Lee Chang-Jin, Hong Seon-Hwa, Yoon Min-Ji, Lee Kyung-Ah, Ko Jung-Jae, Koo Hwa Seon, Kim Jee Hyun, Choi Dong Hee, Kwon Hwang, Kang Youn-Jung
Department of Biomedical Science, School of Life Science, CHA University, Seongnam, Korea.
CHA Fertility Center Bundang, CHA University, Seongnam, Korea.
Clin Exp Reprod Med. 2020 Jun;47(2):114-121. doi: 10.5653/cerm.2019.03454. Epub 2020 May 29.
Despite extensive research on implantation failure, little is known about the molecular mechanisms underlying the crosstalk between the embryo and the maternal endometrium, which is critical for successful pregnancy. Profilin 1 (PFN1), which is expressed both in the embryo and in the endometrial epithelium, acts as a potent regulator of actin polymerization and the cytoskeletal network. In this study, we identified the specific role of endometrial PFN1 during embryo implantation.
Morphological alterations depending on the status of PFN1 expression were assessed in PFN1-depleted or control cells grown on Matrigel-coated cover glass. Day-5 mouse embryos were cocultured with Ishikawa cells. Comparisons of the rates of F-actin formation and embryo attachment were performed by measuring the stability of the attached embryo onto PFN1-depleted or control cells.
Depletion of PFN1 in endometrial epithelial cells induced a significant reduction in cell-cell adhesion displaying less formation of colonies and a more circular cell shape. Mouse embryos co-cultured with PFN1-depleted cells failed to form actin cytoskeletal networks, whereas more F-actin formation in the direction of surrounding PFN1-intact endometrial epithelial cells was detected. Furthermore, significantly lower embryo attachment stability was observed in PFN1-depleted cells than in control cells. This may have been due to reduced endometrial receptivity caused by impaired actin cytoskeletal networks associated with PFN1 deficiency.
These observations definitively demonstrate an important role of PFN1 in mediating cell-cell adhesion during the initial stage of embryo implantation and suggest a potential therapeutic target or novel biomarker for patients suffering from implantation failure.
尽管对植入失败进行了广泛研究,但对于胚胎与母体子宫内膜之间相互作用的分子机制仍知之甚少,而这种相互作用对成功妊娠至关重要。肌动蛋白结合蛋白1(PFN1)在胚胎和子宫内膜上皮中均有表达,是肌动蛋白聚合和细胞骨架网络的有效调节因子。在本研究中,我们确定了子宫内膜PFN1在胚胎植入过程中的具体作用。
在包被基质胶的盖玻片上培养的PFN1缺失细胞或对照细胞中,评估取决于PFN1表达状态的形态学改变。将第5天的小鼠胚胎与 Ishikawa 细胞共培养。通过测量附着在PFN1缺失细胞或对照细胞上的胚胎的稳定性,对F-肌动蛋白形成率和胚胎附着率进行比较。
子宫内膜上皮细胞中PFN1的缺失导致细胞间黏附显著减少,表现为集落形成减少和细胞形状更圆。与PFN1缺失细胞共培养的小鼠胚胎未能形成肌动蛋白细胞骨架网络,而在周围PFN1完整的子宫内膜上皮细胞方向检测到更多的F-肌动蛋白形成。此外,观察到PFN1缺失细胞中的胚胎附着稳定性明显低于对照细胞。这可能是由于与PFN1缺乏相关的肌动蛋白细胞骨架网络受损导致子宫内膜容受性降低。
这些观察结果明确证明了PFN1在胚胎植入初始阶段介导细胞间黏附中的重要作用,并为植入失败的患者提出了潜在的治疗靶点或新型生物标志物。