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糖蛋白A与孕早期滋养层细胞的体外分化

Glycodelin A and differentiation of first trimester trophoblast cells in vitro.

作者信息

Jeschke U, Richter D-U, Reimer T, Bergemann C, Briese V, Karsten U, Mylonas I, Kupka M S, Wiest I, Friese K

机构信息

First Department of Obstetrics and Gynecology, Ludwig Maximilians University of Munich, Maistrasse 11, 80337, Munich, Germany.

出版信息

Arch Gynecol Obstet. 2005 Jul;272(2):151-9. doi: 10.1007/s00404-004-0682-2. Epub 2004 Nov 10.

Abstract

AIM

The glycoprotein, glycodelin A (GdA) is a main product of the maternal decidua in the first trimester of pregnancy and is secreted into the amniotic fluid. The purpose of this study was to investigate the effect of GdA on secretion and surface markers of isolated first trimester trophoblasts in vitro.

METHODS

Cytotrophoblasts were prepared from human first trimester placentae and incubated with varying concentrations of GdA or transfected separately with the expression plasmid of GdA. Supernatants were assayed for human chorionic gonadotropin (hCG) protein concentrations. Expression of human placental lactogen (hPL), mucin 1 (MUC1) and the Thomsen-Friedenreich (TF) epitope was analysed in stimulated trophoblast cells and in unstimulated controls by immunocytochemistry.

RESULTS

Glycodelin A induced a reduced expression of hPL compared with unstimulated controls. Expression of MUC1 was not affected by GdA. Freshly isolated trophoblast cells showed no TF expression but became positive for this antigen after 96 h of cultivation. GdA-stimulated trophoblast cells inhibited TF expression after 96 h of cultivation. GdA plasmids induced a significantly higher hCG production in transfected cells than in cells transfected with the empty plasmid.

CONCLUSIONS

The results obtained in this study suggest that GdA is involved in the differentiation of trophoblast cells. The treatment of GdA plasmid transfected trophoblast cells stimulated hCG production in isolated trophoblast cells and inhibited hPL and TF expression, suggesting a functional link between hCG and GdA.

摘要

目的

糖蛋白糖萼素A(GdA)是孕早期母体蜕膜的主要产物,并分泌到羊水中。本研究的目的是在体外研究GdA对分离的孕早期滋养层细胞分泌及表面标志物的影响。

方法

从人孕早期胎盘制备细胞滋养层细胞,并用不同浓度的GdA孵育,或分别用GdA表达质粒转染。检测上清液中人绒毛膜促性腺激素(hCG)蛋白浓度。通过免疫细胞化学分析在受刺激的滋养层细胞和未受刺激的对照中人类胎盘催乳素(hPL)、黏蛋白1(MUC1)和桑福德-弗里德赖希(TF)表位的表达。

结果

与未受刺激的对照相比,糖萼素A诱导hPL表达降低。GdA不影响MUC1的表达。新鲜分离的滋养层细胞未显示TF表达,但培养96小时后该抗原呈阳性。培养96小时后,GdA刺激的滋养层细胞抑制TF表达。GdA质粒转染的细胞比空质粒转染的细胞诱导产生显著更高的hCG。

结论

本研究结果表明,GdA参与滋养层细胞的分化。用GdA质粒转染滋养层细胞可刺激分离的滋养层细胞产生hCG,并抑制hPL和TF表达,提示hCG与GdA之间存在功能联系。

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