Suppr超能文献

促甲状腺激素可刺激人成骨细胞中2型碘甲状腺原氨酸脱碘酶的表达。

Expression of type 2 iodothyronine deiodinase in human osteoblast is stimulated by thyrotropin.

作者信息

Morimura Tadashi, Tsunekawa Katsuhiko, Kasahara Takayuki, Seki Koji, Ogiwara Takayuki, Mori Masatomo, Murakami Masami

机构信息

Department of Clinical Laboratory Medicine, Gunma University Graduate School of Medicine, Maebashi 371-8511, Japan.

出版信息

Endocrinology. 2005 Apr;146(4):2077-84. doi: 10.1210/en.2004-1432. Epub 2005 Jan 13.

Abstract

Thyroid hormones play important roles in bone growth, development, and turnover. To exert its biological activity, T(4) needs to be converted to T(3) by iodothyronine deiodinase. In human thyroid gland as well as rat brown adipose tissue, type 2 iodothyronine deiodinase (D2) expression is regulated by a TSH receptor-cAMP-mediated mechanism. TSH receptor knockout mice demonstrated the direct effects of TSH on bone via TSH receptors found on osteoblast and osteoclast precursors. In the present study we investigated the possible expression and function of iodothyronine deiodinase and TSH receptors in human osteoblast-like osteosarcoma (SaOS-2) cells and normal human osteoblast (NHOst) cells. Iodothyronine deiodinase activity was detected in SaOS-2 cells and NHOst cells, and all of the characteristics of deiodinating activity were compatible with those of D2. Northern analysis demonstrated D2 mRNA expression in SaOS-2 cells and NHOst cells. D2 mRNA levels as well as D2 activities were rapidly increased by dibutyryl cAMP or forskolin in SaOS-2 cells and NHOst cells. TSH receptor mRNA was demonstrated in SaOS-2 cells and NHOst cells, and D2 mRNA and D2 activity were stimulated by TSH in both cells. In addition, all T(3) receptor isoforms were detected by RT-PCR in SaOS-2 cells and NHOst cells. The present results indicate the expression of functional TSH receptors and D2 in human osteoblasts and suggest previously unrecognized roles of TSH receptors and local T(3) production by D2 in the pathophysiology of human osteoblasts.

摘要

甲状腺激素在骨骼生长、发育和代谢中发挥着重要作用。为发挥其生物学活性,T4需要通过碘甲状腺原氨酸脱碘酶转化为T3。在人类甲状腺以及大鼠棕色脂肪组织中,2型碘甲状腺原氨酸脱碘酶(D2)的表达受促甲状腺激素受体 - cAMP介导机制的调节。促甲状腺激素受体基因敲除小鼠证明了促甲状腺激素通过成骨细胞和破骨细胞前体上发现的促甲状腺激素受体对骨骼产生直接影响。在本研究中,我们调查了碘甲状腺原氨酸脱碘酶和促甲状腺激素受体在人成骨样骨肉瘤(SaOS - 2)细胞和正常人成骨细胞(NHOst)细胞中的可能表达及功能。在SaOS - 2细胞和NHOst细胞中检测到了碘甲状腺原氨酸脱碘酶活性,并且脱碘活性的所有特征都与D2相符。Northern分析证明了SaOS - 2细胞和NHOst细胞中有D2 mRNA表达。在SaOS - 2细胞和NHOst细胞中,二丁酰cAMP或福斯可林可使D2 mRNA水平以及D2活性迅速增加。在SaOS - 2细胞和NHOst细胞中证明了促甲状腺激素受体mRNA的存在,并且在这两种细胞中促甲状腺激素均可刺激D2 mRNA和D2活性。此外,通过RT - PCR在SaOS - 2细胞和NHOst细胞中检测到了所有T3受体亚型。目前的结果表明功能性促甲状腺激素受体和D2在人成骨细胞中的表达,并提示促甲状腺激素受体和D2产生的局部T3在人成骨细胞病理生理学中具有先前未被认识到的作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验