Department of Obstetrics and Gynecology, Medicine Center for Human Reproduction, Zhongnan Hospital of Wuhan University.
Clinical Medicine Research Centre of Prenatal Diagnosis and Birth Health in Hubei Province, Wuhan, China.
J Hypertens. 2022 May 1;40(5):1030-1041. doi: 10.1097/HJH.0000000000003112. Epub 2022 Feb 23.
Preeclampsia is one of the most important complications during pregnancy and the leading cause of maternal morbidity and mortality; however, the pathogenesis of preeclampsia remains partially misunderstood. The aim of this study was to identify placenta-derived exosomal microRNAs (miRNAs) involved in the preeclampsia process.
Peripheral blood was collected from normal and preeclampsia pregnant women, and placenta-derived exosomes were extracted. Small RNA sequencing was performed to identify the exosomal miRNAs involved in preeclampsia. The function of a differentially expressed exosomal miRNA was verified.
The extracted exosomes presented round or ovallike structures with diameters of approximately 80 nm and could be recognized by antibodies against CD9, CD81, and placental alkaline phosphatase. A total of 1013 exosomal miRNAs were identified by small RNA sequencing, of which 946 were known miRNAs and 67 were novel miRNAs. Twenty-six miRNAs were identified as differentially expressed when comparing the data of the preeclampsia and normal groups. One of the differentially expressed miRNAs, hsa-miR-370-3p, which was upregulated in the preeclampsia group, was shown to bind to the 3' untranslated region of C-X-C motif chemokine 12, a chemokine that plays important role during preeclampsia process. Moreover, functional analysis revealed that hsamiR-370-3p could inhibit proliferation, migration, and invasion while promoting apoptosis of HTR-8/SVneo cells.
A total of 1013 placenta-derived exosomal miRNAs were identified by small RNA sequencing, of which 26 were differentially expressed. The function of one differentially expressed miRNA (hsa-miR-370-3p) was verified. Our results provide new perspectives on the pathogenesis of preeclampsia and potential biomarkers for preeclampsia diagnosis.
子痫前期是妊娠期间最重要的并发症之一,也是孕产妇发病率和死亡率的主要原因;然而,子痫前期的发病机制仍部分未被理解。本研究旨在鉴定参与子痫前期过程的胎盘来源的外泌体 microRNAs(miRNAs)。
采集正常和子痫前期孕妇的外周血,并提取胎盘来源的外泌体。进行小 RNA 测序以鉴定参与子痫前期的外泌体 miRNAs。验证差异表达的外泌体 miRNA 的功能。
提取的外泌体呈现出直径约为 80nm 的圆形或椭圆形结构,并用针对 CD9、CD81 和胎盘碱性磷酸酶的抗体可识别。通过小 RNA 测序共鉴定出 1013 个外泌体 miRNAs,其中 946 个是已知的 miRNAs,67 个是新的 miRNAs。在比较子痫前期组和正常组的数据时,鉴定出 26 个 miRNA 存在差异表达。其中,在子痫前期组中上调的差异表达 miRNA 之一 hsa-miR-370-3p,被证明与趋化因子 C-X-C 基序 12 的 3'非翻译区结合,该趋化因子在子痫前期过程中发挥重要作用。此外,功能分析表明 hsa-miR-370-3p 可抑制 HTR-8/SVneo 细胞的增殖、迁移和侵袭,同时促进其凋亡。
通过小 RNA 测序共鉴定出 1013 个胎盘来源的外泌体 miRNAs,其中 26 个存在差异表达。验证了一个差异表达 miRNA(hsa-miR-370-3p)的功能。我们的研究结果为子痫前期的发病机制提供了新的视角,并为子痫前期的诊断提供了潜在的生物标志物。