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H19 通过竞争性结合 let-7 来调节滋养层细胞球的黏附。

H19 regulates trophoblastic spheroid adhesion by competitively binding to let-7.

机构信息

Reproductive Medicine Center, Xiangya Hospital, Central South University, Changsha, China.

Department of Obstetrics and Gynecology, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Reproduction. 2019 May;157(5):423-430. doi: 10.1530/REP-18-0339.

Abstract

Integrin β3 (ITGB3), which is the target gene of the miRNA let-7 that can be antagonized by long noncoding RNA (lncRNA) H19, is well known to have a critical role in endometrium receptivity. However, the regulation of ITGB3 in cell-cell or cell-extracellular matrix adhesion and invasion for the maintenance of early pregnancy remains unknown. This study aimed to explore the role of the H19/let-7/ITGB3 axis in regulating trophoblastic spheroid adhesion and in vitro invasion ability using the HTR-8/SVneo cell line and to investigate the expression levels of lncRNA H19 and ITGB3 in human products of conception. The in vitro knockdown of H19 resulted in decreased expression of ITGB3 at the mRNA and protein levels and reduced the adhesion and invasion ability. In the embryonic chorion tissue of spontaneous abortion (SA), the expressions of H19 and ITGB3 at both the mRNA and protein levels decreased. The results of quantitative RT-PCR, Western blot analysis, dual-luciferase report gene and functional miRNA let-7 rescue experiments, adhesion assay and in vitro transwell invasion assay confirmed that H19 regulated trophoblastic spheroid adhesion with endometrial stromal cells through the H19/let-7/ITGB3 axis, thereby providing an improved understanding of the molecular mechanism of SA.

摘要

整合素β 3(ITGB3)是 miRNA let-7 的靶基因,而 let-7 可被长链非编码 RNA(lncRNA)H19 拮抗,其在子宫内膜容受性中起着关键作用。然而,H19/let-7/ITGB3 轴在维持早期妊娠的细胞-细胞或细胞-细胞外基质黏附和侵袭中的调控作用尚不清楚。本研究旨在通过 HTR-8/SVneo 细胞系探讨 H19/let-7/ITGB3 轴在调节滋养层细胞球黏附和体外侵袭能力中的作用,并研究人妊娠产物中 lncRNA H19 和 ITGB3 的表达水平。体外敲低 H19 导致 ITGB3 在 mRNA 和蛋白水平的表达降低,并降低了黏附和侵袭能力。在自发性流产(SA)的胚胎绒毛组织中,H19 和 ITGB3 的表达在 mRNA 和蛋白水平均降低。定量 RT-PCR、Western blot 分析、双荧光素酶报告基因和功能 miRNA let-7 挽救实验、黏附实验和体外 Transwell 侵袭实验证实,H19 通过 H19/let-7/ITGB3 轴调节滋养层细胞球与子宫内膜基质细胞的黏附,从而为深入了解 SA 的分子机制提供了依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c1c2/6433002/1e11a7f647ce/REP-18-0339fig1.jpg

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