Clin Lab. 2023 Feb 1;69(2). doi: 10.7754/Clin.Lab.2022.220430.
The goal of this study was to screen for differentially expressed exosomal miRNAs in peripheral blood samples of early-onset preeclampsia and normal pregnant patients using high-throughput sequencing methods and explore their effects on the pathogenesis of preeclampsia.
Peripheral blood samples from 5 patients with early-onset preeclampsia and 5 normal pregnant women (control group) were enrolled. Then, exosomes were extracted from each sample, and the procedure was replicated three times. An Illumina HiSeq4000 sequencing platform was used to analyze exosomal miRNAs in all samples before comparison. The target genes and signaling pathway predictions and the biological function enrichments of significant and differentially expressed miRNAs were assessed using Miranda and Starbase software, as well as GO and KEGG databases.
Compared with the control, patients in the early-onset preeclampsia group had 65 significantly and differentially expressed exosomal miRNAs in their peripheral blood samples. The results have shown that of the 65 differentially expressed miRNAs, 17, including has-miR-6855, has-miR-7151, and has-miR-6777, were up-regulated, and 48, including has-miR-1247, has-miR-29B2, and has-miR-941, were down-regulated (p < 0.05). The Miranda and TargetScanS algorithms predicted a total of 2,231 target genes from the differentially expressed miRNAs. The Go and KEGG analyses showed that the principal biological function of these target genes was the regulation of Ras protein signal transduction, histone modification, GTPase-mediated signal transduction, and transforming growth factor (TGF)-β. Additionally, the results also showed that the major pathways involved in the regulation of these functions were the PI3K Akt, MAPK, tumor necrosis factor, and EGFR tyrosine kinase inhibition signaling pathways.
There are significant differences in the expression profiles of exosomal miRNAs between early-onset preeclampsia patients and normal pregnant women. These differentially expressed miRNAs may not only play an important regulatory role in the occurrence of early-onset preeclampsia but also participate in its pathophysiological process through genetic regulation of a variety of biological functions and signal pathways.
本研究旨在通过高通量测序方法筛选早发型子痫前期患者和正常孕妇外周血样本中差异表达的外泌体 miRNAs,并探讨其对子痫前期发病机制的影响。
纳入 5 例早发型子痫前期患者和 5 例正常孕妇(对照组)的外周血样本,提取外泌体,每个样本重复提取 3 次,然后使用 Illumina HiSeq4000 测序平台对所有样本进行测序分析,比较后进行差异分析。采用 Miranda 和 Starbase 软件以及 GO 和 KEGG 数据库对差异显著的 miRNA 的靶基因和信号通路预测以及生物功能富集进行评估。
与对照组相比,早发型子痫前期组患者外周血样本中差异表达的外泌体 miRNAs 有 65 个。结果表明,在 65 个差异表达的 miRNAs 中,有 17 个上调,包括 has-miR-6855、has-miR-7151 和 has-miR-6777,有 48 个下调,包括 has-miR-1247、has-miR-29B2 和 has-miR-941(p<0.05)。Miranda 和 TargetScanS 算法从差异表达的 miRNAs 中共预测了 2231 个靶基因。GO 和 KEGG 分析表明,这些靶基因的主要生物学功能是 Ras 蛋白信号转导、组蛋白修饰、GTPase 介导的信号转导和转化生长因子(TGF)-β的调节。此外,结果还表明,这些功能调节的主要途径是 PI3K-Akt、MAPK、肿瘤坏死因子和 EGFR 酪氨酸激酶抑制信号通路。
早发型子痫前期患者和正常孕妇的外泌体 miRNAs 表达谱存在显著差异。这些差异表达的 miRNAs 不仅可能在早发型子痫前期的发生中发挥重要的调节作用,而且可能通过对多种生物功能和信号通路的遗传调节参与其病理生理过程。