Li Dandan, Li Jian
Department of Family Planning, Beijing Obstetrics and Gynecology Hospital, Capital Medical Universityy, Beijing, China (mainland).
Med Sci Monit. 2016 Mar 21;22:922-9. doi: 10.12659/msm.895459.
The specific causes of recurrent spontaneous abortion (RSA) remain unknown in 37-79% of affected women. The aim of this study was to explore the expression levels of 6 miRNAs in natural killer (NK) cells from the decidua of patients with unexplained RSA (URSA) and to predict the target genes of 3 miRNAs.
MATERIAL/METHODS: Two groups were examined: URSA (n=20) and controls (n=20). Flow cytometry analysis was used to identify NK cells isolated from the decidua. Transcriptional levels of miRNA were monitored using quantitative real-time reverse transcription-polymerase chain reaction. Prediction and analysis of mRNA targets of differentially expressed miRNAs were performed using bioinformatics methods.
Five miRNAs [miR-34a (+281%, P<0.001), miR-155 (+396%, P<0.001), miR-141 (+142%, P<0.01), miR-125a (+279%, P<0.001), and miR-125b (+185%, P<0.001)] were up-regulated, while miR-24 was down-regulated (-64%, P<0.01) in the URSA group, compared to the control group. This study identified potential miRNA targets: miR-34a-3p/5p, 585/1718 (targets of miR-34a-3p/targets of miR-34a-5p), miR-141-3p/5p, 2270/629 (targets of miR-141-3p/targets of miR-141-5p), and miR-24, 2320 target genes. A total of 140 pathways related to target genes were identified including PI3K-Akt, focal adhesion, MAPK, Wnt, regulation of the actin cytoskeleton, T cell receptor, TGF-β, and estrogen signaling pathways.
This study suggests that miR-34a-3p/5p, miR-141-3p/5p, and miR-24 in decidual NK cells could be associated with URSA. These findings might contribute to the panel of diagnostic and prognostic biomarkers with clinical utility, and facilitate the development of new strategies for targeted therapy against URSA.
在37%-79%的复发性自然流产(RSA)女性患者中,其具体病因仍不明。本研究旨在探讨不明原因复发性流产(URSA)患者蜕膜中自然杀伤(NK)细胞中6种微小RNA(miRNA)的表达水平,并预测其中3种miRNA的靶基因。
材料/方法:研究对象分为两组:URSA组(n = 20)和对照组(n = 20)。采用流式细胞术分析鉴定从蜕膜中分离出的NK细胞。使用定量实时逆转录-聚合酶链反应监测miRNA的转录水平。采用生物信息学方法对差异表达miRNA的mRNA靶标进行预测和分析。
与对照组相比,URSA组中有5种miRNA [miR-34a(上调281%,P < 0.001)、miR-155(上调396%,P < 0.001)、miR-141(上调142%,P < 0.01)、miR-125a(上调279%,P < 0.001)和miR-125b(上调185%,P < 0.001)]表达上调,而miR-24表达下调(下调64%,P < 0.01)。本研究鉴定出潜在的miRNA靶标:miR-34a-3p/5p、585/1718(miR-34a-3p的靶标/miR-34a-5p的靶标)、miR-141-3p/5p、2270/629(miR-141-3p的靶标/miR-141-5p的靶标)以及miR-24的2320个靶基因。共鉴定出140条与靶基因相关的信号通路,包括PI3K-Akt、粘着斑、丝裂原活化蛋白激酶(MAPK)、Wnt、肌动蛋白细胞骨架调节、T细胞受体、转化生长因子-β(TGF-β)和雌激素信号通路。
本研究表明,蜕膜NK细胞中的miR-34a-3p/5p、miR-141-3p/5p和miR-24可能与URSA有关。这些发现可能有助于建立具有临床应用价值的诊断和预后生物标志物组合,并促进针对URSA的靶向治疗新策略的开发。