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甲状腺激素受体β缺陷小鼠中甲状腺激素对促甲状腺激素的调节

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

作者信息

Weiss R E, Forrest D, Pohlenz J, Cua K, Curran T, Refetoff S

机构信息

Department of Medicine, The University of Chicago, Illinois 60637, USA.

出版信息

Endocrinology. 1997 Sep;138(9):3624-9. doi: 10.1210/endo.138.9.5412.

DOI:10.1210/endo.138.9.5412
PMID:9275045
Abstract

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 beta1 and TR beta2 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-T3 and L-T4. 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-T3 and L-T4 was severely blunted in TR beta-/- mice, and full suppression was not achieved with the maximal L-T3 dose of 25 microg/day x 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.

摘要

甲状腺激素反应性基因可受到甲状腺激素的正向和负向调节。促甲状腺激素(TSH)受甲状腺激素下调,在甲状腺激素缺乏时升高。由于甲状腺激素受体(TR)α和β基因均在垂体中表达,因此尚不清楚TRα和TRβ在TSH调节中的相对作用。使用人工基因过表达的实验得出了相互矛盾的结果。缺乏TRβ1和TRβ2两种亚型的TRβ基因敲除小鼠提供了一个模型,用于研究这些受体在TSH调节中的作用。通过给同一品系的TRβ缺陷(TRβ-/-)和野生型(TRβ+/+)小鼠喂食含丙硫氧嘧啶的低碘饮食使其甲状腺激素缺乏,然后用不同剂量的L-T3和L-T4进行治疗。甲状腺激素缺乏迅速增加了TRβ+/+和TRβ-/-小鼠的血清TSH水平,在无甲状腺激素时达到相似水平。相反,TRβ-/-小鼠中用L-T3和L-T4治疗导致的血清TSH下降严重减弱,给予最大剂量25μg/天·只小鼠的L-T3也未实现完全抑制。这些数据表明,在甲状腺激素缺乏时TSH上调不需要TRβ。然而,虽然单独的TRα可以介导甲状腺激素诱导的TSH抑制,但TRβ增强了TSH下调的敏感性,可能对TSH的完全抑制至关重要。

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