KLF4 regulates trophoblast function and associates with unexplained recurrent spontaneous abortion.

IF 5.3 2区 材料科学 Q2 MATERIALS SCIENCE, MULTIDISCIPLINARY
Yiling Tan, Jiayu Wang, Chunming Liu, Shujuan Wu, Mengqi Zhou, Yan Zhang, Tailang Yin, Jing Yang
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引用次数: 0

Abstract

Background: Recurrent spontaneous abortion (RSA) is defined as two or more consecutive spontaneous abortions before 20 weeks with the same spouse [1]. However, approximately 50% of RSA cases of unknown cause are classified as unexplained recurrent spontaneous abortion (URSA). Potential factors include decreased trophoblast cell migration and invasion, leading to impaired placental implantation and maintenance of the normal maternal-fetal interface. However, the mechanism of this pathogenesis remains unknown. In this study, we investigated the potential role and mechanism of KLF4 in regulating URSA by influencing the invasion and migration ability of trophoblast cells.

Methods: We firstly identified 817 differentially expressed genes by performing a difference analysis of the dataset GSE121950 [2] related to recurrent abortion, and intersected the top 10 genes obtained respectively by the three algorithms: DMNC, MNC, and EPC using Venn Diagram.To detect the expression levels of core genes, villi samples were obtained from normal pregnant women and patients with URSA. RT-qPCR analysis revealed a significant difference in KLF4 mRNA expression and KLF4 was then analyzed. Trophoblast cell lines HTR8 and JEG3 were used to investigate the effect of KLF4 on trophoblastic function. Wound healing and transwell assays was performed to detect the invasion and migration of trophoblast cells. The expression of epithelial-mesenchymal transition(EMT) molecules were detected by RT-qPCR and western blot. Promoter detection and epigenetic modification were detected by chromatin immunoprecipitation (ChIP) assay. Molecular nuclear localization was detected by immunofluorescence and subcellular fractionation. Miscarried mice model was used to study the effects of KLF4 on URSA induced by reduced trophoblast invasion and migration.

Results: KLF4 is highly expressed in the villi of patients with URSA. KLF4 inhibits the expression level of H3R2ME2a in trophoblast cells by regulating the transcriptional level and nuclear translocation of PRMT6, thereby inhibiting the possible regulatory mechanism of trophoblastic invasion and providing a potential treatment strategy for URSA in vivo.

Conclusions: The KLF4/PRMT6/H3R2ME2a axis regulates mechanisms associated with unexplained recurrent spontaneous abortion by regulating trophoblast function.

KLF4调节滋养细胞的功能,并与原因不明的复发性自然流产有关。
背景:复发性自然流产(RSA)是指同一配偶在 20 周前连续两次或两次以上自然流产[1]。然而,约 50%原因不明的 RSA 病例被归类为原因不明的复发性自然流产(URSA)。潜在的因素包括滋养层细胞迁移和入侵减少,导致胎盘植入和正常母胎界面的维持受损。然而,这种发病机制仍然未知。本研究探讨了KLF4通过影响滋养层细胞的侵袭和迁移能力来调控URSA的潜在作用和机制:首先,我们通过对与复发性流产相关的数据集 GSE121950 [2]进行差异分析,确定了 817 个差异表达基因,并将三种算法分别得到的前 10 个基因进行交叉:为了检测核心基因的表达水平,研究人员从正常孕妇和URSA患者身上采集了绒毛样本。RT-qPCR 分析显示 KLF4 mRNA 表达存在显著差异,因此对 KLF4 进行了分析。滋养层细胞株 HTR8 和 JEG3 被用来研究 KLF4 对滋养层功能的影响。伤口愈合和跨孔试验用于检测滋养层细胞的侵袭和迁移。通过RT-qPCR和Western印迹检测上皮-间质转化(EMT)分子的表达。通过染色质免疫沉淀(ChIP)检测启动子和表观遗传修饰。通过免疫荧光和亚细胞分馏检测分子核定位。利用流产小鼠模型研究 KLF4 对滋养细胞侵袭和迁移减少诱导的 URSA 的影响:结果:KLF4在URSA患者的绒毛中高表达。KLF4通过调节PRMT6的转录水平和核转位,抑制滋养层细胞中H3R2ME2a的表达水平,从而抑制滋养层细胞侵袭的可能调控机制,为体内URSA提供了一种潜在的治疗策略:结论:KLF4/PRMT6/H3R2ME2a轴通过调控滋养细胞的功能调节不明原因复发性自然流产的相关机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.30
自引率
3.40%
发文量
1601
期刊介绍: ACS Applied Nano Materials is an interdisciplinary journal publishing original research covering all aspects of engineering, chemistry, physics and biology relevant to applications of nanomaterials. The journal is devoted to reports of new and original experimental and theoretical research of an applied nature that integrate knowledge in the areas of materials, engineering, physics, bioscience, and chemistry into important applications of nanomaterials.
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