Masoumi-Dehghi Sajjad, Babashah Sadegh, Sadeghizadeh Majid
Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, P.O. Box: 14115-154, Tehran, Iran.
J Cell Commun Signal. 2020 Jun;14(2):233-244. doi: 10.1007/s12079-020-00548-5. Epub 2020 Feb 7.
Paracrine signaling between tumor and surrounding stromal cells is critical for the maintenance of tumor microenvironment during ovarian cancer progression. Small extracellular vesicles (sEVs; exosomes in particular) are nano-sized vesicles secreted actively by many cells including tumor cells and are found to have fundamental roles in intercellular communication through shuttling functional RNAs. Although microRNAs (also called miRNAs or miRs), small non-coding RNAs regulating gene expression, are selectively accumulated in tumor sEVs and can mediate intercellular communication, the exact biological mechanisms underlying the functions of exosomal miRNAs in ovarian tumor angiogenesis remain unclear. In this study, sEVs were isolated from conditioned medium of the human ovarian carcinoma cell line SKOV-3 using ExoQuick Exosome Precipitation Solution, and characterized by scanning electron microscopy, dynamic light scattering, and immunoblotting. To elucidate the possible paracrine effects on ovarian tumor cell-derived sEVs (TD-sEVs), we investigated the angiogenesis-related signaling events triggered by TD-sEVs in endothelial cells. Due to the possible role in ovarian tumor pathogenesis, we focused on miR-141-3p which was detected to be enriched in TD-sEVs compared with their corresponding donor cells. We identified that sEV transfer of miR-141-3p considerably reduced the expression levels of cytokine-inducible suppressors of cytokine signaling (SOCS)-5 leading to up-regulated JAK-STAT3 pathway in endothelial cells. We also observed that sEV-shuttled miR-141-3p may up-regulate the expression of VEGFR-2 in endothelial cells which leads to promoting endothelial cell migration and angiogenesis. The putative role of miR-141-3p shuttled by TD-sEVs in regulating VEGFR-2 expression was demonstrated by the ability of anti-miR-141-3p to rescue the promoting effects of TD-sEVs on the expression of VEGFR-2 in endothelial cells. Our results also revealed that TD-sEVs trigger the intracellular reactive oxygen species (ROS)-dependent activation of NF-κB signaling in endothelial cells. Taken together, our findings propose a novel model in which sEV transfer of epithelial ovarian cancer-secreted miR-141-3p plays as a significant mediator of intercellular communication, promoting endothelial cell angiogenesis.
肿瘤与周围基质细胞之间的旁分泌信号传导对于卵巢癌进展过程中肿瘤微环境的维持至关重要。小细胞外囊泡(特别是外泌体)是包括肿瘤细胞在内的许多细胞主动分泌的纳米级囊泡,并且发现其在通过转运功能性RNA进行细胞间通讯中具有重要作用。尽管微小RNA(也称为miRNA或miR)作为调节基因表达的小型非编码RNA,选择性地积累在肿瘤小细胞外囊泡中并可介导细胞间通讯,但外泌体miRNA在卵巢肿瘤血管生成中发挥功能的确切生物学机制仍不清楚。在本研究中,使用ExoQuick外泌体沉淀溶液从人卵巢癌细胞系SKOV-3的条件培养基中分离出小细胞外囊泡,并通过扫描电子显微镜、动态光散射和免疫印迹进行表征。为了阐明对卵巢肿瘤细胞衍生的小细胞外囊泡(TD-sEVs)可能的旁分泌作用,我们研究了TD-sEVs在内皮细胞中引发的血管生成相关信号事件。由于其在卵巢肿瘤发病机制中的可能作用,我们聚焦于miR-141-3p,与相应的供体细胞相比,其在TD-sEVs中被检测到富集。我们发现,miR-141-3p的小细胞外囊泡转移显著降低了细胞因子信号传导抑制因子(SOCS)-5的表达水平,导致内皮细胞中JAK-STAT3通路上调。我们还观察到,小细胞外囊泡转运的miR-141-3p可能上调内皮细胞中VEGFR-2的表达,从而促进内皮细胞迁移和血管生成。抗miR-141-3p能够挽救TD-sEVs对内皮细胞中VEGFR-2表达的促进作用,这证明了TD-sEVs转运的miR-141-3p在调节VEGFR-2表达中的假定作用。我们的结果还表明,TD-sEVs在内皮细胞中触发细胞内活性氧(ROS)依赖性的NF-κB信号激活。综上所述,我们的研究结果提出了一种新模型,其中上皮性卵巢癌分泌的miR-141-3p的小细胞外囊泡转移作为细胞间通讯的重要介质,促进内皮细胞血管生成。