Expression of LRH-1 and SF-1 in the mouse ovary: localization in different cell types correlates with differing function

被引:130
作者
Hinshelwood, MM
Repa, JJ
Shelton, JM
Richardson, JA
Mangelsdorf, DJ
Mendelson, CR
机构
[1] Univ Texas, SW Med Ctr, Dept Biochem, Dallas, TX 75390 USA
[2] Univ Texas, SW Med Ctr, Dept Obstet & Gynecol, Dallas, TX 75390 USA
[3] Univ Texas, SW Med Ctr, Dept Physiol & Internal Med, Dallas, TX 75390 USA
[4] Univ Texas, SW Med Ctr, Dept Internal Med, Div Cardiol, Dallas, TX 75390 USA
[5] Univ Texas, SW Med Ctr, Dept Pathol & Mol Biol, Dallas, TX 75390 USA
[6] Univ Texas, SW Med Ctr, Dept Pharmacol, Dallas, TX 75390 USA
[7] Univ Texas, SW Med Ctr, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
LRH-1; SF-1; aromatase; ovary; granulosa; cell; luteal cell;
D O I
10.1016/S0303-7207(03)00257-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Steroid biosynthesis in ovary is enhanced by the orphan nuclear receptor, steroidogenic factor-1 (SF-1); however, we reported that liver receptor homolog-1 (LRH-1), a closely related receptor to SF-1, is also expressed in mouse ovary. To further investigate the role of LRH-1 in mouse ovary, we used in situ hybridization to identify the cell types that express LRH-1 versus SF-1, and carried out functional studies to determine the role of LRH-1 in the regulation of the human (h) ovary-specific CYP19 promoter. LRH-1 expression was found to be abundant and highly restricted to cells involved in estrogen biosynthesis-granulosa cells during the estrous cycle, and in corpora lutea (CL) of pregnancy. In contrast, SF-1 was expressed most highly in C-19-steroid-producing theca cells and interstitium, and at low levels in granulosa and luteal cells. Transfection studies using gramilosa cells demonstrated that LRH-1 is a potent regulator of both basal and forskolin-induced transcription of the ovary-specific hCYP19 promoter. This activity was dependent upon two nuclear receptor half-sites within the proximal hCYP19 promoter. Based on these findings, we propose that LRH-1 plays an important role as a competence factor in regulating aromatase, and thus estrogen biosynthesis, in ovary. (C) 2003 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:39 / 45
页数:7
相关论文
共 30 条
[21]   CPF:: An orphan nuclear receptor that regulates liver-specific expression of the human cholesterol 7α-hydroxylase gene [J].
Nitta, M ;
Ku, S ;
Brown, C ;
Okamoto, AY ;
Shan, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6660-6665
[22]   The mouse fetoprotein transcription factor (FTF) gene promoter is regulated by three GATA elements with tandem E box and Nkx motifs, and FTF in turn activates the Hnf3β, Hnf4α, and Hnf1α gene promoters [J].
Paré, JF ;
Roy, S ;
Galarneau, L ;
Bélanger, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :13136-13144
[23]   Nuclear receptor regulation of cholesterol and bile acid metabolism [J].
Repa, JJ ;
Mangelsdorf, DJ .
CURRENT OPINION IN BIOTECHNOLOGY, 1999, 10 (06) :557-563
[24]   The role of orphan nuclear receptors in the regulation of cholesterol homeostasis [J].
Repa, JJ ;
Mangelsdorf, DJ .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2000, 16 :459-481
[25]  
RICHARDS J S, 1987, Steroids, V50, P393, DOI 10.1016/0039-128X(87)90027-4
[26]  
Shelton JM, 2000, J LIPID RES, V41, P532
[27]   Liver receptor homologue-1 is expressed in human steroidogenic tissues and activates transcription of genes encoding steroidogenic enzymes [J].
Sirianni, R ;
Seely, JB ;
Attia, G ;
Stocco, DM ;
Carr, BR ;
Pezzi, V ;
Rainey, WE .
JOURNAL OF ENDOCRINOLOGY, 2002, 174 (03) :R13-R17
[28]   REGULATION BY FOLLICLE-STIMULATING-HORMONE OF THE SYNTHESIS OF AROMATASE CYTOCHROME-P-450 IN HUMAN GRANULOSA-CELLS [J].
STEINKAMPF, MP ;
MENDELSON, CR ;
SIMPSON, ER .
MOLECULAR ENDOCRINOLOGY, 1987, 1 (07) :465-471
[29]   INVIVO AND INVITRO OVARIAN STEROIDOGENESIS IN THE PREGNANT RAT [J].
TAYA, K ;
GREENWALD, GS .
BIOLOGY OF REPRODUCTION, 1981, 25 (04) :683-691
[30]   GATA factors differentially activate multiple gonadal promoters through conserved GATA regulatory elements [J].
Tremblay, JJ ;
Viger, RS .
ENDOCRINOLOGY, 2001, 142 (03) :977-986