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着床前因子调节人子宫内膜基质细胞的整个蜕膜化过程中的滋养细胞浸润。

Preimplantation factor modulates trophoblastic invasion throughout the decidualization of human endometrial stromal cells.

机构信息

Université Paris-Saclay, UVSQ, INRAE, BREED, F-78350, Jouy-en-Josas, France.

Ecole Nationale Vétérinaire d'Alfort, BREED, F-94700, Maisons-Alfort, France.

出版信息

Reprod Biol Endocrinol. 2021 Jun 27;19(1):96. doi: 10.1186/s12958-021-00774-5.

Abstract

BACKGROUND

Successful human embryo implantation requires the differentiation of endometrial stromal cells (ESCs) into decidual cells during a process called decidualization. ESCs express specific markers of decidualization, including prolactin, insulin-like growth factor-binding protein-1 (IGFBP-1), and connexin-43. Decidual cells also control of trophoblast invasion by secreting various factors, such as matrix metalloproteinases (MMPs) and tissue inhibitors of metalloproteinases. Preimplantation factor (PIF) is a recently identified, embryo-derived peptide with activities at the fetal-maternal interface. It creates a favorable pro-inflammatory environment in human endometrium and directly controls placental development by increasing the human trophoblastic cells' ability to invade the endometrium. We hypothesized that PIF's effects on the endometrium counteract its pro-invasive effects.

METHODS

We tested sPIF effect on the expression of three decidualization markers by RT-qPCR and/or immunochemiluminescence assay. We examined sPIF effect on human ESC migration by performing an in vitro wound healing assay. We analyzed sPIF effect on endometrial control of human trophoblast invasion by performing a zymography and an invasion assay.

RESULTS

Firstly, we found that a synthetic analog of PIF (sPIF) significantly upregulates the mRNA expression of IGFBP-1 and connexin-43, and prolactin secretion in ESCs - suggesting a pro-differentiation effect. Secondly, we showed that the HTR-8/SVneo trophoblastic cell line's invasive ability was low in the presence of conditioned media from ESCs cultured with sPIF. Thirdly, this PIF's anti-invasive action was associated with a specifically decrease in MMP-9 activity.

CONCLUSION

Taken as a whole, our results suggest that PIF accentuates the decidualization process and the production of endometrial factors that limit trophoblast invasion. By controlling both trophoblast and endometrial cells, PIF therefore appears to be a pivotal player in the human embryo implantation process.

摘要

背景

成功的胚胎着床需要子宫内膜基质细胞(ESCs)在蜕膜化过程中分化为蜕膜细胞。ESCs 表达蜕膜化的特定标志物,包括催乳素、胰岛素样生长因子结合蛋白-1(IGFBP-1)和连接蛋白-43。蜕膜细胞还通过分泌各种因子来控制滋养层细胞的侵袭,如基质金属蛋白酶(MMPs)和金属蛋白酶组织抑制剂。植入前因子(PIF)是一种最近发现的、胚胎来源的肽,在胎儿-母体界面具有活性。它在人子宫内膜中创造了一个有利的促炎环境,并通过增加人滋养层细胞侵袭子宫内膜的能力直接控制胎盘发育。我们假设 PIF 对子宫内膜的作用抵消了其促侵袭作用。

方法

我们通过 RT-qPCR 和/或免疫化学发光法检测 sPIF 对三种蜕膜化标志物表达的影响。我们通过体外划痕愈合实验检测 sPIF 对人 ESC 迁移的影响。我们通过进行酶谱和侵袭实验分析 sPIF 对子宫内膜控制人滋养层细胞侵袭的影响。

结果

首先,我们发现 PIF 的合成类似物(sPIF)显著上调了 ESCs 中 IGFBP-1 和连接蛋白-43 的 mRNA 表达,以及催乳素的分泌-提示具有促分化作用。其次,我们表明,在含有 sPIF 培养的 ESCs 条件培养基存在的情况下,HTR-8/SVneo 滋养层细胞系的侵袭能力较低。第三,这种 PIF 的抗侵袭作用与 MMP-9 活性的特异性降低有关。

结论

总的来说,我们的结果表明,PIF 强调了蜕膜化过程和子宫内膜因子的产生,这些因子限制了滋养层细胞的侵袭。通过控制滋养层细胞和子宫内膜细胞,PIF 似乎是人类胚胎着床过程中的关键参与者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f5b/8237507/f8e700faa802/12958_2021_774_Fig1_HTML.jpg

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