Boeddeker Sarah Jean, Baston-Buest Dunja Maria, Fehm Tanja, Kruessel Jan, Hess Alexandra
Department of Obstetrics/Gynecology and Reproductive Endocrinology and Infertility (UniKiD), Medical Center University of Duesseldorf, Duesseldorf, Germany.
Department of Obstetrics and Gynecology, Medical Center University of Duesseldorf, Duesseldorf, Germany.
PLoS One. 2015 Apr 1;10(4):e0121103. doi: 10.1371/journal.pone.0121103. eCollection 2015.
Human embryo invasion and implantation into the inner wall of the maternal uterus, the endometrium, is the pivotal process for a successful pregnancy. Whereas disruption of the endometrial epithelial layer was already correlated with the programmed cell death, the role of apoptosis of the subjacent endometrial stromal cells during implantation is indistinct. The aim was to clarify whether apoptosis plays a role in the stromal invasion and to characterize if the apoptotic susceptibility of endometrial stromal cells to embryonic stimuli is influenced by decidualization and Syndecan-1. Therefore, the immortalized human endometrial stromal cell line St-T1 was used to first generate a new cell line with a stable Syndecan-1 knock down (KdS1), and second to further decidualize the cells with progesterone. As a replacement for the ethically inapplicable embryo all cells were treated with the embryonic factors and secretion products interleukin-1β, interferon-γ, tumor necrosis factor-α, transforming growth factor-β1 and anti-Fas antibody to mimic the embryo contact. Detection of apoptosis was verified via Caspase ELISAs, PARP cleavage and Annexin V staining. Apoptosis-related proteins were investigated via antibody arrays and underlying signaling pathways were analyzed by Western blot. Non-decidualized endometrial stromal cells showed a resistance towards apoptosis which was rescinded by decidualization and Syndecan-1 knock down independent of decidualization. This was correlated with an altered expression of several pro- and anti-apoptotic proteins and connected to a higher activation of pro-survival Akt in non-differentiated St-T1 as an upstream mediator of apoptotis-related proteins. This study provides insight into the largely elusive process of implantation, proposing an important role for stromal cell apoptosis to successfully establish a pregnancy. The impact of Syndecan-1 in attenuating the apoptotic signal is particularly interesting in the light of an already described influence on pregnancy disorders and therefore might provide a useful clinical tool in the future to prevent pregnancy complications provoked by inadequate implantation.
人类胚胎侵入并植入母体子宫内壁即子宫内膜,是成功妊娠的关键过程。虽然子宫内膜上皮层的破坏已与程序性细胞死亡相关,但植入过程中相邻子宫内膜基质细胞凋亡的作用尚不清楚。本研究旨在阐明凋亡是否在基质侵入中发挥作用,并确定子宫内膜基质细胞对胚胎刺激的凋亡易感性是否受蜕膜化和Syndecan-1的影响。因此,使用永生化的人子宫内膜基质细胞系St-T1,首先生成一种稳定敲低Syndecan-1(KdS1)的新细胞系,其次用孕酮使细胞进一步蜕膜化。作为伦理上不可用的胚胎的替代物,所有细胞均用胚胎因子和分泌产物白细胞介素-1β、干扰素-γ、肿瘤坏死因子-α、转化生长因子-β1和抗Fas抗体处理,以模拟胚胎接触。通过半胱天冬酶酶联免疫吸附测定、聚(ADP-核糖)聚合酶切割和膜联蛋白V染色验证凋亡检测。通过抗体阵列研究凋亡相关蛋白,并通过蛋白质印迹分析潜在的信号通路。未蜕膜化的子宫内膜基质细胞对凋亡具有抗性,这种抗性通过蜕膜化和Syndecan-1敲低(与蜕膜化无关)而消除。这与几种促凋亡和抗凋亡蛋白的表达改变相关,并与未分化的St-T1中作为凋亡相关蛋白上游介质的促生存Akt的更高激活有关。本研究深入了解了在很大程度上难以捉摸的植入过程,提出基质细胞凋亡在成功建立妊娠中起重要作用。鉴于Syndecan-1对妊娠疾病的影响已被描述,其在减弱凋亡信号方面的作用尤其有趣,因此可能在未来提供一种有用的临床工具,以预防因植入不足引起的妊娠并发症。