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Isolation and Purification of an Early Pregnancy Factor–Like Molecule from Culture Supernatants Obtained from Lymphocytes of Pregnant Women

机译:从孕妇淋巴细胞培养上清液中分离和纯化早期妊娠因子样分子

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摘要

>Purpose:Our purpose was to determine whether lymphocytes synthesize proteins during pregnancy, to observe whether one of the proteins synthesized has early pregnancy factor (EPF)–like activity and to isolate and purify this molecule from culture supernatants obtained from stimulated lymphocytes of pregnant women.>Methods:Lymphocyte proliferation assay and35S-methionine labeling were done to study de novo synthesis of proteins followed by autoradiography to confirm synthesis of proteins. The rosette inhibition assay was used for detection of the EPF-like molecule. Gel filtration on Sephadex G-100 and RPHPLC were used for purification of the EPF-like molecule.>Results:The rate of incorporation of35S-methionine was significantly higher in the lymphocytes of pregnant women compared to those of the control, and autoradiography confirmed the synthesis of proteins during pregnancy. There is a total protein enhancement trend observed during the first trimester that declines toward term. The EPF-like molecule is observed to be synthesized during all the trimesters of pregnancy. This molecule, when purified, showed a single homogeneous biologically active peak.>Conclusions:The results indicated that there is an enhancement of existing protein or synthesis of new proteins during pregnancy. The EPF-like molecule is one of the many proteins synthesized and secreted by lymphocytes during pregnancy that, when purified, is biologically active.
机译:>目的:我们的目的是确定妊娠期间淋巴细胞是否合成蛋白质,观察其中一种合成蛋白质是否具有早期妊娠因子(EPF)样活性,并从获得的培养上清液中分离和纯化该分子>方法:通过淋巴细胞增殖测定和 35 S-蛋氨酸标记来研究蛋白质的从头合成,然后进行放射自显影以确认蛋白质的合成。玫瑰花结抑制测定法用于检测EPF样分子。 >结果 35 S-蛋氨酸的掺入率显着提高,采用Sephadex G-100凝胶过滤和RPHPLC纯化EPF样分子。孕妇的淋巴细胞与对照组相比,放射自显影证实了怀孕期间蛋白质的合成。在头三个月期间观察到总蛋白增强趋势,该趋势朝足月下降。观察到EPF样分子在怀孕的所有三个月中都是合成的。纯化后,该分子显示出一个单一的均一的生物活性峰。>结论:结果表明,怀孕期间现有蛋白质的增强或新蛋白质的合成。 EPF样分子是怀孕期间淋巴细胞合成和分泌的许多蛋白质之一,纯化后具有生物活性。

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