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培养的大鼠腹侧前列腺中前列腺蛋白合成与分泌的多激素调控

Multihormonal control of synthesis and secretion of prostatein in cultured rat ventral prostate.

作者信息

Martikainen P, Härkönen P, Vanhala T, Mäkelä S, Viljanen M, Suominen J

出版信息

Endocrinology. 1987 Aug;121(2):604-11. doi: 10.1210/endo-121-2-604.

DOI:10.1210/endo-121-2-604
PMID:3297650
Abstract

The synthesis and accumulation of prostatein, a major secretory protein of the rat ventral prostate, was examined in organ culture conditions. For the quantitation of this protein in the medium, a sensitive enzyme immunoassay was developed. The rat ventral prostate could be maintained in organ culture in defined medium for at least 2 weeks. Morphologically the changes in explants cultured without hormones resembled those of castration. These involutive changes could be postponed by testosterone and totally prevented by a combination of testosterone, corticosterone, and insulin in the culture medium. Newly synthesized prostatein, studied by fluorography of [35S] methionine-labeled proteins, accumulated only in the presence of testosterone. Its synthesis also took place in cultured prostate derived from castrated rats. Neither corticosterone nor insulin alone could sustain prostatein synthesis. Insulin increased the testosterone-dependent prostatein synthesis in the beginning of culture, but later, inhibition, rather than stimulation, could be noted. Corticosterone increased the testosterone-dependent synthesis of prostatein throughout the culture. The results show that organ culture of adult rat ventral prostate provides an in vitro model for studies of differentiated prostatic function.

摘要

在器官培养条件下,对大鼠腹侧前列腺的主要分泌蛋白前列腺蛋白的合成与积累进行了研究。为了定量培养基中的这种蛋白质,开发了一种灵敏的酶免疫测定法。大鼠腹侧前列腺可以在限定培养基中进行器官培养至少2周。在形态学上,无激素培养的外植体的变化类似于去势后的变化。这些退化性变化可被睾酮推迟,并且在培养基中加入睾酮、皮质酮和胰岛素的组合可完全防止。通过对[35S]甲硫氨酸标记的蛋白质进行放射自显影研究发现,新合成的前列腺蛋白仅在有睾酮存在时积累。其合成也发生在去势大鼠的培养前列腺中。单独的皮质酮或胰岛素都不能维持前列腺蛋白的合成。胰岛素在培养开始时增加了睾酮依赖性前列腺蛋白的合成,但后来,观察到的是抑制而非刺激作用。在整个培养过程中,皮质酮增加了睾酮依赖性前列腺蛋白的合成。结果表明,成年大鼠腹侧前列腺的器官培养为研究分化的前列腺功能提供了一个体外模型。

相似文献

1
Multihormonal control of synthesis and secretion of prostatein in cultured rat ventral prostate.培养的大鼠腹侧前列腺中前列腺蛋白合成与分泌的多激素调控
Endocrinology. 1987 Aug;121(2):604-11. doi: 10.1210/endo-121-2-604.
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Interaction of male and female sex hormones in cultured rat prostate.雄性和雌性性激素在培养的大鼠前列腺中的相互作用。
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Prostatein C3-mRNA: a sensitive marker of androgen-responsiveness in prostate explant cultures.前列腺素C3信使核糖核酸:前列腺外植体培养中雄激素反应性的敏感标志物。
Prostate. 1990;17(1):41-55. doi: 10.1002/pros.2990170106.
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4-MAPC, a 5 alpha-reductase inhibitor, reduces rat ventral prostate weight, DNA, and prostatein concentrations.4-MAPC,一种5α-还原酶抑制剂,可降低大鼠腹侧前列腺重量、DNA及前列腺素浓度。
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Regulation of gene expression in rat prostate by androgen and beta-adrenergic receptor pathways.雄激素和β-肾上腺素能受体途径对大鼠前列腺基因表达的调控。
Mol Endocrinol. 1990 Sep;4(9):1343-53. doi: 10.1210/mend-4-9-1343.
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Influence of castration and androgen treatment on the synthesis of prostatic binding protein and the concentration of its mRNA in the rat ventral prostate.去势和雄激素治疗对大鼠前列腺腹叶中前列腺结合蛋白合成及其mRNA浓度的影响。
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Stimulation of androgen-dependent gene expression by the adrenal precursors dehydroepiandrosterone and androstenedione in the rat ventral prostate.肾上腺前体脱氢表雄酮和雄烯二酮对大鼠腹侧前列腺雄激素依赖性基因表达的刺激作用。
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Developmental aspects of androgen-dependent mRNA from rat ventral prostate using cloned cDNA.
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Expression of androgen receptors and prostatic steroid-binding protein during development of the rat ventral prostate.大鼠腹侧前列腺发育过程中雄激素受体和前列腺类固醇结合蛋白的表达
J Endocrinol. 1988 Jun;117(3):361-6. doi: 10.1677/joe.0.1170361.

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Estrogen and estrogen receptor alpha promotes malignancy and osteoblastic tumorigenesis in prostate cancer.雌激素和雌激素受体α促进前列腺癌的恶性肿瘤形成和成骨细胞肿瘤发生。
Oncotarget. 2015 Dec 29;6(42):44388-402. doi: 10.18632/oncotarget.6317.
2
Prolactin and prolactin receptors are expressed and functioning in human prostate.催乳素及催乳素受体在人类前列腺中表达并发挥作用。
J Clin Invest. 1997 Feb 15;99(4):618-27. doi: 10.1172/JCI119204.
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Post-natal development modulates the rat seminal vesicle sensitivity to sympathomimetic agonists.
产后发育调节大鼠精囊对拟交感神经激动剂的敏感性。
Naunyn Schmiedebergs Arch Pharmacol. 1993 Jul;348(1):53-7. doi: 10.1007/BF00168536.