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槟榔碱通过促进巨噬细胞分泌含miR-155-5p外泌体诱导人口腔成纤维细胞的活化
引用本文:黄永祺,喻 伟,游月华. 槟榔碱通过促进巨噬细胞分泌含miR-155-5p外泌体诱导人口腔成纤维细胞的活化[J]. 南方医科大学学报, 2023, 43(1): 60-67. DOI: 10.12122/j.issn.1673-4254.2023.01.08
作者姓名:黄永祺  喻 伟  游月华
作者单位:南方医科大学附属深圳市龙华人民医院口腔科,广东 深圳 518109;南方医科大学口腔医学院,广东 广州 510515
基金项目:国家自然基金青年项目(81901014);
摘    要:
目的 探讨槟榔碱(ARE)通过调控巨噬细胞外泌体内miR-155-5p水平诱导人口腔黏膜成纤维细胞向成纤维表型转化的作用机制。方法 以人单核细胞系(THP-1)与人口腔黏膜成纤维细胞系(HOMF)为研究对象。实验设为空白对照组、阴性对照组、ARE刺激组、ARE刺激后THP-1培养上清刺激组(CS)、ARE刺激后THP-1外泌体刺激组(EXO)、ARE刺激后THP-1无外泌体上清刺激组(NES)、miR-155-5p过表达组(miR-155-5p mimics)、ARE刺激后EXO处理对照组(NC+EXO-ARE)和miR-155-5p抑制联合ARE刺激后EXO处理(miR-155-5p inhibitor EXO-ARE)组。以流式细胞术检测THP-1细胞极化情况。Transwell细胞迁移实验检测HOMF细胞迁移能力。DCFH-DA检测细胞氧化应激水平。qRT-PCR检测细胞α-SMA、I型胶原和SOCS1的mRNA转录水平。免疫印迹实验检测细胞α-SMA、I型胶原与SOCS1蛋白表达。结果 流式检测显示,相较于对照组,ARE组THP-1细胞由M0趋向M1极化。ARE对THP-1和H...

关 键 词:槟榔碱  口腔黏膜下纤维化  外泌体  口腔成纤维细胞  巨噬细胞

Arecoline induces activation of human oral fibroblasts by promoting macrophage secretion of exosomes containing miR-155-5p
HUANG Yongqi,YU Wei,YOU Yuehua. Arecoline induces activation of human oral fibroblasts by promoting macrophage secretion of exosomes containing miR-155-5p[J]. Journal of Southern Medical University, 2023, 43(1): 60-67. DOI: 10.12122/j.issn.1673-4254.2023.01.08
Authors:HUANG Yongqi  YU Wei  YOU Yuehua
Affiliation:Department of Stomatology, Longhua People's Hospital Affiliated to Southern Medical University, Shenzhen 518109, China; School of Stomatology,Southern Medical University, Guangzhou 510515, China
Abstract:
Objective To investigate the mechanism by which arecoline regulates the level of miR-155-5p in macrophage-secreted exosomes to induce the transformation of human oral mucosal fibroblasts (HOMFs) into fibroblast phenotype. Methods Exosomes were harvested from human monocytic cell line THP-1 with or without arecoline treatment. The effects of arecoline-treated THP-1 cell culture supernatant (CS), THP-1-derived exosomes (EXO), exosome-depleted THP-1 cell supernatant (NES), miR-155-5p overexpression, and miR-155-5p inhibitor on migration ability of arecoline-treated HOMF cells were examined using Transwell migration assay. The polarization of THP-1 cells was detected using flow cytometry. DCFH-DA was used to detect the level of oxidative stress in the cells with different treatments. The mRNA and protein expressions ofα- SMA, type I collagen and SOCS1 in the cells were detected with qRT-PCR and Western blotting. Results Flow cytometry showed that arecoline- treated THP-1 cells exhibited obvious polarization from M0 to M1. Both the supernatant and exosomes from arecoline-treated THP-1 cells significantly enhanced the migration ability of HOMF cells, increased intracellular oxidative stress, up-regulated the expressions of miR-155- 5p and the mRNA and protein levels of α-SMA and type I collagen, and lowered the mRNA and protein expressions of SOCS1. In HOMF cells treated with exosomes from arecoline- treated THP-1 cells, overexpression of miR-155-5p significantly enhanced cell migration ability and increased cellular expressions of α-SMA and type I collagen, and miR-155-5p inhibitor caused the opposite changes. Conclusion Arecoline can up-regulate miR-155-5p expression in THP-1 cells and inhibit the expression of SOCS1 protein in HOMF cells via the exosome pathway, thus promoting the fibrotic phenotype transformation of HOMF cells.
Keywords:arecoline   oral submucosal fibrosis   exosome   oral fibroblasts   macrophages,
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