Department of Obstetrics and Gynecology, Cathay General Hospital, Taipei, Taiwan; School of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
Ph.D. Program in Biopharmaceutical Biotechnology, College of Medicine, Fu Jen Catholic University, New Taipei City, Taiwan.
J Reprod Immunol. 2022 Aug;152:103650. doi: 10.1016/j.jri.2022.103650. Epub 2022 Jun 6.
In humans, successful implantation requires a finely tuned synchrony between an appropriately developing embryo and the receptive endometrium, involving apposition, adhesion, and invasion. Therefore, this study was sought to establish a coculture cell model to investigate trophoblast-mediated blastocyst apposition and adhesion to endometrial epithelium events during embryo implantation. The direct contact and indirect noncontact coculture models were successfully established by using human BeWo trophoblasts and HEC-1A endometrial epithelial cells. Interestingly, a significant increase of ICAM-1 protein and mRNA expression was observed in both coculture systems when challenged with follicle-stimulating factor (FSH). In accordance with these observations, trophoblast-conditioned medium (CM) could also enhance epithelial ICAM-1 production, suggesting involvement of trophoblast-secreting factor(s) in crosstalk between two cells. Indeed, FSH stimulation enhanced TNF-α expression in the trophoblasts and epithelial ICAM-1 induction were abolished by a TNF-α blocking/neutralizing antibody (TNF-α B/N Ab). Meanwhile, the intracellular calcium, PKA/CREB, and transcription/translation signaling pathways in epithelial cells participated in the ICAM-1 induction. Finally, the trophoblast cells were more susceptible to adhesion to CM-primed epithelial cell monolayer, where the adhesion could be abolished by TNF-α B/N Ab. Therefore, we present here novel findings that coculture of trophoblast with endometrial epithelial cells in the presence of FSH leads to an increase in epithelial ICAM-1 expression and trophoblast adhesion to epithelial monolayer through stimulating trophoblast's TNF-α cytokine production. This study also addresses an important issue that a possible role of microenvironmental and exogenously-added FSH in enhancing blastocyst interaction with endometrium during embryo implantation of natural or in-vitro fertilization cycle.
在人类中,成功的着床需要胚胎的适当发育与接受性子宫内膜之间的精细同步,涉及贴附和侵入。因此,本研究旨在建立一种共培养细胞模型,以研究胚胎着床过程中滋养层介导的囊胚贴附和黏附到子宫内膜上皮的事件。通过使用人 BeWo 滋养层细胞和 HEC-1A 子宫内膜上皮细胞,成功建立了直接接触和间接非接触共培养模型。有趣的是,当受到卵泡刺激素(FSH)刺激时,两种共培养系统中 ICAM-1 蛋白和 mRNA 的表达均显著增加。与这些观察结果一致,滋养层条件培养基(CM)也可以增强上皮细胞 ICAM-1 的产生,这表明滋养层分泌的因子(s)参与了两细胞之间的串扰。事实上,FSH 刺激增强了滋养层细胞中 TNF-α 的表达,而 TNF-α 阻断/中和抗体(TNF-α B/N Ab)消除了上皮细胞中 ICAM-1 的诱导。同时,上皮细胞中的细胞内钙、PKA/CREB 和转录/翻译信号通路参与了 ICAM-1 的诱导。最后,滋养层细胞更容易黏附到 CM 预激活的上皮细胞单层上,而 TNF-α B/N Ab 可以消除这种黏附。因此,我们在这里提出了新的发现,即在 FSH 存在下,滋养层与子宫内膜上皮细胞共培养会导致上皮细胞 ICAM-1 表达增加,滋养层黏附到上皮细胞单层,而 TNF-α B/N Ab 可以消除这种黏附。这项研究还解决了一个重要问题,即在自然或体外受精周期中,微环境和外源性添加的 FSH 可能在增强囊胚与子宫内膜的相互作用方面发挥作用。