Steroidogenic factor 1: an essential mediator of endocrine development.

K. Parker, D. Rice, D. Lala, Y. Ikeda, Xunrong Luo, M. Wong, M. Bakke, Liping Zhao, C. Frigeri, N. Hanley, N. Stallings, B. Schimmer
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引用次数: 350

Abstract

The orphan nuclear receptor steroidogenic factor 1 (SF-1, also called Ad4BP and officially designated NR5A1) has emerged as an essential regulator of endocrine development and function. Initially identified as a tissue-specific transcriptional regulator of the cytochrome P450 steroid hydroxylases, SF-1 has considerably broader roles, as evidenced from studies in knockout mice lacking SF-1. The SF-1-knockout mice lacked adrenal glands and gonads and therefore died from adrenal insufficiency within the first week after birth. In addition, SF-1 knockout mice exhibited male-to-female sex reversal of their internal and external genitalia, impaired expression of multiple markers of pituitary gonadotropes, and agenesis of the ventromedial hypothalamic nucleus (VMH). These studies delineated essential roles of SF-I in regulating endocrine differentiation and function at multiple levels, particularly with respect to reproduction. This chapter will review the experiments that established SF-1 as a pivotal, global determinant of endocrine differentiation and function. We next discuss recent insights into the mechanisms controlling the expression and function of SF-1 as well as the current status of research aimed at delineating its roles in specific tissues. Finally, we highlight areas where additional studies are needed to expand our understanding of SF-1 action.
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甾体生成因子1:内分泌发育的重要介质。
孤儿核受体甾体生成因子1 (SF-1,也称为Ad4BP,正式命名为NR5A1)已成为内分泌发育和功能的重要调节因子。SF-1最初被认为是细胞色素P450类固醇羟化酶的组织特异性转录调节剂,从缺乏SF-1的敲除小鼠的研究中可以证明,SF-1具有相当广泛的作用。sf -1基因敲除小鼠缺乏肾上腺和性腺,因此在出生后的第一周内死于肾上腺功能不全。此外,SF-1基因敲除小鼠表现出雌雄外生殖器性别逆转,垂体促性腺激素的多种标记物表达受损,下丘脑腹内侧核(VMH)发育不全。这些研究描述了sf - 1在多个水平上调节内分泌分化和功能的重要作用,特别是在生殖方面。本章将回顾建立SF-1作为内分泌分化和功能的关键、全局决定因素的实验。接下来,我们将讨论最近对SF-1表达和功能控制机制的见解,以及旨在描述其在特定组织中的作用的研究现状。最后,我们强调了需要进一步研究的领域,以扩大我们对SF-1作用的理解。
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