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生长激素基因转录在体内和体外的周期性调控。

Cyclic regulation of growth hormone gene transcription in vivo and in vitro.

作者信息

Nyborg J K, Nguyen A P, Spindler S R

出版信息

Endocrinology. 1985 Jun;116(6):2361-5. doi: 10.1210/endo-116-6-2361.

Abstract

The in vivo thyroid and glucocorticoid hormone regulation of GH gene transcription was compared with that found in cultured GH rat pituitary tumor cells. The GH cell lines have been widely used to study GH gene expression, but their relevance to the in vivo regulation of the gene has not been well established. The in vivo studies described here utilized rats that were both thyroparathyroidectomized and adrenalectomized to remove the organ sources of these hormones. The in vitro studies described utilized GC cells hormonally deinduced in medium lacking the hormones. Continuous administration of glucocorticoid or thyroid hormones to either system induced multiple cycles of GH transcriptional activation and deactivation. These cycles were accompanied by cycles of increasing and decreasing GH messenger RNA. In both systems, a brief transcription cycle occurred within hours of thyroid or glucocorticoid hormone addition, and a second broad occurred between 3 and 11 days later. These cycles were independent of changes in receptor levels. The similarities in the responses found in vivo and in cell culture suggest that the molecular mechanisms regulating expression of the GH gene appropriately function in GC cells, despite their transformed phenotype and prolonged maintenance in culture. Thus, these cell lines appear to be appropriate model systems for studies of thyroid and glucocorticoid hormone action.

摘要

将生长激素(GH)基因转录的体内甲状腺激素和糖皮质激素调节与培养的大鼠垂体肿瘤GH细胞中的调节情况进行了比较。GH细胞系已被广泛用于研究GH基因表达,但其与该基因体内调节的相关性尚未得到充分证实。此处描述的体内研究使用了甲状腺甲状旁腺切除和肾上腺切除的大鼠,以去除这些激素的器官来源。所描述的体外研究使用了在缺乏激素的培养基中进行激素去诱导的GC细胞。向任一系统持续施用糖皮质激素或甲状腺激素会诱导GH转录激活和失活的多个循环。这些循环伴随着GH信使核糖核酸的增减循环。在两个系统中,在添加甲状腺或糖皮质激素后的数小时内会出现一个短暂的转录循环,第二个广泛的循环在3至11天后出现。这些循环与受体水平的变化无关。在体内和细胞培养中发现的反应相似性表明,尽管GC细胞具有转化表型且在培养中维持时间较长,但调节GH基因表达的分子机制在GC细胞中仍能正常发挥作用。因此,这些细胞系似乎是研究甲状腺和糖皮质激素作用的合适模型系统。

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