整合素和配体,在怀孕期间与猪胎盘界面是否相关?

Carolina Vélez, Mariángeles Clauzure, Delia Williamson, Mónica García, Mirta Koncurat, Claudio Barbeito
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摘要

在本研究中,我们重点研究了不同妊娠期猪胎盘界面的整合素及其受体。研究对象为妊娠 17、30、60 和 70 dg 的杂交母猪子宫胎盘界面(n=24)和非妊娠子宫(n=4)。采用免疫组织化学方法检测αvβ3和α5β1整合素及其配体纤维连接蛋白(FN)和骨生长因子(OPN)的存在,并测定免疫标记面积百分比(IAP)和光密度(OD)。所分析的整合素及其配体在妊娠早期和中期出现了表达高峰,在妊娠 70 dg 时,IAP 和 OD 面积均有所下降。这些时间上的变化向我们表明,这项工作中研究的分子参与了胚胎/胎儿与母体的附着,而且是可变的。此外,我们发现滋养层 FN 和子宫内膜 αvβ3、滋养层 OPN 和子宫内膜 α5β1的免疫染色的强度和范围在整个猪妊娠过程中都有显著的相关性。在妊娠晚期,胎盘会发生明显的重塑,随后子宫胎盘界面的褶皱会被去除或更新,从而导致局灶性粘连的消失。在妊娠晚期,特别是 70 dg 时,一些整合素及其配体的表达减少,这表明可能还有其他粘附分子和配体参与母胎界面的建立。
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Integrins and ligands, are correlated at pig placental interface during pregnancy?

In the present work, we emphasize the studies about integrins and their receptors in pig placental interface at different times of gestation. Uterine placental interface (n=24) of 17-, 30-, 60- and 70-days gestation (dg) and non-pregnant uterus (n=4) of crossbred sows were used. The presence of αvβ3 and α5β1 integrins, and their ligands fibronectin (FN), and osteopontin (OPN) were detected by immunohistochemistry, and the immunolabelled area percentage (IAP) and the optical density (OD) were determined. The integrins and its ligands analyzed have presented peaks of expression in early and mid-gestation, both in IAP and the OD area decreasing at 70 dg. These temporal changes showed us that the molecules studied in this work participate in embryo/feto-maternal attachment, variably. Besides, we found a significant correlation both in the intensity and in the extension of immunostaining for trophoblastic FN and endometrial αvβ3, and trophoblastic OPN and endometrial α5β1, throughout the entire pig pregnancy. At late gestation, take place a notable placental remodelation with subsequent removal or renewal of folds at the uterine-placental interface that results in the loss of focal adhesions. The decrease of the expression of some integrins and their ligands in late gestation, particularly at 70 dg, would demonstrate that there would be other adhesion molecules and other ligands that could be participating in the establishment of the maternal-fetal interface.

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