关翰, 孙文衍, 汪盛, 陈志军. M2型巨噬细胞外泌体包裹miR-374a促进前列腺癌恶性进展的机制研究[J]. 蚌埠医科大学学报, 2023, 48(6): 701-711. DOI: 10.13898/j.cnki.issn.1000-2200.2023.06.001
    引用本文: 关翰, 孙文衍, 汪盛, 陈志军. M2型巨噬细胞外泌体包裹miR-374a促进前列腺癌恶性进展的机制研究[J]. 蚌埠医科大学学报, 2023, 48(6): 701-711. DOI: 10.13898/j.cnki.issn.1000-2200.2023.06.001
    GUAN Han, SUN Wen-yan, WANG Sheng, CHEN Zhi-jun. Mechanism of miR-374a encapsulation in M2 macrophage exosomes promotes malignant progression of prostate cancer[J]. Journal of Bengbu Medical University, 2023, 48(6): 701-711. DOI: 10.13898/j.cnki.issn.1000-2200.2023.06.001
    Citation: GUAN Han, SUN Wen-yan, WANG Sheng, CHEN Zhi-jun. Mechanism of miR-374a encapsulation in M2 macrophage exosomes promotes malignant progression of prostate cancer[J]. Journal of Bengbu Medical University, 2023, 48(6): 701-711. DOI: 10.13898/j.cnki.issn.1000-2200.2023.06.001

    M2型巨噬细胞外泌体包裹miR-374a促进前列腺癌恶性进展的机制研究

    Mechanism of miR-374a encapsulation in M2 macrophage exosomes promotes malignant progression of prostate cancer

    • 摘要:
      目的探究M2型巨噬细胞外泌体包裹miR-374a对前列腺癌(prostate cancer, PCa)恶性进展的影响并探讨其分子机制。
      方法在成功建立M2型巨噬细胞的基础上,抽提并鉴定其外泌体,检测外泌体中差异表达的miRNA,同时在不同PCa细胞中验证,选取miR-374a进行研究;M2细胞中转染cy3荧光标记的miR-374a与PC3细胞共培养,荧光显微镜观察PC3细胞中cy3荧光表达情况;DU145和PC3细胞中转染miR-374a inhibitor进行增殖、迁移等细胞功能学实验及裸鼠皮下成瘤实验;通过数据库筛选叉头盒转录因子(FOXO1)作为靶基因,通过Western blotting、荧光素酶报告基因实验及免疫荧光实验进行验证;干扰FOXO1后进行细胞功能学实验,观察是否能逆转miR-374a inhibitor对DU145及PC3细胞功能学的影响。
      结果成功建立M2细胞并抽提其外泌体,其中miR-374a在M2细胞外泌体中高表达;荧光定量PCR实验结果证明miR-374a在PC3及DU145中表达量显著高于LNCaP,在M2细胞中表达量高于THP-1细胞,PC3细胞与M2细胞共培养后,M2细胞可通过外泌体传递miR-374a至PC3细胞内;敲低PC3和DU145细胞中miR-374a的表达量后显著降低其增殖、迁移能力并促进其凋亡,在PC3中敲低miR-374a表达后裸鼠皮下成瘤体积显著减小;Western blotting、荧光素酶报告基因实验及免疫荧光实验结果证明miR-374a可以直接结合FOXO1,抑制β-catenin入核并抑制PCa细胞EMT;挽救实验结果说明转染si-FOXO1后可逆转miR-374a对PC3和DU145细胞迁移的抑制作用。
      结论M2细胞可通过外泌体传递miR-374a进入PCa细胞靶向FOXO1抑制其恶性进展。

       

      Abstract:
      ObjectiveTo explore the effect of miR-374a encapsulated by M2 macrophage exosomes on the malignant progression of prostate cancer(PCa) and explore its molecular mechanism.
      MethodsBased on the successful establishment of M2 macrophages, the exosomes were extracted and identified, and the differentially expressed miRNAs in exosomes were detected. MiR-374a was verified in different PCa cells; M2 cells transfected with cy3 fluorescently labeled miR-374a were cocultured with PC3 cells, and the expression of cy3 fluorescence in PC3 cells was observed by fluorescence microscope; DU145 and PC3 cells were transfected with miR-374a inhibitor for cell function experiments. Forkhead box O1(FOXO1) was selected as the target gene through the database, which was verified by Western blotting, luciferase reporter gene assay and immunofluorescence experiment; after interfering with FOXO1, cell function experiments were carried out to observe whether miR-374a inhibitor could reverse the effects on DU145 and PC3 cells.
      ResultsM2 cells were successfully established and their exosomes were extracted, and miR-374a was highly expressed in the exosomes of M2 cells; the results of fluorescence quantitative PCR showed that the expression of miR-374a in PC3 and DU145 cells was significantly higher than that in LNCaP cells, and the expression in M2 cells was higher than that in THP-1 cells. After co culture of PC3 cells and M2 cells, M2 cells could transmit miR-374a to PC3 cells through exosomes; knockdown of miR-374a expression in PC3 and DU145 cells significantly reduced their proliferation, migration ability and promoted their apoptosis. Knockdown of miR-374a expression in PC3 significantly reduced the subcutaneous tumor formation volume of nude mice; the results of Western blotting, luciferase reporter gene assay and immunofluorescence assay demonstrated that miR-374a could directly bind to FOXO1 and inhibit β-catenin enters nucleus and inhibits EMT in PCa cells; the results of rescue experiment showed that transfection of si-FOXO1 could reverse the inhibitory effect of miR-374a on the migration of PC3 and DU145 cells.
      ConclusionsM2 cells can deliver miR-374a into PCa cells through exosomes to target FOXO1 and inhibit its malignant progression.

       

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