Reproductive Medicine Centre, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Reproductive Medicine Centre, The Affiliated Yantai Yuhuangding Hospital of Qingdao University, Yantai, China.
Reprod Biomed Online. 2020 May;40(5):627-636. doi: 10.1016/j.rbmo.2020.01.018. Epub 2020 Jan 30.
Repeated implantation failure (RIF) is a major limiting factor in assisted reproductive technology. As miR-145 (also known as MIR145) is up-regulated in patients with RIF, this study asked, what is the molecular mechanism underlying the affect of miR-145 on embryo implantation in RIF?
Ishikawa cells were infected with lentivirus containing miR-145 and miR-145 NC. Massive transcriptome data analyses and bioinformatics analysis were used to search for a potential candidate target of miR-145. The expression of the potential candidate target was detected using quantitative reverse transcription PCR (qRT-PCR) and western blotting in the Ishikawa cells infected with lentivirus containing miR-145 or miR-145 NC. Subsequently, a dual luciferase reporter assay was performed to verify whether the potential candidate target was a novel direct target of miR-145. In addition, expression of PAI-1 (plasminogen activator inhibitor 1, also known as SERPINE1) in endometrial tissue from women with RIF and in control endometrial tissue was examined using qRT-PCR and immunohistochemistry.
Based on massive transcriptome data analyses and bioinformatics analysis, PAI-1 was regarded as a potential candidate target of miR-145. miR-145 overexpression was achieved in Ishikawa cells. PAI-1 was confirmed as a direct target of miR-145 by bioinformatic analysis, qRT-PCR, western blotting and dual luciferase reporter assay. Further, results from the clinical sample indicated that at both the mRNA and protein levels, PAI-1 expression was down-regulated in endometrial tissues from women with RIF compared with control group women, and this was negatively related to miR-145 expression.
The study results suggests that miR-145 may target and down-regulate PAI-1 expression and influence embryo implantation in women with RIF who are undergoing IVF.
反复着床失败(RIF)是辅助生殖技术的主要限制因素。由于 miR-145(也称为 MIR145)在 RIF 患者中上调,因此本研究探讨了 miR-145 影响 RIF 胚胎着床的分子机制。
用携带 miR-145 和 miR-145 NC 的慢病毒感染 Ishikawa 细胞。使用大规模转录组数据分析和生物信息学分析来搜索 miR-145 的潜在候选靶标。用携带 miR-145 或 miR-145 NC 的慢病毒感染 Ishikawa 细胞,检测潜在候选靶标的表达情况。随后,进行双荧光素酶报告基因检测以验证潜在候选靶标是否为 miR-145 的新型直接靶标。此外,使用 qRT-PCR 和免疫组化检测 RIF 患者和对照组子宫内膜组织中 PAI-1(纤溶酶原激活物抑制剂 1,也称为 SERPINE1)的表达。
基于大规模转录组数据分析和生物信息学分析,将 PAI-1 视为 miR-145 的潜在候选靶标。在 Ishikawa 细胞中实现了 miR-145 的过表达。通过生物信息学分析、qRT-PCR、western blot 和双荧光素酶报告基因检测证实了 PAI-1 是 miR-145 的直接靶标。进一步的临床样本结果表明,在 RIF 患者和对照组患者的子宫内膜组织中,PAI-1 的表达均下调,且与 miR-145 的表达呈负相关。
研究结果表明,miR-145 可能靶向并下调 PAI-1 的表达,影响接受 IVF 的 RIF 患者的胚胎着床。