSH) and luteinizing hormone (LH) were markedly decreased in the pituitary-specific SF-1 knockout mice. The pituitary-specific SF-1 knockout mice are a novel genetic model of hypogonadotropic hypogonadism and establish essential roles of SF-1 in gonadotropin expression.
缺乏孤儿核受体类固醇生成因子1(SF-1)的基因敲除小鼠揭示了其在内分泌发育和功能的多个层面上的重要作用。这些SF-1基因敲除小鼠缺乏肾上腺和性腺,从而表现出肾上腺功能不全以及内外生殖器的性反转。它们的垂体促性腺细胞无法表达正常分化功能的几种标志物,并且它们缺乏一个特定的下丘脑核团,即腹内侧下丘脑核(VMH)。利用Cre-loxP系统,我们构建了编码SF-1的基因在前脑垂体中特异性失活的小鼠。这些垂体特异性SF-1基因敲除小鼠不育且从未性成熟。它们的性腺重量仅约为野生型性腺重量的5%。前脑垂体中不存在SF-1免疫反应性,但肾上腺皮质中未受影响,这证实了基因靶向策略的选择性。与SF-1在促性腺细胞中的重要作用一致,垂体特异性SF-1基因敲除小鼠中的促卵泡激素(FSH)和促黄体生成素(LH)显著降低。垂体特异性SF-1基因敲除小鼠是一种新型的低促性腺激素性性腺功能减退的遗传模型,并确立了SF-1在促性腺激素表达中的重要作用。