Herrler Andreas, von Rango Ulrike, Beier Henning M
Department of Anatomy and Reproductive Biology, Medical School, RWTH University of Aachen, 52074 Aachen, Germany.
Reprod Biomed Online. 2003 Mar;6(2):244-56. doi: 10.1016/s1472-6483(10)61717-8.
The process of implantation and trophoblast invasion is currently considered as the most limiting factor for the establishment of pregnancy. Molecular interactions at the embryo-maternal interface during the time of adhesion and subsequent invasion are crucial to the process of embryonic implantation. Both partners, the mother as well as the embryo, play equal roles in the embryo-maternal dialogue, the embryonic part being the main topic in this study. Investigations of the proteins in the extra-embryonic matrices (i.e. zona pellucida) indicate that the embryo participates intensively in this early embryo-maternal signalling. One unique feature during implantation process of primate embryos is the release of chorionic gonadotrophin, which seems to influence endometrial activity by two different mechanisms: (i) luteotrophic activity with increasing progesterone release and (ii) a direct action on the endometrium. Furthermore, embryonic interleukin-1beta may be involved in embryo-maternal signalling. Other significant signals in this interaction are most likely leukaemia inhibitory factor (LIF) and colony-stimulating factor (CSF), which stimulate matrix metalloproteinase (MMP)/insulin-like growth factor binding protein-1 (IGFBP-1) activity and the insulin-like growth factor (IGF) system, which is modulated by embryonic IGFBP-3. Similar significances are discussed for uteroglobin and haptoglobin. Finally, the phenomenon of maternal immunological tolerance, triggered by the presence of the early embryo, is fundamental to the understanding of implantation and trophoblast invasion. A tightly regulated balance between activated and inactivated T cells at the implantation site may control the beginning of adequate trophoblast invasion and also limit this invasion to a tolerable extent for the maternal system, consequently ensuring a biologically healthy haemo-chorial placenta.
目前认为,着床和滋养层细胞侵入过程是妊娠建立的最限制因素。在黏附及随后侵入期间,胚胎-母体界面处的分子相互作用对胚胎着床过程至关重要。母体和胚胎这两个参与者在胚胎-母体对话中发挥着同等作用,胚胎部分是本研究的主要主题。对胚外基质(即透明带)中的蛋白质进行的研究表明,胚胎在这种早期胚胎-母体信号传导中发挥着积极作用。灵长类胚胎着床过程中的一个独特特征是绒毛膜促性腺激素的释放,它似乎通过两种不同机制影响子宫内膜活性:(i)促黄体活性,随着孕酮释放增加;(ii)对子宫内膜的直接作用。此外,胚胎白细胞介素-1β可能参与胚胎-母体信号传导。这种相互作用中的其他重要信号很可能是白血病抑制因子(LIF)和集落刺激因子(CSF),它们刺激基质金属蛋白酶(MMP)/胰岛素样生长因子结合蛋白-1(IGFBP-1)活性,以及由胚胎IGFBP-3调节的胰岛素样生长因子(IGF)系统。子宫珠蛋白和触珠蛋白也有类似的重要意义。最后,由早期胚胎的存在引发的母体免疫耐受现象,对于理解着床和滋养层细胞侵入至关重要。着床部位活化和失活T细胞之间严格调控的平衡可能控制着适当的滋养层细胞侵入的开始,并将这种侵入限制在母体系统可耐受的范围内,从而确保形成生物学上健康的血绒毛膜胎盘。