生物
类固醇生成因子1
内分泌学
内科学
促性腺细胞
基因剔除小鼠
垂体
激素
核受体
受体
转录因子
遗传学
医学
基因
作者
Liping Zhao,Marit Bakke,Yelena Krimkevich,Lisa J. Cushman,Albert F. Parlow,Sally A. Camper,Keith L. Parker
出处
期刊:Development
[The Company of Biologists]
日期:2001-01-15
卷期号:128 (2): 147-154
被引量:223
标识
DOI:10.1242/dev.128.2.147
摘要
ABSTRACT Knockout mice lacking the orphan nuclear receptor steroidogenic factor 1 (SF1) exhibit a complex endocrine phenotype that includes adrenal and gonadal agenesis, impaired expression of pituitary gonadotropins, and absence of the ventromedial hypothalamic nucleus (VMH). These multiple defects complicate efforts to delineate primary versus secondary effects of SF1 deficiency in different tissues, such that its direct role in gonadotropes remains uncertain. To define this role, we have expressed Cre recombinase driven by the promoter region of the common α subunit of glycoprotein hormones (αGSU), thereby inactivating a loxP-modified SF1 locus in the anterior pituitary gland. Although pituitary-specific SF1 knockout mice were fully viable, they were sterile and failed to develop normal secondary sexual characteristics. Their adrenal glands and VMH appeared normal histologically, but their testes and ovaries were severely hypoplastic. αGSU-Cre, loxP mice had normal levels of most pituitary hormones, but had markedly decreased expression of LH and FSH. Treatment with exogenous gonadotropins stimulated gonadal steroidogenesis, inducing germ cell maturation in males and follicular and uterine maturation in females – establishing that the gonads can respond to gonadotropins. The pituitary-specific SF1 knockout mice are a novel genetic model of hypogonadotropic hypogonadism that establishes essential role(s) of SF1 in pituitary gonadotropes.
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