首页> 外文期刊>Molecular and Cellular Endocrinology >Insulin regulation of growth hormone receptor gene expression Evidence for a transcriptional mechanism of down-regulation in rat hepatoma cells.
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Insulin regulation of growth hormone receptor gene expression Evidence for a transcriptional mechanism of down-regulation in rat hepatoma cells.

机译:胰岛素调节生长激素受体基因表达的证据是大鼠肝癌细胞中下调的转录机制的证据。

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摘要

The role of insulin in regulating responsiveness to growth hormone (GH) remains unclear. Continuous insulin treatment reduces GH binding, which suggests that insulin may effect growth hormone receptor (GHR) levels. The present study used rat hepatoma cells to examine the effects of insulin and GH on GHR gene expression. Prolonged insulin treatment (greater than 3h) significantly reduced GHR mRNA, and removal of insulin led to a gradual recovery. This effect of insulin occurred at physiologic concentrations, occurred many hours before the insulin-regulated decrease in GHR protein, and was mediated by reduction of GHR transcription. GH treatment dramatically reduced GHR protein, but caused only a modest reduction in GHR mRNA. These findings indicate that the heterologous reduction of GHR by insulin occurs via transcriptional downregulation, and the homologous reduction of GHR by GH occurs via a different mechanism. Furthermore, with insulin, extended time of exposure may be necessary for appreciable reduction of GHR.
机译:胰岛素在调节对生长激素(GH)的反应性中的作用尚不清楚。持续的胰岛素治疗减少了GH的结合,这表明胰岛素可能会影响生长激素受体(GHR)的水平。本研究使用大鼠肝癌细胞来检查胰岛素和生长激素对GHR基因表达的影响。长时间的胰岛素治疗(大于3小时)会显着降低GHR mRNA,并且去除胰岛素会导致逐渐恢复。胰岛素的这种作用发生在生理浓度下,发生在胰岛素调节的GHR蛋白下降之前的许多小时,并由GHR转录的降低介导。 GH治疗可显着降低GHR蛋白,但仅引起GHR mRNA适度降低。这些发现表明,胰岛素的GHR异源降低是通过转录下调发生的,而GH的GHR同源降低是通过不同的机制发生的。此外,对于胰岛素,可能需要延长暴露时间以显着降低GHR。

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