Transcriptional regulation of iodothyronine deiodinases during embryonic development

被引:55
作者
Van der Geyten, S
Segers, I
Gereben, B
Bartha, T
Rudas, P
Larsen, PR
Kühn, ER
Darras, VM
机构
[1] Katholieke Univ Leuven, Inst Zool, Lab Comparat Endocrinol, B-3000 Louvain, Belgium
[2] Szent Istvan Univ, Fac Vet Sci, Dept Physiol & Biochem, H-1400 Budapest, Hungary
[3] Brigham & Womens Hosp, Dept Med, Div Thyroid, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
关键词
thyroid hormone; deiodination; dexamethasone; growth hormone; chicken;
D O I
10.1016/S0303-7207(01)00644-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A single dose of chicken growth hormone (cGH) or dexamethasone acutely increases circulating T-3 levels in 18-day-old chicken embryos through a reduction of hepatic type III iodothyronine deiodinase (D3). The data in the present study suggest that this decrease in D3 is induced by a direct downregulation of hepatic D3 gene transcription, The lack of effect of cGH or dexamethasone on brain and kidney D3 activity, furthermore suggests that both hormones affect peripheral thyroid hormone metabolism in a tissue specific manner, Dexamethasone administration also results in an increase in brain type II iodothyronine deiodinase (D2) activity and mRNA levels that is also regulated at a transcriptional level. In contrast, however, cGH has no effect on brain D2 activity, thereby suggesting that either GH cannot pass through the blood-brain barrier in chicken or that cGH and dexamethasone regulate thyroid hormone deiodination by different mechanisms. In addition, the very short half-life of D2 and D3 (t(1 2) < 1 h) in comparison with the longer half life of type I iodothyronine deiodinase (D1, t(1 2) > 8 h), allows for D2 and D3 to play a more prominent role in the acute regulation of peripheral thyroid hormone metabolism than D1. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
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页码:1 / 9
页数:9
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