Li M, Boyages S C
Department of Diabetes and Endocrinology, Westmead Hospital, NSW, Australia.
Brain Res. 1997 Oct 31;773(1-2):125-31. doi: 10.1016/s0006-8993(97)00917-7.
Recently, we have shown an extended distribution pattern of the TR-beta2 isoform in specific sites of rat brain which may be indicative that the localization of this receptor also confers functional specificity. The beta2 thyroid hormone receptor (TR-beta2) is by far the most abundant isoform in the pituitary, although transcripts of TR-alpha and TR-beta1 genes have been reported in developmental and adult rat pituitary gland. Using both in situ hybridization histochemistry (ISH) and immunocytochemistry, we mapped the expression of beta2 thyroid hormone receptor mRNA and protein in euthyroid and hypothyroid adult rat pituitary, particularly in relation to the thyrotrope population. TR-beta2 mRNA localization by ISH showed an anteromedial spatial distribution pattern in euthyroid rat anterior pituitary gland. This localization coincided with the immunostaining pattern for thyrotropes. TR-beta2-immunoreactive cells showed strongly positive signals in the nuclei. Hypothyroidism, induced by propylthiouracil (PTU), abolished the specific localization of TR-beta2 mRNA and upregulated the transcription of TR-beta2 mRNA in vivo and in vitro. Image analysis revealed that the optical density signals within hypothyroid rat pituitary were significantly stronger (2.6-fold) compared with euthyroid counterparts. This correlated strongly with an increased number and staining of TR-beta2 protein positive cells, demonstrating both nuclear and cytoplasmic staining. In response to thyroid hormone deficiency, there was also a marked percentage increase in the thyrotrope population from 10 to 20% of anterior pituitary cells to approximately 80%. In conclusion, these results demonstrate the specific localization of TR-beta2 to the anterior pituitary, especially to the thyrotrope population, and its regulation by thyroid hormone. Hypothyroidism leads to an upregulation of TR-beta2 mRNA and protein in the anterior pituitary, explained not only by an absolute increase in the percentage of thyrotropes but increased expression of TR-beta2 mRNA and protein per cell. These data allude to the TR-beta2 isoform playing a critical role in thyroid hormone-dependent TSH gene expression, although contributions from the other TR isoforms may still remain important.
最近,我们已经证明大鼠脑特定部位存在TR-β2亚型的扩展分布模式,这可能表明该受体的定位也赋予了功能特异性。β2甲状腺激素受体(TR-β2)是垂体中迄今为止最丰富的亚型,尽管在发育中的和成年大鼠垂体中已报道了TR-α和TR-β1基因的转录本。我们使用原位杂交组织化学(ISH)和免疫细胞化学方法,绘制了正常甲状腺和甲状腺功能减退成年大鼠垂体中β2甲状腺激素受体mRNA和蛋白的表达图谱,特别是与促甲状腺激素细胞群体的关系。ISH显示TR-β2 mRNA在正常甲状腺大鼠垂体前叶呈前内侧空间分布模式。这种定位与促甲状腺激素细胞的免疫染色模式一致。TR-β2免疫反应性细胞在细胞核中显示出强阳性信号。丙硫氧嘧啶(PTU)诱导的甲状腺功能减退消除了TR-β2 mRNA的特异性定位,并在体内和体外上调了TR-β2 mRNA的转录。图像分析显示,甲状腺功能减退大鼠垂体中的光密度信号与正常甲状腺大鼠相比显著更强(2.6倍)。这与TR-β2蛋白阳性细胞数量和染色增加密切相关,显示出细胞核和细胞质染色。对甲状腺激素缺乏的反应中,促甲状腺激素细胞群体也有显著的百分比增加,从前叶垂体细胞的10%至20%增加到约80%。总之,这些结果证明了TR-β2在前叶垂体,特别是促甲状腺激素细胞群体中的特异性定位及其受甲状腺激素的调节。甲状腺功能减退导致前叶垂体中TR-β2 mRNA和蛋白上调,这不仅是由于促甲状腺激素细胞百分比的绝对增加,还由于每个细胞中TR-β2 mRNA和蛋白表达的增加。这些数据表明TR-β2亚型在甲状腺激素依赖性促甲状腺激素基因表达中起关键作用,尽管其他TR亚型的贡献可能仍然很重要。