Thyroid hormone, retinoic acid, and testosterone suppress proliferation and induce markers of differentiation in cultured rat Sertoli cells

被引:108
作者
Buzzard, JJ
Wreford, NG
Morrison, JR
机构
[1] Monash Univ, Monash Inst Reprod & Dev, Clayton, Vic 3168, Australia
[2] Monash Univ, Dept Anat & Cell Biol, Clayton, Vic 3168, Australia
关键词
D O I
10.1210/en.2003-0379
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study uses a high purity cell culture system to extend previous observations of factors controlling the end of the Sertoli cell proliferative phase. Thyroid hormone, retinoic acid, and testosterone were assessed for their ability to halt the proliferative phase and regulate the expression of markers associated with maturation of the Sertoli cell. We show that these hormones share similar suppressive effects on the rate of Sertoli cell division without any apparent additive effects. We demonstrate that these hormones induce the progressive accumulation of cell cycle inhibitors p27Kip1 and p21Cip1 in Sertoli cells, a likely regulatory mechanism controlling the suppression of proliferation. We used real-time RT-PCR to examine the effects of these factors on the expression of mRNA encoding the Id proteins, demonstrating an increase in Id2 and Id3 expression in Sertoli cells treated with thyroid hormone, retinoic acid, or testosterone. Finally, we examined the expression of a number of genes that have been implicated in the Sertoli cell differentiation process. Our results suggest that these hormones can induce aspects of Sertoli cell differentiation in vitro, providing a valuable in vitro model for studying Sertoli cell function.
引用
收藏
页码:3722 / 3731
页数:10
相关论文
共 71 条
[21]   MICE LACKING P21(C/P1/WAF1) UNDERGO NORMAL DEVELOPMENT, BUT ARE DEFECTIVE IN G1 CHECKPOINT CONTROL [J].
DENG, CX ;
ZHANG, PM ;
HARPER, JW ;
ELLEDGE, SJ ;
LEDER, P .
CELL, 1995, 82 (04) :675-684
[22]   Cellular and subcellular localization of six retinoid receptors in rat testis during postnatal development: Identification of potential heterodimeric receptors [J].
Dufour, JM ;
Kim, KH .
BIOLOGY OF REPRODUCTION, 1999, 61 (05) :1300-1308
[23]   PITUITARY-GONADAL AXIS BEFORE PUBERTY - EVALUATION OF TESTICULAR STEROIDS IN MALE RAT [J].
ELDRIDGE, JC ;
MAHESH, VB .
BIOLOGY OF REPRODUCTION, 1974, 11 (04) :385-397
[24]   A syndrome of multiorgan hyperplasia with features of gigantism, tumorigenesis, and female sterility in p27(Kip1)-deficient mice [J].
Fero, ML ;
Rivkin, M ;
Tasch, M ;
Porter, P ;
Carow, CE ;
Firpo, E ;
Polyak, K ;
Tsai, LH ;
Broudy, V ;
Perlmutter, RM ;
Kaushansky, K ;
Roberts, JM .
CELL, 1996, 85 (05) :733-744
[25]   EFFECT OF THYROID-HORMONE ON THE PRENATAL AND POSTNATAL-DEVELOPMENT OF THE RAT TESTIS [J].
FRANCAVILLA, S ;
CORDESCHI, G ;
PROPERZI, G ;
DICICCO, L ;
JANNINI, EA ;
PALMERO, S ;
FUGASSA, E ;
LORAS, B ;
DARMIENTO, M .
JOURNAL OF ENDOCRINOLOGY, 1991, 129 (01) :35-+
[26]  
Fuqua JS, 1996, HUM GENET, V97, P506
[27]   RETINOIDS REGULATE GONADOTROPIN ACTION IN CULTURED RAT SERTOLI CELLS [J].
GALDIERI, M ;
NISTICO, L .
BIOLOGY OF REPRODUCTION, 1994, 50 (01) :171-177
[28]   Preserved male fertility despite decreased androgen sensitivity caused by a mutation in the ligand-binding domain of the androgen receptor gene [J].
Giwercman, A ;
Kledal, T ;
Schwartz, M ;
Giwercman, YL ;
Leffers, H ;
Zazzi, H ;
Wedell, A ;
Skakkebæk, NE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2000, 85 (06) :2253-2259
[29]   ADULT TESTICULAR ENLARGEMENT INDUCED BY NEONATAL-HYPOTHYROIDISM IS ACCOMPANIED BY INCREASED SERTOLI AND GERM-CELL NUMBERS [J].
HESS, RA ;
COOKE, PS ;
BUNICK, D ;
KIRBY, JD .
ENDOCRINOLOGY, 1993, 132 (06) :2607-2613
[30]   Thyroid hormone regulates the cell cycle inhibitor p27Kip1 in postnatal murine Sertoli cells [J].
Holsberger, DR ;
Jirawatnotai, S ;
Kiyokawa, H ;
Cooke, PS .
ENDOCRINOLOGY, 2003, 144 (09) :3732-3738