Thyrotropin regulation by thyroid hormone in thyroid hormone receptor beta-deficient mice

被引:80
作者
Weiss, RE
Forrest, D
Pohlenz, J
Cua, K
Curran, T
Refetoff, S
机构
[1] UNIV CHICAGO, DEPT PEDIAT, CHICAGO, IL 60637 USA
[2] UNIV CHICAGO, JP KENNEDY JR MENTAL RETARDAT RES CTR, CHICAGO, IL 60637 USA
[3] MT SINAI MED CTR, DEPT HUMAN GENET, NEW YORK, NY 10029 USA
[4] ST JUDE CHILDRENS RES HOSP, DEPT DEV NEUROBIOL, MEMPHIS, TN 38105 USA
关键词
D O I
10.1210/en.138.9.3624
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Thyroid hormone responsive genes can be both positively and negatively regulated by thyroid hormone. TSH is down-regulated by thyroid hormone and rises during thyroid hormone deprivation. Because both thyroid hormone receptor (TR) alpha and beta genes are expressed in the pituitary gland, it is unclear what the relative roles of TR alpha and TR beta are in TSH regulation. Experiments using over expression of artificial genes have yielded conflicting results. The TR beta knock-out mouse that lacks both TR beta 1 and TR beta 2 isoforms provides a model to examine the role of these receptors in TSH regulation. TR beta deficient (TR beta-/-) and wild-type (TR beta+/+) mice of the same strain were deprived of thyroid hormone by feeding them a low iodine diet containing propylthiouracil and were then treated with different doses of L-T-3 and L-T-4. Thyroid hormone deprivation rapidly increased the serum TSH level in both TR beta+/+ and TR beta-/- mice, reaching a similar level in the absence of thyroid hormone. In contrast, the decline of serum TSH by treatment with both L-T-3 and L-T-4 was severely blunted in TR beta-/- mice, and full suppression was not achieved with the maximal L-T-3 dose of 25 mu g/day.mouse. These data indicate that TR beta is not required for the up-regulation of TSH in thyroid hormone deficiency. However, although TR alpha alone can mediate thyroid hormone induced TSH suppression, TR beta enhances the sensitivity of TSH down-regulation and may be essential for the complete suppression of TSH.
引用
收藏
页码:3624 / 3629
页数:6
相关论文
共 26 条
[21]   FAMILIAL SYNDROME COMBINING DEAF-MUTISM STIPPLED EPIPHYSES GOITER AND ABNORMALLY HIGH PBI - POSSIBLE TARGET ORGAN REFRACTORINESS TO THYROID HORMONE [J].
REFETOFF, S ;
DEWIND, LT ;
DEGROOT, LJ .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1967, 27 (02) :279-+
[22]  
SANDHOFER C, 1996, THYROID S1, V1, pS32
[23]  
SCHWARTZ HL, 1994, J BIOL CHEM, V269, P24777
[24]   RECESSIVE INHERITANCE OF THYROID-HORMONE RESISTANCE CAUSED BY COMPLETE DELETION OF THE PROTEIN-CODING REGION OF THE THYROID-HORMONE RECEPTOR-BETA GENE [J].
TAKEDA, K ;
SAKURAI, A ;
DEGROOT, LJ ;
REFETOFF, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1992, 74 (01) :49-55
[25]   STUDIES ON THE REPRESSION OF BASAL TRANSCRIPTION (SILENCING) BY ARTIFICIAL AND NATURAL HUMAN THYROID-HORMONE RECEPTOR-BETA MUTANTS [J].
YEN, PM ;
WILCOX, EC ;
HAYASHI, Y ;
REFETOFF, S ;
CHIN, WW .
ENDOCRINOLOGY, 1995, 136 (07) :2845-2851
[26]  
ZHANG XK, 1991, NEW BIOL, V3, P169