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重组人促甲状腺激素对人促甲状腺激素(TSH)受体信使核糖核酸的正向调节作用发生在细胞核内水平。

The positive regulation of human thyrotropin (TSH) receptor messenger ribonucleic acid by recombinant human TSH is at the intranuclear level.

作者信息

Huber G K, Weinstein S P, Graves P N, Davies T F

机构信息

Department of Medicine, Mount Sinai School of Medicine, New York, New York 10029.

出版信息

Endocrinology. 1992 May;130(5):2858-64. doi: 10.1210/endo.130.5.1572298.

Abstract

We have assessed the regulatory influence of human recombinant TSH (rec-hTSH) on its homologous receptor (TSHR) using a well characterized human fetal thyroid monolayer cell culture technique. Under the culture conditions employed, fetal human thyroid cells showed basal expression of TSHR-specific mRNA transcripts, and the addition of rec-hTSH (1 U/L) induced up to an 8-fold increase in specific mRNA over a 48-h observation period. This induction was simulated by bromo-cAMP in a dose-dependent manner, indicating that the stimulatory effect of rec-hTSH was active at the postreceptor level. Furthermore, there was no detectable increase in the transcription rate of the TSHR gene after stimulation with rec-hTSH for 12-36 h, although a marked increase in thyroglobulin-specific mRNA was observed. Rec-hTSH also had no influence on the half-life of TSHR-specific mRNA, which remained at approximately 16 h in the presence or absence of rec-hTSH. These data indicate that rec-hTSH induced up-regulation in human thyroid cell TSHR-specific mRNA and that the mechanism of this regulation was likely to be secondary to a posttranscriptional nuclear event involving changes in the regulation of primary unspliced mRNA for the TSHR.

摘要

我们采用一种特性明确的人胎儿甲状腺单层细胞培养技术,评估了重组人促甲状腺激素(rec-hTSH)对其同源受体(TSHR)的调节作用。在所采用的培养条件下,人胎儿甲状腺细胞呈现TSHR特异性mRNA转录本的基础表达,在48小时的观察期内,添加rec-hTSH(1 U/L)可使特异性mRNA增加多达8倍。这种诱导作用可被溴化环磷腺苷以剂量依赖的方式模拟,表明rec-hTSH的刺激作用在受体后水平发挥作用。此外,用rec-hTSH刺激12 - 36小时后,TSHR基因的转录速率未检测到增加,尽管观察到甲状腺球蛋白特异性mRNA有显著增加。Rec-hTSH对TSHR特异性mRNA的半衰期也没有影响,无论有无rec-hTSH,其半衰期均保持在约16小时。这些数据表明,rec-hTSH可诱导人甲状腺细胞TSHR特异性mRNA上调,且这种调节机制可能继发于转录后核事件,涉及TSHR初级未剪接mRNA调控的变化。

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