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重组人激活素A对人生长激素瘤体外生长激素分泌的影响。

Effects of recombinant human activin A on growth hormone secretion by human somatotrophinomas in vitro.

作者信息

Daniels M, Harris P E, James R A, Turner S J, Dewar J H, Kendall-Taylor P

机构信息

Department of Medicine, Medical School, Newcastle upon Tyne, U.K.

出版信息

J Endocrinol. 1993 May;137(2):329-34. doi: 10.1677/joe.0.1370329.

Abstract

Activin A is a homodimer of inhibin beta A subunits, and was first isolated from gonadal fluids on the basis of its ability to stimulate FSH secretion by rat pituitary cells in vitro. The beta A subunits of activin and their mRNAs have been found in many cell types, in several species and at different stages of development, suggesting that activin A has a wide range of diverse biological roles. Apart from the modulation of gonadotroph function, in-vitro studies have demonstrated inhibitory effects of activin A on GH synthesis, GH secretion and possibly somatotroph proliferation. We have therefore investigated the potential role of activin A in the pathophysiological regulation of GH secretion by human somatotrophinoma cells using in-vitro techniques. Cell cultures were established by enzyme dispersion of adenoma tissue obtained from six patients with acromegaly, and treated for 72 h with 0.01-10 nmol recombinant human activin A/l followed by a 2-h stimulation test with 10 nmol GH-releasing factor (GRF)/l. Medium was collected at 24, 48 and 72 h, as well as after GRF treatment, and GH concentrations were measured by immunoradiometric assay. Basal GH secretion from the cells of two tumours was significantly stimulated 12-63% above control values during treatment with 0.01-10 nmol activin A/l, whereas the peptide had no effect on GH release from cells of the remainder of the tumours. GRF significantly stimulated GH release from the cells of two different adenomas, and pretreatment with 0.01-1 nmol activin A/1 partially but significantly blocked GRF-stimulated GH release from the cells of one of these.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

激活素A是抑制素βA亚基的同型二聚体,最初是从性腺液中分离出来的,其依据是它在体外能够刺激大鼠垂体细胞分泌促卵泡激素。在多个物种的许多细胞类型以及不同发育阶段都发现了激活素的βA亚基及其信使核糖核酸,这表明激活素A具有广泛多样的生物学作用。除了调节促性腺激素细胞功能外,体外研究还表明激活素A对生长激素的合成、分泌以及可能对生长激素细胞的增殖具有抑制作用。因此,我们利用体外技术研究了激活素A在人生长激素瘤细胞分泌生长激素的病理生理调节中的潜在作用。通过酶分散从6例肢端肥大症患者获得的腺瘤组织建立细胞培养物,并用0.01 - 10纳摩尔重组人激活素A/升处理72小时,随后用10纳摩尔生长激素释放因子(GRF)/升进行2小时刺激试验。在24、48和72小时以及GRF处理后收集培养基,通过免疫放射测定法测量生长激素浓度。在用0.01 - 10纳摩尔激活素A/升处理期间,两个肿瘤细胞的基础生长激素分泌比对照值显著增加了12 - 63%,而该肽对其余肿瘤细胞的生长激素释放没有影响。GRF显著刺激了两个不同腺瘤细胞的生长激素释放,并且用0.01 - 1纳摩尔激活素A/升预处理部分但显著地阻断了其中一个腺瘤细胞对GRF刺激的生长激素释放。(摘要截短至250字)

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