前列腺素 E₂ 通过前列腺素 E₂ 受体(PTGER2)在胚胎植入过程中对滋养层/胚胎细胞的自分泌和旁分泌作用机制。

Autocrine and paracrine mechanisms of prostaglandin E₂ action on trophoblast/conceptus cells through the prostaglandin E₂ receptor (PTGER2) during implantation.

机构信息

Institute of Animal Reproduction and Food Research of Polish Academy of Sciences, Tuwima 10, 10-748 Olsztyn, Poland.

出版信息

Endocrinology. 2013 Oct;154(10):3864-76. doi: 10.1210/en.2012-2271. Epub 2013 Jul 16.

Abstract

The conceptus and endometrium secrete large amounts of prostaglandin E₂ (PGE₂) into the porcine uterine lumen during the periimplantation period. We hypothesized that PGE₂ acts on conceptus/trophoblast cells through auto- and paracrine mechanisms. Real-time RT-PCR analysis revealed that PGE₂ receptor (PTGER)2 mRNA was 14-fold greater in conceptuses/trophoblasts on days 14-25 (implantation and early placentation period) vs preimplantation day 10-13 conceptuses (P < .05). Similarly, expression of PTGER2 protein increased during implantation. Conceptus expression of PTGER4 mRNA and protein did not differ on days 10-19. PGE₂ stimulated PTGER2 mRNA expression in day 15 trophoblast cells through PTGER2 receptor signaling. PGE₂ elevated aromatase expression and estradiol-17β secretion by trophoblast cells. Moreover, PGE₂ and the PTGER2 agonist, butaprost, increased the adhesive capacity of both human HTR-8/SVneo trophoblast and primary porcine trophoblast cells to extracellular matrix. This PGE₂-induced alteration in trophoblast cell adhesion to extracellular matrix was abolished by incubation of these cells with AH6809 (PTGER2 antagonist), ITGAVB3-directed tetrapeptide arg-gly-asp-ser or integrin ITGAVB3 antibody. PGE₂ stimulated adhesion of porcine trophoblast cells via the estrogen receptor and MEK/MAPK signaling pathway. PGE₂ induced phosphorylation of MAPK1/MAPK3 through PTGER2 and up-regulated expression of cell adhesion proteins such as focal adhesion kinase and intercellular adhesion molecule-1. Our study indicates that elevated PGE₂ in the periimplantation uterine lumen stimulates conceptus PTGER2 expression, which in turn promotes trophoblast adhesion via integrins, and synthesis and secretion of the porcine embryonic signal estradiol-17β. Moreover, the mechanism through which PGE₂ increases trophoblast adhesion is not species specific because it is PTGER2- and integrin-dependent in both porcine and human trophoblast cells.

摘要

在着床期,胚泡和子宫内膜会向猪子宫腔分泌大量前列腺素 E₂(PGE₂)。我们假设 PGE₂ 通过自分泌和旁分泌机制作用于胚泡/滋养层细胞。实时 RT-PCR 分析显示,在着床和早期胎盘形成期(第 14-25 天),胚泡/滋养层中的 PGE₂ 受体(PTGER)2 mRNA 是第 10-13 天胚泡(植入前)的 14 倍(P<.05)。同样,PTGER2 蛋白的表达在着床期间增加。在第 10-19 天,胚泡表达的 PTGER4 mRNA 和蛋白没有差异。PGE₂ 通过 PTGER2 受体信号刺激第 15 天滋养层细胞中 PTGER2 mRNA 的表达。PGE₂ 升高滋养层细胞中芳香酶的表达和雌二醇-17β 的分泌。此外,PGE₂ 和 PTGER2 激动剂,butaprost,增加了人 HTR-8/SVneo 滋养层和原代猪滋养层细胞对细胞外基质的黏附能力。用 AH6809(PTGER2 拮抗剂)、ITGAVB3 导向四肽精氨酸-甘氨酸-天冬氨酸-丝氨酸或整合素 ITGAVB3 抗体孵育这些细胞,可消除 PGE₂ 诱导的滋养层细胞对细胞外基质黏附的改变。PGE₂ 通过雌激素受体和 MEK/MAPK 信号通路刺激猪滋养层细胞的黏附。PGE₂ 通过 PTGER2 诱导 MAPK1/MAPK3 的磷酸化,并上调细胞黏附蛋白如粘着斑激酶和细胞间黏附分子-1 的表达。我们的研究表明,着床期子宫腔中升高的 PGE₂ 刺激胚泡 PTGER2 的表达,进而通过整合素促进滋养层细胞的黏附,并合成和分泌猪胚胎信号雌二醇-17β。此外,PGE₂ 增加滋养层细胞黏附的机制不是种属特异性的,因为它在猪和人滋养层细胞中均依赖于 PTGER2 和整合素。

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