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孕酮和人绒毛膜促性腺激素在体外不刺激人蜕膜组织产生胎盘蛋白12和14或催乳素。

Progesterone and human chorionic gonadotropin do not stimulate placental proteins 12 and 14 or prolactin production by human decidual tissue in vitro.

作者信息

Ren S G, Braunstein G D

机构信息

Department of Medicine, Cedars-Sinai Medical Center, University of California School of Medicine, Los Angeles 90048.

出版信息

J Clin Endocrinol Metab. 1990 Apr;70(4):983-9. doi: 10.1210/jcem-70-4-983.

Abstract

To investigate the regulation of the synthesis and secretion of placental proteins-12 (PP12) and -14 (PP14) and PRL, explants and enriched preparations of stromal cells and gland cells obtained from 10 human early pregnancy decidua were preincubated in medium for 24 h (baseline), followed by incubation in medium with or without progesterone (0.02-32 mumol/L), hCG (10 and 100 ng/ml), or cAMP (0.25-1 mmol/L) in an atmosphere of 5% CO2-95% air at 37 C for another 96-120 h. Media were changed each 24 h, and PP12, PP14, and PRL levels were determined by RIA. Decidual explants, as well as their isolated cells produced detectable levels of PP12, PP14, and PRL in vitro. The gland cells synthesized and secreted about 30 times more PP14 than did stromal cells. After 96-120 h of incubation, the production of each protein by control cultures was increased 81-167% compared to the baseline (not significant). The secretion of these proteins in medium supplemented with progesterone or hCG was not significantly different from that in the control groups. 8-Bromo-cAMP significantly increased the secretion of PRL and PP12, but not PP14, by stromal cells compared to control values. We conclude that 1) PP14 is mainly produced by decidual gland cells; 2) progesterone at the concentrations used in our study does not stimulate production of PP12, PP14, and PRL in decidualized endometrium in vitro; 3) hCG does not stimulate the production of PP12 and PP14 in decidualized endometrium; and 4) 8-bromo-cAMP stimulates decidual stromal cell secretion of PRL and PP12.

摘要

为研究胎盘蛋白-12(PP12)、胎盘蛋白-14(PP14)和催乳素(PRL)合成与分泌的调节机制,从10例人类早孕蜕膜获取的基质细胞和腺细胞外植体及富集制剂先在培养基中预孵育24小时(基线),然后在含或不含孕酮(0.02 - 32 μmol/L)、人绒毛膜促性腺激素(hCG,10和100 ng/ml)或环磷酸腺苷(cAMP,0.25 - 1 mmol/L)的培养基中,于37℃、5%二氧化碳 - 95%空气环境下再孵育96 - 120小时。每24小时更换一次培养基,采用放射免疫分析法(RIA)测定PP12、PP14和PRL水平。蜕膜外植体及其分离的细胞在体外可产生可检测水平的PP12、PP14和PRL。腺细胞合成和分泌的PP14比基质细胞多约30倍。孵育96 - 120小时后,对照培养物中每种蛋白质的产量与基线相比增加了81 - 167%(无显著差异)。在补充孕酮或hCG的培养基中这些蛋白质的分泌与对照组相比无显著差异。与对照值相比,8 - 溴 - cAMP显著增加了基质细胞PRL和PP12的分泌,但未增加PP14的分泌。我们得出以下结论:1)PP14主要由蜕膜腺细胞产生;2)我们研究中所用浓度的孕酮在体外不刺激蜕膜化子宫内膜中PP12、PP14和PRL的产生;3)hCG不刺激蜕膜化子宫内膜中PP12和PP14的产生;4)8 - 溴 - cAMP刺激蜕膜基质细胞分泌PRL和PP12。

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