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培养的牛垂体细胞中生长激素分泌和信使核糖核酸积累的激素调节

Hormonal regulation of growth hormone secretion and messenger ribonucleic acid accumulation in cultured bovine pituitary cells.

作者信息

Silverman B L, Kaplan S L, Grumbach M M, Miller W L

机构信息

Department of Pediatrics, University of California, San Francisco 94143.

出版信息

Endocrinology. 1988 Apr;122(4):1236-41. doi: 10.1210/endo-122-4-1236.

Abstract

In both primary cultures and transformed tumor cultures of rat pituitary cells, preincubation with T3 or dexamethasone increases GH secretion, mRNA accumulation, and gene transcription. GRF stimulates secretion and transcription in primary rat pituitary cultures. Sex steroids stimulate GH secretion in man, but contradictory findings have been reported in vitro. We studied the hormonal regulation of bovine GH (bGH) in primary monolayer cultures of adult bovine pituitaries. Neither T3 nor dexamethasone changed immunoreactive bGH secretion during a 3-h experimental incubation. After 72-h preincubation with T3 or dexamethasone, bGH secretion remained unchanged. T3 (10(-8) M) or dexamethasone (10(-8) M) did not alter the bGH secretory response to doses of GRF from 10(-12)-10(-8) M. However, T3 (P less than 0.001; r = 0.73) and dexamethasone (P less than 0.001; r = -0.71) decreased bGH mRNA content in dose-dependent fashions, as determined by Northern analysis and RNA dot blots probed with 32P-labeled bGH cDNA. T3 10(-7) M) decreased bGH mRNA content to 70% of the control value, 10(-7) M dexamethasone decreased bGH mRNA content to 77% of the control value, while GRF increased bGH mRNA content to 174% of the control value in a dose-dependent fashion (P less than 0.001; r = 0.72). Preincubation with testosterone or dihydrotestosterone did not change basal or GRF-stimulated GH secretion. Seventy-two-hour preincubation with 10(-8) M estradiol did not alter basal GH secretion, but increased the bGH secretory response to doses of GRF from 10(-11)-10(-8) M (P less than 0.001). Incubation with estradiol did not change bGH mRNA levels. These results demonstrate that, in contrast to rat GH mRNA, bGH mRNA accumulation is inhibited by T3 and dexamethasone. Estradiol augments the response to GRF, but this effect is not mediated by an increase in mRNA content. The hormonal responses of somatotropes vary significantly among mammalian species.

摘要

在大鼠垂体细胞的原代培养物和转化的肿瘤培养物中,用三碘甲状腺原氨酸(T3)或地塞米松预孵育可增加生长激素(GH)分泌、mRNA积累和基因转录。生长激素释放因子(GRF)可刺激原代大鼠垂体培养物中的分泌和转录。性类固醇可刺激人类的GH分泌,但体外研究结果相互矛盾。我们研究了成年牛垂体原代单层培养物中牛GH(bGH)的激素调节。在3小时的实验孵育期间,T3和地塞米松均未改变免疫反应性bGH的分泌。用T3或地塞米松预孵育72小时后,bGH分泌保持不变。T3(10^(-8) M)或地塞米松(10^(-8) M)并未改变bGH对10^(-12) - 10^(-8) M剂量GRF的分泌反应。然而,通过Northern分析和用32P标记的bGH cDNA探针进行的RNA斑点印迹法测定,T3(P < 0.001;r = 0.73)和地塞米松(P < 0.001;r = -0.71)以剂量依赖方式降低了bGH mRNA含量。10^(-7) M的T3将bGH mRNA含量降低至对照值的70%,10^(-7) M的地塞米松将bGH mRNA含量降低至对照值的77%,而GRF以剂量依赖方式将bGH mRNA含量增加至对照值的174%(P < 0.001;r = 0.72)。用睾酮或二氢睾酮预孵育未改变基础或GRF刺激的GH分泌。用10^(-8) M雌二醇预孵育72小时未改变基础GH分泌,但增加了bGH对10^(-11) - 10^(-8) M剂量GRF的分泌反应(P < 0.001)。用雌二醇孵育未改变bGH mRNA水平。这些结果表明,与大鼠GH mRNA不同,bGH mRNA积累受到T3和地塞米松的抑制。雌二醇增强了对GRF的反应,但这种作用不是由mRNA含量增加介导的。不同哺乳动物物种中生长激素细胞的激素反应差异显著。

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